geneid | 4330 |
---|---|
ensemblid | ENSG00000169184.7 |
hgncid | 7180 |
symbol | MN1 |
name | MN1 proto-oncogene, transcriptional regulator |
refseq_nuc | NM_002430.3 |
refseq_prot | NP_002421.3 |
ensembl_nuc | ENST00000302326.5 |
ensembl_prot | ENSP00000304956.4 |
mane_status | MANE Select |
chr | chr22 |
start | 27748277 |
end | 27801756 |
strand | - |
ver | v1.2 |
region | chr22:27748277-27801756 |
region5000 | chr22:27743277-27806756 |
regionname0 | MN1_chr22_27748277_27801756 |
regionname5000 | MN1_chr22_27743277_27806756 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1320 | 317 | 68 | 64 | 138 | 13 | 32 | 103 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0002 | 0/0 | 1321 | 49 | 18 | 10 | 15 | 4 | 2 | 9 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0003 | 0/0 | 1318 | 12 | 5 | 3 | 4 | 0 | 0 | 3 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0004 | 0/0 | 1320 | 5 | 0 | 3 | 0 | 1 | 1 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0005 | 0/0 | 1319 | 3 | 2 | 0 | 0 | 0 | 1 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0006 | 0/0 | 1320 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0007 | 0/0 | 1326 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0008 | 0/0 | 1320 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0009 | 0/0 | 1321 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0010 | 0/0 | 1320 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0011 | 0/0 | 1320 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0012 | 0/0 | 1320 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0013 | 0/0 | 1320 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 3963 | 286 | 44 | 62 | 133 | 13 | 32 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
c0002 | 0/0 | 3966 | 29 | 1 | 8 | 14 | 4 | 2 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
c0003 | 0/0 | 3966 | 14 | 12 | 2 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
c0004 | 0/0 | 3957 | 12 | 5 | 3 | 4 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
c0005 | 0/0 | 3963 | 10 | 8 | 2 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
c0006 | 0/0 | 3966 | 5 | 5 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
c0007 | 0/0 | 3963 | 5 | 0 | 3 | 0 | 1 | 1 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
c0008 | 0/0 | 3963 | 4 | 4 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
c0009 | 0/0 | 3963 | 4 | 4 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
c0010 | 0/0 | 3963 | 3 | 3 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
c0011 | 0/0 | 3960 | 3 | 2 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
c0012 | 0/0 | 3963 | 3 | 0 | 0 | 3 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
c0013 | 0/0 | 3963 | 2 | 2 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
c0014 | 0/0 | 3963 | 2 | 2 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
c0015 | 0/0 | 3963 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
c0016 | 0/0 | 3963 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
c0017 | 0/0 | 3963 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
c0018 | 0/0 | 3963 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
c0019 | 0/0 | 3963 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
c0020 | 0/0 | 3966 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
c0021 | 0/0 | 3963 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
c0022 | 0/0 | 3966 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
c0023 | 0/0 | 3963 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
c0024 | 0/0 | 3963 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
c0025 | 0/0 | 3981 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
c0026 | 0/0 | 3963 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 3852 | 85 | 8 | 26 | 31 | 3 | 15 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
t0002 | 0/0 | 3853 | 72 | 22 | 21 | 16 | 5 | 8 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
t0003 | 0/0 | 3852 | 32 | 0 | 2 | 27 | 0 | 3 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
t0004 | 0/0 | 3853 | 27 | 0 | 4 | 17 | 4 | 2 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
t0005 | 0/0 | 3852 | 17 | 0 | 5 | 10 | 1 | 1 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
t0006 | 0/0 | 3852 | 12 | 2 | 1 | 8 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
t0007 | 0/0 | 3851 | 12 | 2 | 1 | 9 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
t0008 | 0/0 | 3853 | 9 | 0 | 2 | 0 | 3 | 4 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
t0009 | 0/0 | 3874 | 7 | 6 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
t0010 | 0/0 | 3852 | 6 | 0 | 0 | 5 | 1 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
t0011 | 0/0 | 3853 | 5 | 0 | 0 | 5 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
t0012 | 0/0 | 3851 | 5 | 0 | 0 | 5 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
t0013 | 0/0 | 3853 | 5 | 0 | 0 | 5 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
t0014 | 0/0 | 3873 | 4 | 3 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
t0015 | 0/0 | 3872 | 4 | 4 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
t0016 | 0/0 | 3852 | 4 | 4 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
t0017 | 0/0 | 3853 | 4 | 0 | 4 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
t0018 | 0/0 | 3852 | 4 | 4 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
t0019 | 0/0 | 3874 | 3 | 2 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
t0020 | 0/0 | 3853 | 3 | 0 | 1 | 2 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
t0021 | 0/0 | 3854 | 3 | 3 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
t0022 | 0/0 | 3852 | 3 | 0 | 0 | 3 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
t0023 | 0/0 | 3873 | 2 | 2 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
t0024 | 0/0 | 3873 | 2 | 1 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
t0025 | 0/0 | 3873 | 2 | 1 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
t0026 | 0/0 | 3853 | 2 | 0 | 0 | 2 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
t0027 | 0/0 | 3852 | 2 | 0 | 2 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
t0028 | 0/0 | 3852 | 2 | 2 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
t0029 | 0/0 | 3852 | 2 | 0 | 2 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
t0030 | 0/0 | 3853 | 2 | 0 | 1 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
t0031 | 0/0 | 3853 | 2 | 0 | 2 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
t0032 | 0/0 | 3852 | 2 | 0 | 0 | 0 | 0 | 2 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
t0033 | 0/0 | 3854 | 2 | 2 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
t0034 | 0/0 | 3853 | 2 | 0 | 0 | 2 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
t0035 | 0/0 | 3850 | 2 | 2 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
t0036 | 0/0 | 3874 | 2 | 2 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
t0037 | 0/0 | 3852 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
t0038 | 0/0 | 3853 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
t0039 | 0/0 | 3874 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
t0040 | 0/0 | 3874 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
t0041 | 0/0 | 3873 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
t0042 | 0/0 | 3872 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
t0043 | 0/0 | 3873 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
t0044 | 0/0 | 3872 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
t0045 | 0/0 | 3873 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
t0046 | 0/0 | 3872 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
t0047 | 0/0 | 3851 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
t0048 | 0/0 | 3851 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
t0049 | 0/0 | 3853 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
t0050 | 0/0 | 3853 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
t0051 | 0/0 | 3853 | 1 | 0 | 0 | 0 | 1 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
t0052 | 0/0 | 3853 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
t0053 | 0/0 | 3852 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
t0054 | 0/0 | 3852 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
t0055 | 0/0 | 3852 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
t0056 | 0/0 | 3851 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
t0057 | 0/0 | 3852 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
t0058 | 0/0 | 3852 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
t0059 | 0/0 | 3852 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
t0060 | 0/0 | 3853 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
t0061 | 0/0 | 3854 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
t0062 | 0/0 | 3853 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
t0063 | 0/0 | 3851 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
t0064 | 0/0 | 3853 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
t0065 | 0/0 | 3853 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
t0066 | 0/0 | 3853 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
t0067 | 0/0 | 3853 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
t0068 | 0/0 | 3852 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
t0069 | 0/0 | 3851 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
t0070 | 0/0 | 3851 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
t0071 | 0/0 | 3873 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
t0072 | 0/0 | 3873 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
t0073 | 0/0 | 3873 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
t0074 | 0/0 | 3851 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
t0075 | 0/0 | 3852 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
t0076 | 0/0 | 3854 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0007 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0101 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0227 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0308 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0366 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0367 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0370 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0372 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0382 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0383 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0384 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0385 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
g0386 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 3963 | 286 | 44 | 62 | 133 | 13 | 32 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0005 | 0/0 | 3963 | 10 | 8 | 2 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0008 | 0/0 | 3963 | 4 | 4 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0009 | 0/0 | 3963 | 4 | 4 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0010 | 0/0 | 3963 | 3 | 3 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0012 | 0/0 | 3963 | 3 | 0 | 0 | 3 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0013 | 0/0 | 3963 | 2 | 2 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0014 | 0/0 | 3963 | 2 | 2 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0016 | 0/0 | 3963 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0019 | 0/0 | 3963 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0021 | 0/0 | 3963 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0002c0002 | 0/0 | 3966 | 29 | 1 | 8 | 14 | 4 | 2 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0002c0003 | 0/0 | 3966 | 14 | 12 | 2 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0002c0006 | 0/0 | 3966 | 5 | 5 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0002c0020 | 0/0 | 3966 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0003c0004 | 0/0 | 3957 | 12 | 5 | 3 | 4 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0004c0007 | 0/0 | 3963 | 5 | 0 | 3 | 0 | 1 | 1 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0005c0011 | 0/0 | 3960 | 3 | 2 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0006c0026 | 0/0 | 3963 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0007c0025 | 0/0 | 3981 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0008c0023 | 0/0 | 3963 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0009c0022 | 0/0 | 3966 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0010c0015 | 0/0 | 3963 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0011c0017 | 0/0 | 3963 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0012c0018 | 0/0 | 3963 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0013c0024 | 0/0 | 3963 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 7814 | 68 | 6 | 20 | 24 | 2 | 14 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0001t0002 | 0/0 | 7815 | 58 | 15 | 19 | 13 | 5 | 6 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0001t0003 | 0/0 | 7814 | 27 | 0 | 1 | 24 | 0 | 2 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0001t0004 | 0/0 | 7815 | 20 | 0 | 4 | 15 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0001t0005 | 0/0 | 7814 | 10 | 0 | 5 | 4 | 1 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0001t0006 | 0/0 | 7814 | 9 | 1 | 0 | 8 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0001t0007 | 0/0 | 7813 | 8 | 1 | 0 | 7 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0001t0008 | 0/0 | 7815 | 8 | 0 | 1 | 0 | 3 | 4 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0001t0009 | 0/0 | 7836 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0001t0010 | 0/0 | 7814 | 6 | 0 | 0 | 5 | 1 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0001t0011 | 0/0 | 7815 | 5 | 0 | 0 | 5 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0001t0012 | 0/0 | 7813 | 5 | 0 | 0 | 5 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0001t0013 | 0/0 | 7815 | 5 | 0 | 0 | 5 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0001t0016 | 0/0 | 7814 | 2 | 2 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0001t0017 | 0/0 | 7815 | 2 | 0 | 2 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0001t0020 | 0/0 | 7815 | 2 | 0 | 1 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0001t0021 | 0/0 | 7816 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0001t0022 | 0/0 | 7814 | 3 | 0 | 0 | 3 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0001t0023 | 0/0 | 7835 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0001t0024 | 0/0 | 7835 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0001t0025 | 0/0 | 7835 | 2 | 1 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0001t0026 | 0/0 | 7815 | 2 | 0 | 0 | 2 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0001t0027 | 0/0 | 7814 | 2 | 0 | 2 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0001t0028 | 0/0 | 7814 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0001t0029 | 0/0 | 7814 | 2 | 0 | 2 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0001t0030 | 0/0 | 7815 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0001t0031 | 0/0 | 7815 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0001t0032 | 0/0 | 7814 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0001t0033 | 0/0 | 7816 | 2 | 2 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0001t0034 | 0/0 | 7815 | 2 | 0 | 0 | 2 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0001t0037 | 0/0 | 7814 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0001t0044 | 0/0 | 7834 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0001t0045 | 0/0 | 7835 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0001t0046 | 0/0 | 7834 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0001t0047 | 0/0 | 7813 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0001t0050 | 0/0 | 7815 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0001t0051 | 0/0 | 7815 | 1 | 0 | 0 | 0 | 1 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0001t0052 | 0/0 | 7815 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0001t0053 | 0/0 | 7814 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0001t0054 | 0/0 | 7814 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0001t0055 | 0/0 | 7814 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0001t0056 | 0/0 | 7813 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0001t0057 | 0/0 | 7814 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0001t0058 | 0/0 | 7814 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0001t0059 | 0/0 | 7814 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0001t0060 | 0/0 | 7815 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0001t0061 | 0/0 | 7816 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0001t0062 | 0/0 | 7815 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0001t0063 | 0/0 | 7813 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0001t0064 | 0/0 | 7815 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0001t0065 | 0/0 | 7815 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0001t0066 | 0/0 | 7815 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0001t0067 | 0/0 | 7815 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0001t0068 | 0/0 | 7814 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0001t0069 | 0/0 | 7813 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0001t0074 | 0/0 | 7813 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0001t0075 | 0/0 | 7814 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0001t0076 | 0/0 | 7816 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0005t0002 | 0/0 | 7815 | 3 | 3 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0005t0006 | 0/0 | 7814 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0005t0009 | 0/0 | 7836 | 2 | 1 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0005t0016 | 0/0 | 7814 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0005t0028 | 0/0 | 7814 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0005t0043 | 0/0 | 7835 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0005t0049 | 0/0 | 7815 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0008t0018 | 0/0 | 7814 | 2 | 2 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0008t0035 | 0/0 | 7812 | 2 | 2 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0009t0002 | 0/0 | 7815 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0009t0006 | 0/0 | 7814 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0009t0021 | 0/0 | 7816 | 2 | 2 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0010t0014 | 0/0 | 7835 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0010t0024 | 0/0 | 7835 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0010t0040 | 0/0 | 7836 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0012t0001 | 0/0 | 7814 | 2 | 0 | 0 | 2 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0012t0020 | 0/0 | 7815 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0013t0001 | 0/0 | 7814 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0013t0048 | 0/0 | 7813 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0014t0018 | 0/0 | 7814 | 2 | 2 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0016t0003 | 0/0 | 7814 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0019t0004 | 0/0 | 7815 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0001c0021t0007 | 0/0 | 7813 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0002c0002t0001 | 0/0 | 7817 | 6 | 0 | 2 | 4 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0002c0002t0002 | 0/0 | 7818 | 3 | 0 | 1 | 2 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0002c0002t0003 | 0/0 | 7817 | 3 | 0 | 1 | 1 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0002c0002t0004 | 0/0 | 7818 | 5 | 0 | 0 | 1 | 4 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0002c0002t0005 | 0/0 | 7817 | 2 | 0 | 0 | 2 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0002c0002t0006 | 0/0 | 7817 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0002c0002t0007 | 0/0 | 7816 | 3 | 0 | 1 | 2 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0002c0002t0017 | 0/0 | 7818 | 2 | 0 | 2 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0002c0002t0023 | 0/0 | 7838 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0002c0002t0030 | 0/0 | 7818 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0002c0002t0031 | 0/0 | 7818 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0002c0002t0070 | 0/0 | 7816 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0002c0003t0009 | 0/0 | 7839 | 2 | 2 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0002c0003t0014 | 0/0 | 7838 | 3 | 2 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0002c0003t0015 | 0/0 | 7837 | 4 | 4 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0002c0003t0019 | 0/0 | 7839 | 2 | 1 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0002c0003t0039 | 0/0 | 7839 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0002c0003t0041 | 0/0 | 7838 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0002c0003t0042 | 0/0 | 7837 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0002c0006t0036 | 0/0 | 7839 | 2 | 2 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0002c0006t0071 | 0/0 | 7838 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0002c0006t0072 | 0/0 | 7838 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0002c0006t0073 | 0/0 | 7838 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0002c0020t0005 | 0/0 | 7817 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0003c0004t0001 | 0/0 | 7808 | 4 | 1 | 2 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0003c0004t0002 | 0/0 | 7809 | 4 | 3 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0003c0004t0005 | 0/0 | 7808 | 3 | 0 | 0 | 3 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0003c0004t0016 | 0/0 | 7808 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0004c0007t0001 | 0/0 | 7814 | 3 | 0 | 2 | 0 | 1 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0004c0007t0002 | 0/0 | 7815 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0004c0007t0008 | 0/0 | 7815 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0005c0011t0004 | 0/0 | 7812 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0005c0011t0009 | 0/0 | 7833 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0005c0011t0019 | 0/0 | 7833 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0006c0026t0001 | 0/0 | 7814 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0007c0025t0032 | 0/0 | 7832 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0008c0023t0038 | 0/0 | 7815 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0009c0022t0002 | 0/0 | 7818 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0010c0015t0005 | 0/0 | 7814 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0011c0017t0003 | 0/0 | 7814 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0012c0018t0002 | 0/0 | 7815 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
a0013c0024t0009 | 0/0 | 7836 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | copy fasta | chr22 | 27743277 | 27806756 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0101 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0227 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0003g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0003g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0003g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0003g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0003g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0003g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0003g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0003g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0003g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0003g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0003g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0003g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0003g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0003g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0003g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0003g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0003g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0003g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0003g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0003g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0003g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0003g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0003g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0003g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0003g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0003g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0003g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0004g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0004g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0004g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0004g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0004g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0004g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0004g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0004g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0004g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0004g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0004g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0004g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0004g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0004g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0004g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0004g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0004g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0004g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0004g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0004g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0005g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0005g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0005g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0005g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0005g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0005g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0005g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0005g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0005g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0005g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0006g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0006g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0006g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0006g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0006g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0006g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0006g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0006g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0006g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0007g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0007g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0007g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0007g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0007g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0007g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0007g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0007g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0008g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0008g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0008g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0008g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0008g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0008g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0008g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0008g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0009g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0010g0308 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0010g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0010g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0010g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0010g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0010g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0011g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0011g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0011g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0011g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0011g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0012g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0012g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0012g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0012g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0012g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0013g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0013g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0013g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0013g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0013g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0016g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0016g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0017g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0017g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0020g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0020g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0021g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0022g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0022g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0022g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0023g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0024g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0025g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0025g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0026g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0026g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0027g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0027g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0028g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0029g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0029g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0030g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0031g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0032g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0033g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0033g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0034g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0034g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0037g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0044g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0045g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0046g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0047g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0050g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0051g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0052g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0053g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0054g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0055g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0056g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0057g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0058g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0059g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0060g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0061g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0062g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0063g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0064g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0065g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0066g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0067g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0068g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0069g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0074g0385 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0075g0384 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0001t0076g0386 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0005t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0005t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0005t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0005t0006g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0005t0009g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0005t0009g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0005t0016g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0005t0028g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0005t0043g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0005t0049g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0008t0018g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0008t0018g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0008t0035g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0008t0035g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0009t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0009t0006g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0009t0021g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0010t0014g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0010t0024g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0010t0040g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0012t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0012t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0012t0020g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0013t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0013t0048g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0014t0018g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0014t0018g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0016t0003g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0019t0004g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0001c0021t0007g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0002t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0002t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0002t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0002t0003g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0002t0003g0366 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0002t0003g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0002t0004g0007 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0002t0004g0367 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0002t0004g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0002t0004g0370 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0002t0005g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0002t0005g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0002t0006g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0002t0007g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0002t0007g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0002t0007g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0002t0017g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0002t0017g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0002t0023g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0002t0030g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0002t0031g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0002t0070g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0003t0009g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0003t0009g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0003t0014g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0003t0014g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0003t0014g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0003t0015g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0003t0015g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0003t0015g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0003t0015g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0003t0019g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0003t0019g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0003t0039g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0003t0041g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0003t0042g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0006t0036g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0006t0071g0382 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0006t0072g0383 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0006t0073g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0002c0020t0005g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0003c0004t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0003c0004t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0003c0004t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0003c0004t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0003c0004t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0003c0004t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0003c0004t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0003c0004t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0003c0004t0005g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0003c0004t0005g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0003c0004t0016g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0004c0007t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0004c0007t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0004c0007t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0004c0007t0002g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0004c0007t0008g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0005c0011t0004g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0005c0011t0009g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0005c0011t0019g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0006c0026t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0007c0025t0032g0372 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0008c0023t0038g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0009c0022t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0010c0015t0005g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0011c0017t0003g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0012c0018t0002g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
a0013c0024t0009g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0051 | g0138 | EUR | GBR | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0099 | EUR | GBR | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG00140 | hp1 | a0001 | c0001 | t0008 | g0056 | EUR | GBR | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0202 | EUR | GBR | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG00280 | hp1 | a0001 | c0001 | t0005 | g0145 | EUR | FIN | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG00280 | hp2 | a0001 | c0001 | t0008 | g0067 | EUR | FIN | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0090 | EUR | FIN | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0066 | EUR | FIN | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG00408 | hp1 | a0001 | c0001 | t0003 | g0282 | EAS | CHS | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | CHS | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG00423 | hp1 | a0001 | c0001 | t0011 | g0142 | EAS | CHS | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG00423 | hp2 | a0001 | c0001 | t0004 | g0353 | EAS | CHS | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | CHS | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG00438 | hp2 | a0002 | c0002 | t0004 | g0368 | EAS | CHS | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | CHS | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG00558 | hp2 | a0001 | c0001 | t0004 | g0321 | EAS | CHS | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | CHS | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG00609 | hp2 | a0001 | c0001 | t0012 | g0354 | EAS | CHS | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG00621 | hp1 | a0002 | c0002 | t0001 | g0259 | EAS | CHS | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG00621 | hp2 | a0003 | c0004 | t0001 | g0245 | EAS | CHS | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG00639 | hp2 | a0001 | c0001 | t0029 | g0060 | AMR | PUR | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG00642 | hp2 | a0002 | c0002 | t0002 | g0263 | AMR | PUR | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG00673 | hp1 | a0001 | c0001 | t0013 | g0330 | EAS | CHS | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0212 | EAS | CHS | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG00733 | hp1 | a0002 | c0002 | t0007 | g0258 | AMR | PUR | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG00733 | hp2 | a0004 | c0007 | t0008 | g0274 | AMR | PUR | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0062 | AMR | PUR | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG00738 | hp1 | a0001 | c0001 | t0027 | g0154 | AMR | PUR | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0075 | AMR | PUR | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG00741 | hp1 | a0001 | c0001 | t0005 | g0165 | AMR | PUR | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG00741 | hp2 | a0003 | c0004 | t0001 | g0239 | AMR | PUR | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01069 | hp1 | a0001 | c0001 | t0029 | g0164 | AMR | PUR | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01069 | hp2 | a0002 | c0002 | t0017 | g0365 | AMR | PUR | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01070 | hp2 | a0001 | c0001 | t0004 | g0358 | AMR | PUR | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01071 | hp2 | a0002 | c0002 | t0017 | g0364 | AMR | PUR | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0068 | AMR | PUR | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01081 | hp2 | a0001 | c0001 | t0031 | g0296 | AMR | PUR | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01099 | hp1 | a0001 | c0001 | t0058 | g0233 | AMR | PUR | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01099 | hp2 | a0001 | c0001 | t0017 | g0352 | AMR | PUR | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0185 | AMR | PUR | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01109 | hp1 | a0001 | c0001 | t0027 | g0102 | AMR | PUR | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0163 | AMR | PUR | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01167 | hp1 | a0003 | c0004 | t0001 | g0241 | AMR | PUR | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01167 | hp2 | a0001 | c0001 | t0030 | g0169 | AMR | PUR | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01175 | hp2 | a0001 | c0001 | t0062 | g0063 | AMR | PUR | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01192 | hp1 | a0003 | c0004 | t0002 | g0242 | AMR | PUR | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0070 | AMR | PUR | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01243 | hp1 | a0001 | c0005 | t0006 | g0049 | AMR | PUR | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01243 | hp2 | a0002 | c0003 | t0014 | g0034 | AMR | PUR | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0201 | AMR | CLM | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01255 | hp2 | a0001 | c0001 | t0017 | g0351 | AMR | CLM | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0088 | AMR | CLM | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01257 | hp1 | a0002 | c0002 | t0001 | g0265 | AMR | CLM | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0087 | AMR | CLM | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0089 | AMR | CLM | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0192 | AMR | CLM | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01261 | hp2 | a0004 | c0007 | t0001 | g0272 | AMR | CLM | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01346 | hp1 | a0001 | c0001 | t0004 | g0335 | AMR | CLM | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | CLM | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01358 | hp1 | a0001 | c0001 | t0005 | g0084 | AMR | CLM | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01358 | hp2 | a0001 | c0001 | t0004 | g0334 | AMR | CLM | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | CLM | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0106 | AMR | CLM | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01433 | hp2 | a0002 | c0002 | t0031 | g0371 | AMR | CLM | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01496 | hp1 | a0001 | c0005 | t0009 | g0016 | AMR | CLM | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01496 | hp2 | a0002 | c0003 | t0019 | g0032 | AMR | CLM | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01515 | hp1 | a0002 | c0002 | t0004 | g0370 | EUR | IBS | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0209 | EUR | IBS | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01516 | hp1 | a0002 | c0002 | t0004 | g0007 | EUR | IBS | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01516 | hp2 | a0004 | c0007 | t0001 | g0273 | EUR | IBS | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01517 | hp1 | a0002 | c0002 | t0004 | g0007 | EUR | IBS | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0210 | EUR | IBS | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01884 | hp1 | a0002 | c0003 | t0015 | g0026 | AFR | ACB | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01884 | hp2 | a0002 | c0003 | t0039 | g0028 | AFR | ACB | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0232 | AFR | ACB | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0223 | AFR | ACB | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01928 | hp1 | a0001 | c0001 | t0005 | g0153 | AMR | PEL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01934 | hp1 | a0001 | c0001 | t0046 | g0038 | AMR | PEL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01934 | hp2 | a0001 | c0001 | t0005 | g0162 | AMR | PEL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0197 | AMR | PEL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01952 | hp2 | a0001 | c0001 | t0020 | g0143 | AMR | PEL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01975 | hp1 | a0001 | c0001 | t0005 | g0077 | AMR | PEL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | PEL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01978 | hp1 | a0002 | c0002 | t0001 | g0262 | AMR | PEL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01978 | hp2 | a0001 | c0001 | t0003 | g0297 | AMR | PEL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0225 | AMR | PEL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02004 | hp1 | a0001 | c0001 | t0004 | g0293 | AMR | PEL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0105 | AMR | PEL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02015 | hp1 | a0001 | c0001 | t0013 | g0343 | EAS | KHV | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02015 | hp2 | a0001 | c0001 | t0004 | g0281 | EAS | KHV | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02027 | hp1 | a0001 | c0001 | t0003 | g0355 | EAS | KHV | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02027 | hp2 | a0002 | c0020 | t0005 | g0249 | EAS | KHV | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02040 | hp1 | a0001 | c0001 | t0004 | g0310 | EAS | KHV | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | KHV | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02055 | hp1 | a0003 | c0004 | t0001 | g0247 | AFR | ACB | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02055 | hp2 | a0001 | c0001 | t0069 | g0373 | AFR | ACB | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | KHV | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02056 | hp2 | a0001 | c0001 | t0003 | g0309 | EAS | KHV | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02071 | hp1 | a0001 | c0001 | t0012 | g0311 | EAS | KHV | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | KHV | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02074 | hp1 | a0002 | c0002 | t0005 | g0253 | EAS | KHV | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02074 | hp2 | a0002 | c0002 | t0007 | g0261 | EAS | KHV | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02080 | hp1 | a0001 | c0001 | t0013 | g0299 | EAS | KHV | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02080 | hp2 | a0001 | c0001 | t0026 | g0043 | EAS | KHV | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02083 | hp1 | a0001 | c0001 | t0004 | g0349 | EAS | KHV | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02083 | hp2 | a0001 | c0001 | t0003 | g0301 | EAS | KHV | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02132 | hp1 | a0001 | c0001 | t0003 | g0339 | EAS | KHV | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02132 | hp2 | a0001 | c0001 | t0010 | g0322 | EAS | KHV | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02135 | hp1 | a0001 | c0001 | t0003 | g0348 | EAS | KHV | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02135 | hp2 | a0002 | c0002 | t0003 | g0369 | EAS | KHV | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02145 | hp1 | a0001 | c0001 | t0009 | g0020 | AFR | ACB | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02145 | hp2 | a0002 | c0003 | t0042 | g0030 | AFR | ACB | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PEL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02148 | hp2 | a0002 | c0002 | t0003 | g0363 | AMR | PEL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | CDX | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | CDX | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02257 | hp1 | a0001 | c0014 | t0018 | g0374 | AFR | ACB | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02257 | hp2 | a0002 | c0003 | t0015 | g0024 | AFR | ACB | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02258 | hp2 | a0001 | c0009 | t0006 | g0268 | AFR | ACB | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0184 | AMR | PEL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02280 | hp1 | a0001 | c0005 | t0002 | g0054 | AFR | ACB | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02280 | hp2 | a0003 | c0004 | t0002 | g0246 | AFR | ACB | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0182 | AMR | PEL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02293 | hp2 | a0001 | c0001 | t0008 | g0092 | AMR | PEL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | PEL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PEL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02451 | hp1 | a0001 | c0005 | t0049 | g0052 | AFR | ACB | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02451 | hp2 | a0003 | c0004 | t0016 | g0248 | AFR | ACB | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02523 | hp1 | a0001 | c0001 | t0004 | g0347 | EAS | KHV | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02523 | hp2 | a0001 | c0001 | t0003 | g0341 | EAS | KHV | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02572 | hp1 | a0002 | c0003 | t0015 | g0025 | AFR | GWD | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02572 | hp2 | a0001 | c0001 | t0074 | g0385 | AFR | GWD | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02602 | hp1 | a0001 | c0001 | t0032 | g0360 | SAS | PJL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0095 | SAS | PJL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02622 | hp1 | a0001 | c0010 | t0024 | g0013 | AFR | GWD | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02622 | hp2 | a0001 | c0001 | t0016 | g0224 | AFR | GWD | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02630 | hp1 | a0001 | c0001 | t0061 | g0222 | AFR | GWD | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0175 | AFR | GWD | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0236 | AFR | GWD | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02647 | hp2 | a0001 | c0001 | t0021 | g0073 | AFR | GWD | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02683 | hp1 | a0001 | c0001 | t0008 | g0096 | SAS | PJL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0108 | SAS | PJL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02698 | hp1 | a0010 | c0015 | t0005 | g0045 | SAS | PJL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02717 | hp1 | a0002 | c0003 | t0014 | g0029 | AFR | GWD | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02717 | hp2 | a0001 | c0001 | t0059 | g0231 | AFR | GWD | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02735 | hp1 | a0001 | c0001 | t0008 | g0228 | SAS | PJL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0194 | SAS | PJL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02738 | hp1 | a0001 | c0001 | t0025 | g0039 | SAS | PJL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02738 | hp2 | a0002 | c0002 | t0003 | g0366 | SAS | PJL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02809 | hp1 | a0002 | c0006 | t0071 | g0382 | AFR | GWD | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02809 | hp2 | a0001 | c0001 | t0044 | g0040 | AFR | GWD | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02818 | hp1 | a0002 | c0003 | t0041 | g0027 | AFR | GWD | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02818 | hp2 | a0001 | c0001 | t0033 | g0318 | AFR | GWD | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02886 | hp1 | a0002 | c0006 | t0036 | g0008 | AFR | GWD | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02886 | hp2 | a0001 | c0001 | t0025 | g0041 | AFR | GWD | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02895 | hp1 | a0001 | c0009 | t0021 | g0006 | AFR | GWD | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02895 | hp2 | a0001 | c0001 | t0006 | g0218 | AFR | GWD | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02896 | hp1 | a0001 | c0008 | t0035 | g0377 | AFR | GWD | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02896 | hp2 | a0001 | c0013 | t0001 | g0047 | AFR | GWD | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02897 | hp1 | a0001 | c0009 | t0021 | g0006 | AFR | GWD | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02897 | hp2 | a0001 | c0008 | t0035 | g0378 | AFR | GWD | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02922 | hp1 | a0001 | c0005 | t0002 | g0048 | AFR | ESN | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0125 | AFR | ESN | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02970 | hp1 | a0001 | c0010 | t0014 | g0011 | AFR | ESN | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02970 | hp2 | a0001 | c0005 | t0002 | g0050 | AFR | ESN | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0057 | AFR | ESN | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02976 | hp2 | a0002 | c0003 | t0015 | g0023 | AFR | ESN | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03041 | hp1 | a0002 | c0006 | t0036 | g0008 | AFR | GWD | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03041 | hp2 | a0001 | c0001 | t0075 | g0384 | AFR | GWD | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03098 | hp1 | a0003 | c0004 | t0002 | g0243 | AFR | MSL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03098 | hp2 | a0001 | c0001 | t0023 | g0019 | AFR | MSL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03130 | hp1 | a0001 | c0008 | t0018 | g0376 | AFR | ESN | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03130 | hp2 | a0002 | c0002 | t0023 | g0035 | AFR | ESN | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03139 | hp1 | a0001 | c0010 | t0040 | g0012 | AFR | ESN | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03139 | hp2 | a0001 | c0005 | t0028 | g0051 | AFR | ESN | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03195 | hp1 | a0001 | c0001 | t0002 | g0116 | AFR | ESN | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03195 | hp2 | a0001 | c0001 | t0060 | g0171 | AFR | ESN | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03209 | hp1 | a0001 | c0009 | t0002 | g0269 | AFR | MSL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03209 | hp2 | a0001 | c0001 | t0016 | g0110 | AFR | MSL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03225 | hp1 | a0005 | c0011 | t0009 | g0014 | AFR | MSL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03225 | hp2 | a0001 | c0001 | t0057 | g0237 | AFR | MSL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03239 | hp1 | a0001 | c0001 | t0003 | g0326 | SAS | PJL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03453 | hp1 | a0001 | c0014 | t0018 | g0375 | AFR | MSL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03453 | hp2 | a0001 | c0001 | t0076 | g0386 | AFR | MSL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03486 | hp1 | a0001 | c0001 | t0002 | g0206 | AFR | MSL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03486 | hp2 | a0001 | c0005 | t0016 | g0053 | AFR | MSL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03516 | hp1 | a0001 | c0013 | t0048 | g0046 | AFR | ESN | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0230 | AFR | ESN | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0214 | AFR | GWD | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0213 | AFR | GWD | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03579 | hp1 | a0001 | c0005 | t0009 | g0017 | AFR | MSL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03579 | hp2 | a0001 | c0001 | t0028 | g0234 | AFR | MSL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03654 | hp2 | a0012 | c0018 | t0002 | g0238 | SAS | PJL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03669 | hp1 | a0004 | c0007 | t0002 | g0271 | SAS | PJL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0172 | SAS | PJL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | PJL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0114 | SAS | PJL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03710 | hp2 | a0005 | c0011 | t0004 | g0279 | SAS | PJL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03831 | hp1 | a0002 | c0002 | t0006 | g0266 | SAS | BEB | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03831 | hp2 | a0001 | c0001 | t0055 | g0198 | SAS | BEB | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | BEB | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0055 | SAS | BEB | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | BEB | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03927 | hp2 | a0001 | c0001 | t0003 | g0319 | SAS | BEB | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG04115 | hp1 | a0007 | c0025 | t0032 | g0372 | SAS | STU | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG04115 | hp2 | a0001 | c0001 | t0008 | g0199 | SAS | STU | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0179 | SAS | BEB | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG04184 | hp2 | a0001 | c0001 | t0037 | g0009 | SAS | BEB | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG04199 | hp1 | a0001 | c0001 | t0024 | g0018 | SAS | STU | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG04199 | hp2 | a0001 | c0001 | t0004 | g0357 | SAS | STU | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | STU | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0167 | SAS | STU | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | STU | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | STU | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18522 | hp1 | a0002 | c0003 | t0019 | g0033 | AFR | YRI | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18522 | hp2 | a0005 | c0011 | t0019 | g0015 | AFR | YRI | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18612 | hp1 | a0001 | c0001 | t0007 | g0173 | EAS | CHB | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18612 | hp2 | a0001 | c0012 | t0001 | g0277 | EAS | CHB | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18747 | hp1 | a0001 | c0001 | t0022 | g0292 | EAS | CHB | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18747 | hp2 | a0001 | c0001 | t0005 | g0109 | EAS | CHB | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18906 | hp1 | a0001 | c0021 | t0007 | g0250 | AFR | YRI | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18906 | hp2 | a0002 | c0006 | t0073 | g0381 | AFR | YRI | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18940 | hp1 | a0001 | c0001 | t0004 | g0312 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18940 | hp2 | a0001 | c0001 | t0054 | g0150 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18941 | hp1 | a0001 | c0012 | t0020 | g0276 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18941 | hp2 | a0001 | c0001 | t0007 | g0091 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18942 | hp1 | a0001 | c0001 | t0010 | g0325 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18942 | hp2 | a0003 | c0004 | t0005 | g0244 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18944 | hp1 | a0001 | c0001 | t0022 | g0305 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18944 | hp2 | a0001 | c0001 | t0006 | g0216 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18945 | hp1 | a0001 | c0001 | t0003 | g0359 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18945 | hp2 | a0002 | c0002 | t0007 | g0256 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18947 | hp1 | a0001 | c0001 | t0003 | g0329 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18947 | hp2 | a0001 | c0001 | t0004 | g0285 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18950 | hp1 | a0001 | c0001 | t0012 | g0337 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18950 | hp2 | a0001 | c0001 | t0007 | g0189 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18951 | hp1 | a0001 | c0001 | t0034 | g0327 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18951 | hp2 | a0001 | c0001 | t0006 | g0135 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18959 | hp1 | a0001 | c0001 | t0004 | g0356 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18960 | hp1 | a0001 | c0001 | t0005 | g0085 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18960 | hp2 | a0001 | c0001 | t0056 | g0127 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18962 | hp2 | a0001 | c0001 | t0034 | g0286 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18964 | hp2 | a0001 | c0001 | t0004 | g0346 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18965 | hp1 | a0008 | c0023 | t0038 | g0010 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18965 | hp2 | a0001 | c0001 | t0003 | g0290 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18966 | hp1 | a0001 | c0001 | t0006 | g0129 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18966 | hp2 | a0001 | c0001 | t0020 | g0160 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18967 | hp1 | a0001 | c0001 | t0010 | g0323 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18967 | hp2 | a0002 | c0002 | t0002 | g0257 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18968 | hp1 | a0001 | c0001 | t0010 | g0328 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18969 | hp1 | a0001 | c0001 | t0067 | g0283 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18969 | hp2 | a0001 | c0019 | t0004 | g0362 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18970 | hp1 | a0001 | c0001 | t0006 | g0215 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18971 | hp1 | a0001 | c0001 | t0065 | g0294 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18971 | hp2 | a0002 | c0002 | t0001 | g0254 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18974 | hp1 | a0009 | c0022 | t0002 | g0251 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18974 | hp2 | a0001 | c0001 | t0007 | g0115 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18979 | hp1 | a0001 | c0001 | t0004 | g0289 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18979 | hp2 | a0001 | c0001 | t0050 | g0174 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18980 | hp1 | a0001 | c0016 | t0003 | g0280 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18980 | hp2 | a0001 | c0001 | t0011 | g0069 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18981 | hp1 | a0001 | c0001 | t0003 | g0316 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18983 | hp2 | a0001 | c0001 | t0006 | g0159 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18984 | hp1 | a0001 | c0001 | t0013 | g0345 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18984 | hp2 | a0001 | c0001 | t0003 | g0350 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18992 | hp1 | a0001 | c0001 | t0026 | g0044 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18993 | hp2 | a0001 | c0001 | t0012 | g0298 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18994 | hp1 | a0002 | c0002 | t0001 | g0252 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18994 | hp2 | a0001 | c0001 | t0003 | g0332 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18995 | hp1 | a0001 | c0001 | t0012 | g0304 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18998 | hp1 | a0001 | c0001 | t0007 | g0161 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18998 | hp2 | a0001 | c0001 | t0003 | g0320 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18999 | hp1 | a0001 | c0001 | t0003 | g0342 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19000 | hp1 | a0002 | c0002 | t0001 | g0264 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19000 | hp2 | a0001 | c0001 | t0006 | g0103 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19004 | hp1 | a0001 | c0001 | t0066 | g0307 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19004 | hp2 | a0001 | c0001 | t0003 | g0300 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19005 | hp1 | a0001 | c0001 | t0047 | g0181 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19005 | hp2 | a0002 | c0002 | t0030 | g0260 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19007 | hp1 | a0002 | c0002 | t0005 | g0267 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19007 | hp2 | a0001 | c0001 | t0003 | g0315 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19009 | hp1 | a0001 | c0001 | t0004 | g0314 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19009 | hp2 | a0003 | c0004 | t0005 | g0005 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19010 | hp1 | a0001 | c0001 | t0011 | g0104 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19010 | hp2 | a0001 | c0001 | t0010 | g0324 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19030 | hp1 | a0002 | c0003 | t0014 | g0021 | AFR | LWK | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | LWK | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19043 | hp1 | a0001 | c0001 | t0053 | g0123 | AFR | LWK | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19043 | hp2 | a0001 | c0001 | t0002 | g0126 | AFR | LWK | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19056 | hp1 | a0001 | c0001 | t0006 | g0186 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19056 | hp2 | a0001 | c0001 | t0011 | g0120 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19060 | hp2 | a0002 | c0002 | t0070 | g0380 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19063 | hp1 | a0001 | c0001 | t0003 | g0306 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19063 | hp2 | a0001 | c0001 | t0007 | g0118 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19064 | hp1 | a0001 | c0001 | t0052 | g0080 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19064 | hp2 | a0001 | c0001 | t0004 | g0336 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19065 | hp1 | a0011 | c0017 | t0003 | g0361 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19065 | hp2 | a0003 | c0004 | t0005 | g0005 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19066 | hp1 | a0001 | c0001 | t0005 | g0170 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19066 | hp2 | a0001 | c0001 | t0003 | g0291 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19070 | hp2 | a0001 | c0001 | t0063 | g0284 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19077 | hp1 | a0002 | c0002 | t0002 | g0255 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19077 | hp2 | a0001 | c0001 | t0013 | g0344 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19078 | hp1 | a0001 | c0001 | t0005 | g0122 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19078 | hp2 | a0001 | c0001 | t0004 | g0295 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19079 | hp2 | a0001 | c0001 | t0003 | g0313 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19081 | hp1 | a0001 | c0001 | t0004 | g0317 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19081 | hp2 | a0001 | c0001 | t0003 | g0340 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19087 | hp1 | a0001 | c0012 | t0001 | g0278 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19087 | hp2 | a0001 | c0001 | t0022 | g0333 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19088 | hp1 | a0001 | c0001 | t0003 | g0288 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19088 | hp2 | a0001 | c0001 | t0064 | g0302 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19089 | hp2 | a0001 | c0001 | t0006 | g0133 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19090 | hp1 | a0001 | c0001 | t0007 | g0121 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19090 | hp2 | a0001 | c0001 | t0011 | g0168 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19091 | hp2 | a0001 | c0001 | t0003 | g0303 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19240 | hp1 | a0002 | c0003 | t0009 | g0031 | AFR | YRI | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | YRI | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA20129 | hp1 | a0001 | c0001 | t0045 | g0042 | AFR | ASW | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | ASW | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA20752 | hp1 | a0002 | c0002 | t0004 | g0367 | EUR | TSI | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA20752 | hp2 | a0001 | c0001 | t0010 | g0308 | EUR | TSI | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA20805 | hp1 | a0001 | c0001 | t0008 | g0200 | EUR | TSI | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0059 | EUR | TSI | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA20905 | hp1 | a0001 | c0001 | t0008 | g0196 | SAS | GIH | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA20905 | hp2 | a0006 | c0026 | t0001 | g0275 | SAS | GIH | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | CLM | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG01123 | hp2 | a0004 | c0007 | t0001 | g0270 | AMR | CLM | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02109 | hp1 | a0001 | c0001 | t0033 | g0287 | AFR | ACB | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02109 | hp2 | a0002 | c0006 | t0072 | g0383 | AFR | ACB | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02486 | hp1 | a0001 | c0001 | t0007 | g0112 | AFR | ACB | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0176 | AFR | ACB | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02559 | hp1 | a0001 | c0008 | t0018 | g0379 | AFR | ACB | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG02559 | hp2 | a0001 | c0001 | t0068 | g0331 | AFR | ACB | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0058 | AFR | MSL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG03471 | hp2 | a0003 | c0004 | t0002 | g0240 | AFR | MSL | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG06807 | hp1 | a0013 | c0024 | t0009 | g0036 | AFR | USA | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
HG06807 | hp2 | a0002 | c0003 | t0009 | g0022 | AFR | USA | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18955 | hp1 | a0001 | c0001 | t0003 | g0338 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | USA | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0190 | AFR | USA | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA21309 | hp1 | a0001 | c0005 | t0043 | g0037 | AFR | LWK | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | LWK | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0227 | REF | REF | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0101 | REF | REF | MN1_chr22_27743277_27806756 | MN1 | chr22 | 27743277 | 27806756 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:27797603
|
C | A | 1 | a0011 | 1 | NA19065.hp1 | missense_variant | MODERATE | c.2941G>T | p.Ala981Ser | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | 4154/7814 | 2941/3963 | 981/1320 | chr22 | 27797603 | ||
chr22:27798238
|
G | C | 1 | a0012 | 1 | HG03654.hp2 | missense_variant | MODERATE | c.2306C>G | p.Ala769Gly | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | 3519/7814 | 2306/3963 | 769/1320 | chr22 | 27798238 | ||
chr22:27798761
|
C | T | 2 | a0009a0010 | 2 | HG02698.hp1 NA18974.hp1 |
missense_variant | MODERATE | c.1783G>A | p.Val595Met | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | 2996/7814 | 1783/3963 | 595/1320 | chr22 | 27798761 | ||
chr22:27798906
|
CTGCTGT | C | 1 | a0003 | 12 | HG00621.hp2 HG00741.hp2 HG01167.hp1 others(9): Show |
disruptive_inframe_deletion | MODERATE | c.1632_1637delACAGCA | p.Gln545_Gln546del | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | 2850/7814 | 1632/3963 | 544/1320 | chr22 | 27798906 | ||
chr22:27798924
|
T | TTGC | 1 | a0002 | 15 | HG01243.hp2 HG01496.hp2 HG01884.hp1 others(12): Show |
disruptive_inframe_insertion | MODERATE | c.1617_1619dupGCA | p.Gln540dup | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | 2832/7814 | 1619/3963 | 540/1320 | chr22 | 27798924 | ||
chr22:27798945
|
T | TTGC | 2 | a0002a0009 | 35 | HG00438.hp2 HG00621.hp1 HG00642.hp2 others(32): Show |
disruptive_inframe_insertion | MODERATE | c.1596_1598dupGCA | p.Gln533dup | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | 2811/7814 | 1598/3963 | 533/1320 | chr22 | 27798945 | ||
chr22:27798945
|
TTGC | T | 1 | a0005 | 3 | HG03225.hp1 HG03710.hp2 NA18522.hp2 |
disruptive_inframe_deletion | MODERATE | c.1596_1598delGCA | p.Gln533del | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | 2811/7814 | 1596/3963 | 532/1320 | chr22 | 27798945 | ||
chr22:27799021
|
G | A | 1 | a0008 | 1 | NA18965.hp1 | missense_variant | MODERATE | c.1523C>T | p.Ser508Leu | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | 2736/7814 | 1523/3963 | 508/1320 | chr22 | 27799021 | ||
chr22:27799043
|
G | A | 1 | a0013 | 1 | HG06807.hp1 | missense_variant | MODERATE | c.1501C>T | p.Pro501Ser | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | 2714/7814 | 1501/3963 | 501/1320 | chr22 | 27799043 | ||
chr22:27799398
|
C | A | 1 | a0004 | 5 | HG00733.hp2 HG01123.hp2 HG01261.hp2 others(2): Show |
missense_variant | MODERATE | c.1146G>T | p.Gln382His | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | 2359/7814 | 1146/3963 | 382/1320 | chr22 | 27799398 | ||
chr22:27799618
|
T | TGCTGCTG others(11): Show |
1 | a0007 | 1 | HG04115.hp1 | conservative_inframe_insertion | MODERATE | c.908_925dupCCCAGCAG others(10): Show |
p.Pro303_Gln308dup | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | 2138/7814 | 925/3963 | 309/1320 | chr22 | 27799618 | ||
chr22:27800048
|
C | A | 1 | a0006 | 1 | NA20905.hp2 | missense_variant | MODERATE | c.496G>T | p.Gly166Cys | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | 1709/7814 | 496/3963 | 166/1320 | chr22 | 27800048 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:27797109
|
C | T | 3 | a0001c0010a0001c0013a0002c0003 | 19 | HG01243.hp2 HG01496.hp2 HG01884.hp1 others(16): Show |
synonymous_variant | LOW | c.3435G>A | p.Pro1145Pro | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | 4648/7814 | 3435/3963 | 1145/1320 | chr22 | 27797109 | ||
chr22:27797610
|
C | T | 1 | a0001c0016 | 1 | NA18980.hp1 | synonymous_variant | LOW | c.2934G>A | p.Gln978Gln | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | 4147/7814 | 2934/3963 | 978/1320 | chr22 | 27797610 | ||
chr22:27798072
|
G | A | 1 | a0001c0014 | 2 | HG02257.hp1 HG03453.hp1 |
synonymous_variant | LOW | c.2472C>T | p.Cys824Cys | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | 3685/7814 | 2472/3963 | 824/1320 | chr22 | 27798072 | ||
chr22:27798465
|
G | A | 1 | a0001c0019 | 1 | NA18969.hp2 | synonymous_variant | LOW | c.2079C>T | p.Pro693Pro | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | 3292/7814 | 2079/3963 | 693/1320 | chr22 | 27798465 | ||
chr22:27798759
|
C | T | 5 | a0001c0005a0001c0010a0001c0013others(2): Show | 34 | HG01243.hp1 HG01243.hp2 HG01496.hp1 others(31): Show |
synonymous_variant | LOW | c.1785G>A | p.Val595Val | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | 2998/7814 | 1785/3963 | 595/1320 | chr22 | 27798759 | ||
chr22:27798924
|
T | C | 1 | a0001c0021 | 1 | NA18906.hp1 | synonymous_variant | LOW | c.1620A>G | p.Gln540Gln | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | 2833/7814 | 1620/3963 | 540/1320 | chr22 | 27798924 | ||
chr22:27798945
|
T | C | 1 | a0001c0008 | 4 | HG02559.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
synonymous_variant | LOW | c.1599A>G | p.Gln533Gln | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | 2812/7814 | 1599/3963 | 533/1320 | chr22 | 27798945 | ||
chr22:27798981
|
G | A | 1 | a0001c0009 | 4 | HG02258.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
synonymous_variant | LOW | c.1563C>T | p.Ser521Ser | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | 2776/7814 | 1563/3963 | 521/1320 | chr22 | 27798981 | ||
chr22:27799020
|
C | G | 1 | a0008c0023 | 1 | NA18965.hp1 | synonymous_variant | LOW | c.1524G>C | p.Ser508Ser | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | 2737/7814 | 1524/3963 | 508/1320 | chr22 | 27799020 | ||
chr22:27799989
|
G | T | 1 | a0002c0006 | 5 | HG02109.hp2 HG02809.hp1 HG02886.hp1 others(2): Show |
synonymous_variant | LOW | c.555C>A | p.Ala185Ala | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | 1768/7814 | 555/3963 | 185/1320 | chr22 | 27799989 | ||
chr22:27800136
|
G | A | 1 | a0001c0012 | 3 | NA18612.hp2 NA18941.hp1 NA19087.hp1 |
synonymous_variant | LOW | c.408C>T | p.Tyr136Tyr | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | 1621/7814 | 408/3963 | 136/1320 | chr22 | 27800136 | ||
chr22:27800238
|
C | G | 1 | a0001c0010 | 3 | HG02622.hp1 HG02970.hp1 HG03139.hp1 |
synonymous_variant | LOW | c.306G>C | p.Pro102Pro | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | 1519/7814 | 306/3963 | 102/1320 | chr22 | 27800238 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:27748391
|
GA | G | 22 | a0001c0001t0006a0001c0001t0007a0001c0001t0010others(19): Show | 49 | HG00609.hp2 HG00733.hp1 HG01243.hp1 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*2523delT | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 2523 | chr22 | 27748391 | |||||
chr22:27748469
|
A | G | 1 | a0001c0001t0037 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2446T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 2446 | chr22 | 27748469 | |||||
chr22:27748636
|
T | G | 11 | a0001c0001t0005a0001c0001t0020a0001c0001t0022others(8): Show | 26 | HG00280.hp1 HG00741.hp1 HG01358.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*2279A>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 2279 | chr22 | 27748636 | |||||
chr22:27748777
|
G | T | 1 | a0001c0001t0050 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2138C>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 2138 | chr22 | 27748777 | |||||
chr22:27748879
|
A | G | 1 | a0001c0001t0064 | 1 | NA19088.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2036T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 2036 | chr22 | 27748879 | |||||
chr22:27748897
|
C | T | 1 | a0002c0006t0072 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2018G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 2018 | chr22 | 27748897 | |||||
chr22:27749000
|
C | T | 2 | a0001c0001t0068a0002c0006t0071 | 2 | HG02559.hp2 HG02809.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1915G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 1915 | chr22 | 27749000 | |||||
chr22:27749093
|
C | T | 1 | a0001c0001t0056 | 1 | NA18960.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1822G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 1822 | chr22 | 27749093 | |||||
chr22:27749156
|
G | T | 1 | a0001c0001t0055 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1759C>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 1759 | chr22 | 27749156 | |||||
chr22:27749160
|
G | A | 10 | a0001c0001t0005a0001c0001t0020a0001c0001t0022others(7): Show | 25 | HG00280.hp1 HG00741.hp1 HG01358.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1755C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 1755 | chr22 | 27749160 | |||||
chr22:27749226
|
G | A | 10 | a0001c0001t0017a0001c0001t0044a0001c0001t0051others(7): Show | 16 | HG00099.hp1 HG01069.hp2 HG01071.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1689C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 1689 | chr22 | 27749226 | |||||
chr22:27749265
|
T | C | 1 | a0001c0001t0057 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1650A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 1650 | chr22 | 27749265 | |||||
chr22:27749339
|
G | A | 1 | a0001c0001t0029 | 2 | HG00639.hp2 HG01069.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1576C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 1576 | chr22 | 27749339 | |||||
chr22:27749517
|
G | A | 4 | a0001c0001t0011a0001c0001t0013a0001c0001t0052others(1): Show | 12 | HG00423.hp1 HG00673.hp1 HG02015.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1398C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 1398 | chr22 | 27749517 | |||||
chr22:27749545
|
A | T | 1 | a0001c0001t0054 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1370T>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 1370 | chr22 | 27749545 | |||||
chr22:27749546
|
A | G | 2 | a0001c0001t0028a0001c0005t0028 | 2 | HG03139.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1369T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 1369 | chr22 | 27749546 | |||||
chr22:27749547
|
C | T | 1 | a0001c0001t0054 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1368G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 1368 | chr22 | 27749547 | |||||
chr22:27749548
|
C | A | 1 | a0001c0001t0054 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1367G>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 1367 | chr22 | 27749548 | |||||
chr22:27749549
|
A | C | 1 | a0001c0001t0054 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1366T>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 1366 | chr22 | 27749549 | |||||
chr22:27749550
|
C | A | 1 | a0001c0001t0054 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1365G>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 1365 | chr22 | 27749550 | |||||
chr22:27749551
|
C | T | 1 | a0001c0001t0054 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1364G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 1364 | chr22 | 27749551 | |||||
chr22:27749553
|
C | G | 1 | a0001c0001t0054 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1362G>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 1362 | chr22 | 27749553 | |||||
chr22:27749555
|
C | G | 1 | a0001c0001t0054 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1360G>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 1360 | chr22 | 27749555 | |||||
chr22:27749558
|
C | G | 1 | a0001c0001t0054 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1357G>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 1357 | chr22 | 27749558 | |||||
chr22:27749560
|
C | T | 1 | a0001c0001t0054 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1355G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 1355 | chr22 | 27749560 | |||||
chr22:27749617
|
C | T | 9 | a0001c0001t0008a0001c0001t0027a0001c0001t0031others(6): Show | 17 | HG00140.hp1 HG00280.hp2 HG00733.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1298G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 1298 | chr22 | 27749617 | |||||
chr22:27749618
|
A | C | 1 | a0001c0010t0040 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1297T>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 1297 | chr22 | 27749618 | |||||
chr22:27749683
|
C | T | 2 | a0001c0001t0021a0001c0009t0021 | 3 | HG02647.hp2 HG02895.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1232G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 1232 | chr22 | 27749683 | |||||
chr22:27749937
|
C | T | 6 | a0001c0001t0044a0001c0001t0074a0001c0005t0049others(3): Show | 10 | HG01884.hp1 HG02257.hp2 HG02451.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*978G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 978 | chr22 | 27749937 | |||||
chr22:27750065
|
G | A | 1 | a0001c0001t0052 | 1 | NA19064.hp1 | 3_prime_UTR_variant | MODIFIER | c.*850C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 850 | chr22 | 27750065 | |||||
chr22:27750141
|
T | A | 2 | a0001c0001t0058a0001c0001t0069 | 2 | HG01099.hp1 HG02055.hp2 |
3_prime_UTR_variant | MODIFIER | c.*774A>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 774 | chr22 | 27750141 | |||||
chr22:27750147
|
C | T | 1 | a0002c0003t0039 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*768G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 768 | chr22 | 27750147 | |||||
chr22:27750225
|
A | G | 1 | a0001c0001t0054 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*690T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 690 | chr22 | 27750225 | |||||
chr22:27750288
|
CG | C | 6 | a0001c0001t0044a0001c0001t0053a0001c0001t0074others(3): Show | 10 | HG01884.hp1 HG02257.hp2 HG02572.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*626delC | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 626 | chr22 | 27750288 | |||||
chr22:27750289
|
G | A | 1 | a0001c0001t0046 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*626C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 626 | chr22 | 27750289 | |||||
chr22:27750403
|
T | C | 1 | a0002c0003t0041 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*512A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 512 | chr22 | 27750403 | |||||
chr22:27750424
|
T | C | 1 | a0001c0001t0059 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*491A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 491 | chr22 | 27750424 | |||||
chr22:27750747
|
G | A | 6 | a0001c0001t0011a0001c0001t0013a0001c0001t0030others(3): Show | 15 | HG00423.hp1 HG00673.hp1 HG01167.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*168C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 168 | chr22 | 27750747 | |||||
chr22:27750780
|
A | AG | 50 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(47): Show | 166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
3_prime_UTR_variant | MODIFIER | c.*134dupC | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 134 | chr22 | 27750780 | |||||
chr22:27750781
|
G | GA | 6 | a0001c0001t0011a0001c0001t0013a0001c0001t0030others(3): Show | 15 | HG00423.hp1 HG00673.hp1 HG01167.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*133dupT | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 133 | chr22 | 27750781 | |||||
chr22:27750781
|
G | GGA | 8 | a0001c0001t0021a0001c0001t0033a0001c0001t0060others(5): Show | 11 | HG01496.hp2 HG02109.hp1 HG02630.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*133_*134insTC | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 133 | chr22 | 27750781 | |||||
chr22:27750782
|
A | G | 11 | a0001c0001t0016a0001c0001t0044a0001c0001t0074others(8): Show | 18 | HG01243.hp2 HG01884.hp1 HG02257.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*133T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 133 | chr22 | 27750782 | |||||
chr22:27750794
|
C | T | 2 | a0001c0001t0047a0001c0001t0063 | 2 | NA19005.hp1 NA19070.hp2 |
3_prime_UTR_variant | MODIFIER | c.*121G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 2/2 | 121 | chr22 | 27750794 | |||||
chr22:27800547
|
T | G | 1 | a0008c0023t0038 | 1 | NA18965.hp1 | 5_prime_UTR_variant | MODIFIER | c.-4A>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | 4 | chr22 | 27800547 | |||||
chr22:27800736
|
C | G | 1 | a0001c0001t0026 | 2 | HG02080.hp2 NA18992.hp1 |
5_prime_UTR_variant | MODIFIER | c.-193G>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | 193 | chr22 | 27800736 | |||||
chr22:27800752
|
A | G | 1 | a0008c0023t0038 | 1 | NA18965.hp1 | 5_prime_UTR_variant | MODIFIER | c.-209T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | 209 | chr22 | 27800752 | |||||
chr22:27800922
|
G | A | 28 | a0001c0001t0003a0001c0001t0004a0001c0001t0010others(25): Show | 98 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(95): Show |
5_prime_UTR_variant | MODIFIER | c.-379C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | 379 | chr22 | 27800922 | |||||
chr22:27801015
|
T | C | 1 | a0001c0005t0043 | 1 | NA21309.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-472A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | chr22 | 27801015 | ||||||
chr22:27801027
|
A | G | 1 | a0008c0023t0038 | 1 | NA18965.hp1 | 5_prime_UTR_variant | MODIFIER | c.-484T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | 484 | chr22 | 27801027 | |||||
chr22:27801138
|
G | A | 4 | a0001c0001t0025a0001c0001t0044a0001c0001t0045others(1): Show | 5 | HG01934.hp1 HG02738.hp1 HG02809.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-595C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | 595 | chr22 | 27801138 | |||||
chr22:27801274
|
CG | C | 4 | a0001c0001t0069a0001c0008t0018a0001c0008t0035others(1): Show | 7 | HG02055.hp2 HG02257.hp1 HG02559.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-732delC | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | 732 | chr22 | 27801274 | |||||
chr22:27801317
|
C | CTCGGCAG others(14): Show |
27 | a0001c0001t0009a0001c0001t0023a0001c0001t0024others(24): Show | 37 | HG01243.hp2 HG01496.hp1 HG01496.hp2 others(34): Show |
5_prime_UTR_variant | MODIFIER | c.-795_-775dupACGCAG others(15): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | 775 | chr22 | 27801317 | |||||
chr22:27801318
|
T | C | 1 | a0002c0002t0070 | 1 | NA19060.hp2 | 5_prime_UTR_variant | MODIFIER | c.-775A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | 775 | chr22 | 27801318 | |||||
chr22:27801399
|
G | C | 1 | a0008c0023t0038 | 1 | NA18965.hp1 | 5_prime_UTR_variant | MODIFIER | c.-856C>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | 856 | chr22 | 27801399 | |||||
chr22:27801401
|
C | G | 1 | a0008c0023t0038 | 1 | NA18965.hp1 | 5_prime_UTR_variant | MODIFIER | c.-858G>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | 858 | chr22 | 27801401 | |||||
chr22:27801424
|
C | A | 4 | a0002c0006t0036a0002c0006t0071a0002c0006t0072others(1): Show | 5 | HG02109.hp2 HG02809.hp1 HG02886.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-881G>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | 881 | chr22 | 27801424 | |||||
chr22:27801529
|
G | A | 1 | a0008c0023t0038 | 1 | NA18965.hp1 | 5_prime_UTR_variant | MODIFIER | c.-986C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | 986 | chr22 | 27801529 | |||||
chr22:27801530
|
A | T | 1 | a0008c0023t0038 | 1 | NA18965.hp1 | 5_prime_UTR_variant | MODIFIER | c.-987T>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | 987 | chr22 | 27801530 | |||||
chr22:27801613
|
G | C | 3 | a0001c0001t0074a0001c0001t0075a0001c0001t0076 | 3 | HG02572.hp2 HG03041.hp2 HG03453.hp2 |
5_prime_UTR_variant | MODIFIER | c.-1070C>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | 1070 | chr22 | 27801613 | |||||
chr22:27801741
|
C | G | 1 | a0001c0001t0037 | 1 | HG04184.hp2 | 5_prime_UTR_variant | MODIFIER | c.-1198G>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/2 | 1198 | chr22 | 27801741 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:27751201
|
C | T | 43 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0076others(40): Show | 43 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.3782-105G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27751201 | ||||||
chr22:27751202
|
G | A | 3 | a0001c0001t0017g0352a0001c0001t0051g0138a0004c0007t0001g0273 | 3 | HG00099.hp1 HG01099.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.3782-106C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27751202 | ||||||
chr22:27751310
|
T | C | 43 | a0001c0001t0001g0124a0001c0001t0001g0166a0001c0001t0001g0167others(40): Show | 44 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.3782-214A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27751310 | ||||||
chr22:27751310
|
T | G | 6 | a0001c0001t0016g0110a0001c0005t0043g0037a0001c0009t0021g0006others(3): Show | 7 | HG02451.hp2 HG02895.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.3782-214A>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27751310 | ||||||
chr22:27751316
|
T | C | 9 | a0001c0001t0006g0218a0001c0001t0044g0040a0001c0001t0045g0042others(6): Show | 9 | HG01243.hp2 HG02257.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.3782-220A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27751316 | ||||||
chr22:27751387
|
T | C | 1 | a0001c0001t0052g0080 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.3782-291A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27751387 | ||||||
chr22:27751419
|
T | A | 1 | a0001c0001t0062g0063 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3782-323A>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27751419 | ||||||
chr22:27751437
|
C | T | 3 | a0001c0001t0003g0329a0001c0001t0005g0109a0002c0002t0005g0267 | 3 | NA18747.hp2 NA18947.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.3782-341G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27751437 | ||||||
chr22:27751489
|
G | A | 48 | a0001c0001t0001g0004a0001c0001t0001g0124a0001c0001t0001g0155others(45): Show | 50 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.3782-393C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27751489 | ||||||
chr22:27751492
|
G | A | 1 | a0001c0001t0002g0191 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.3782-396C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27751492 | ||||||
chr22:27751492
|
G | T | 1 | a0001c0005t0009g0017 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3782-396C>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27751492 | ||||||
chr22:27751638
|
G | A | 6 | a0001c0001t0002g0230a0001c0001t0045g0042a0001c0005t0028g0051others(3): Show | 6 | HG02257.hp1 HG03139.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.3782-542C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27751638 | ||||||
chr22:27751708
|
G | A | 2 | a0001c0014t0018g0374a0002c0003t0009g0031 | 2 | HG02257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.3782-612C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27751708 | ||||||
chr22:27751943
|
G | A | 8 | a0001c0001t0001g0146a0001c0001t0001g0221a0001c0001t0002g0132others(5): Show | 8 | HG00621.hp2 HG02074.hp2 NA18992.hp2 others(5): Show |
intron_variant | MODIFIER | c.3782-847C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27751943 | ||||||
chr22:27752310
|
G | T | 8 | a0001c0001t0002g0176a0001c0001t0058g0233a0001c0001t0059g0231others(5): Show | 8 | HG01099.hp1 HG01884.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.3782-1214C>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27752310 | ||||||
chr22:27752339
|
G | T | 1 | a0001c0001t0050g0174 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.3782-1243C>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27752339 | ||||||
chr22:27752825
|
G | A | 113 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0055others(110): Show | 116 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.3782-1729C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27752825 | ||||||
chr22:27752840
|
G | A | 1 | a0001c0001t0075g0384 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3782-1744C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27752840 | ||||||
chr22:27753072
|
G | A | 1 | a0001c0001t0069g0373 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3782-1976C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27753072 | ||||||
chr22:27753172
|
A | C | 199 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0055others(196): Show | 202 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(199): Show |
intron_variant | MODIFIER | c.3782-2076T>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27753172 | ||||||
chr22:27753215
|
C | T | 1 | a0001c0001t0005g0165 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.3782-2119G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27753215 | ||||||
chr22:27753705
|
C | A | 44 | a0001c0001t0001g0083a0001c0001t0002g0062a0001c0001t0002g0066others(41): Show | 45 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.3782-2609G>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27753705 | ||||||
chr22:27753739
|
G | A | 1 | a0001c0001t0002g0176 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3782-2643C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27753739 | ||||||
chr22:27753786
|
C | T | 10 | a0001c0001t0002g0108a0001c0001t0002g0114a0001c0001t0002g0194others(7): Show | 10 | HG00738.hp1 HG01109.hp1 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.3782-2690G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27753786 | ||||||
chr22:27753821
|
G | C | 1 | a0010c0015t0005g0045 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.3782-2725C>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27753821 | ||||||
chr22:27753843
|
C | T | 6 | a0001c0001t0001g0124a0001c0001t0002g0213a0001c0001t0068g0331others(3): Show | 6 | HG02559.hp2 HG02809.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.3782-2747G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27753843 | ||||||
chr22:27753940
|
C | T | 12 | a0001c0001t0001g0078a0001c0001t0002g0212a0001c0001t0003g0340others(9): Show | 12 | HG00673.hp1 HG00673.hp2 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.3782-2844G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27753940 | ||||||
chr22:27754010
|
C | G | 59 | a0001c0001t0001g0065a0001c0001t0001g0083a0001c0001t0001g0134others(56): Show | 61 | HG00099.hp1 HG00323.hp2 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.3782-2914G>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27754010 | ||||||
chr22:27754066
|
G | A | 5 | a0001c0005t0016g0053a0001c0013t0001g0047a0001c0013t0048g0046others(2): Show | 5 | HG01884.hp1 HG02572.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.3782-2970C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27754066 | ||||||
chr22:27754121
|
A | G | 324 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0055others(321): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.3782-3025T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27754121 | ||||||
chr22:27754221
|
G | A | 1 | a0001c0012t0001g0278 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.3782-3125C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27754221 | ||||||
chr22:27754227
|
C | T | 2 | a0001c0001t0002g0113a0002c0002t0002g0257 | 2 | NA18967.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.3782-3131G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27754227 | ||||||
chr22:27754257
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.3782-3161C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27754257 | ||||||
chr22:27754494
|
A | G | 5 | a0001c0001t0002g0116a0001c0001t0002g0230a0001c0001t0069g0373others(2): Show | 5 | HG01243.hp2 HG02055.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.3782-3398T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27754494 | ||||||
chr22:27754505
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.3782-3409C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27754505 | ||||||
chr22:27754744
|
G | A | 13 | a0001c0001t0001g0078a0001c0001t0002g0212a0001c0001t0003g0340others(10): Show | 13 | HG00673.hp1 HG00673.hp2 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.3782-3648C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27754744 | ||||||
chr22:27754756
|
G | A | 2 | a0001c0001t0027g0102a0001c0001t0027g0154 | 2 | HG00738.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.3782-3660C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27754756 | ||||||
chr22:27754826
|
C | T | 2 | a0001c0005t0043g0037a0002c0003t0014g0021 | 2 | NA19030.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3782-3730G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27754826 | ||||||
chr22:27754827
|
G | A | 57 | a0001c0001t0001g0065a0001c0001t0001g0082a0001c0001t0001g0083others(54): Show | 59 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.3782-3731C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27754827 | ||||||
chr22:27754848
|
C | A | 1 | a0001c0001t0004g0295 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.3782-3752G>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27754848 | ||||||
chr22:27754875
|
C | A | 12 | a0001c0001t0001g0078a0001c0001t0002g0212a0001c0001t0003g0340others(9): Show | 12 | HG00673.hp1 HG00673.hp2 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.3782-3779G>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27754875 | ||||||
chr22:27754978
|
C | T | 1 | a0001c0001t0011g0069 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.3782-3882G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27754978 | ||||||
chr22:27755022
|
C | A | 1 | a0003c0004t0002g0240 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3782-3926G>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27755022 | ||||||
chr22:27755132
|
C | G | 111 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0097others(108): Show | 112 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.3782-4036G>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27755132 | ||||||
chr22:27755226
|
C | A | 4 | a0001c0001t0001g0094a0001c0001t0001g0144a0001c0001t0037g0009others(1): Show | 4 | HG03704.hp1 HG03710.hp2 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.3782-4130G>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27755226 | ||||||
chr22:27755420
|
G | A | 2 | a0001c0001t0002g0176a0002c0003t0039g0028 | 2 | HG01884.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.3782-4324C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27755420 | ||||||
chr22:27755602
|
C | G | 11 | a0001c0001t0001g0078a0001c0001t0002g0212a0001c0001t0003g0340others(8): Show | 11 | HG00673.hp1 HG00673.hp2 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.3782-4506G>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27755602 | ||||||
chr22:27755645
|
C | A | 2 | a0001c0009t0006g0268a0002c0003t0009g0022 | 2 | HG02258.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.3782-4549G>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27755645 | ||||||
chr22:27755685
|
A | G | 325 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0055others(322): Show | 331 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.3782-4589T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27755685 | ||||||
chr22:27755729
|
C | T | 4 | a0001c0001t0002g0070a0001c0001t0002g0232a0001c0009t0006g0268others(1): Show | 4 | HG01192.hp2 HG01891.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.3782-4633G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27755729 | ||||||
chr22:27755801
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.3782-4705C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27755801 | ||||||
chr22:27755837
|
G | A | 76 | a0001c0001t0001g0001a0001c0001t0001g0055a0001c0001t0001g0061others(73): Show | 77 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.3782-4741C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27755837 | ||||||
chr22:27755839
|
G | A | 6 | a0001c0001t0001g0134a0001c0001t0060g0171a0001c0001t0074g0385others(3): Show | 6 | HG01496.hp1 HG02280.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.3782-4743C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27755839 | ||||||
chr22:27755883
|
T | C | 6 | a0001c0001t0001g0134a0001c0001t0060g0171a0001c0001t0074g0385others(3): Show | 6 | HG01496.hp1 HG02280.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.3782-4787A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27755883 | ||||||
chr22:27755977
|
G | A | 3 | a0001c0001t0001g0083a0001c0001t0001g0137a0001c0001t0001g0219 | 3 | HG01123.hp1 HG02273.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.3782-4881C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27755977 | ||||||
chr22:27756213
|
T | C | 2 | a0001c0001t0005g0084a0001c0001t0005g0153 | 2 | HG01358.hp1 HG01928.hp1 |
intron_variant | MODIFIER | c.3782-5117A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27756213 | ||||||
chr22:27756254
|
G | A | 3 | a0001c0001t0001g0107a0001c0001t0002g0117a0001c0001t0007g0118 | 3 | HG00438.hp1 NA18959.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.3782-5158C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27756254 | ||||||
chr22:27756281
|
T | G | 1 | a0001c0016t0003g0280 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.3782-5185A>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27756281 | ||||||
chr22:27756370
|
C | A | 1 | a0001c0001t0004g0281 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.3782-5274G>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27756370 | ||||||
chr22:27756385
|
G | A | 9 | a0001c0001t0001g0235a0001c0001t0002g0057a0001c0001t0002g0125others(6): Show | 9 | HG01891.hp2 HG02630.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.3782-5289C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27756385 | ||||||
chr22:27756613
|
G | A | 130 | a0001c0001t0001g0003a0001c0001t0001g0078a0001c0001t0001g0079others(127): Show | 131 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.3782-5517C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27756613 | ||||||
chr22:27756648
|
G | A | 1 | a0001c0005t0016g0053 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3782-5552C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27756648 | ||||||
chr22:27756651
|
A | G | 75 | a0001c0001t0001g0001a0001c0001t0001g0055a0001c0001t0001g0061others(72): Show | 76 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.3782-5555T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27756651 | ||||||
chr22:27756810
|
C | T | 4 | a0001c0001t0002g0108a0001c0001t0002g0194a0001c0001t0024g0018others(1): Show | 4 | HG02683.hp2 HG02735.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.3782-5714G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27756810 | ||||||
chr22:27756868
|
A | C | 1 | a0001c0005t0016g0053 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3782-5772T>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27756868 | ||||||
chr22:27757178
|
G | A | 2 | a0001c0001t0002g0230a0002c0003t0014g0034 | 2 | HG01243.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.3782-6082C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27757178 | ||||||
chr22:27757252
|
C | G | 1 | a0002c0002t0006g0266 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.3782-6156G>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27757252 | ||||||
chr22:27757334
|
G | C | 13 | a0001c0001t0001g0078a0001c0001t0002g0212a0001c0001t0003g0340others(10): Show | 13 | HG00673.hp1 HG00673.hp2 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.3782-6238C>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27757334 | ||||||
chr22:27757349
|
G | A | 2 | a0001c0005t0043g0037a0002c0003t0014g0021 | 2 | NA19030.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3782-6253C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27757349 | ||||||
chr22:27757691
|
G | A | 1 | a0001c0001t0057g0237 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3782-6595C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27757691 | ||||||
chr22:27757802
|
C | T | 2 | a0001c0001t0001g0158a0001c0001t0006g0159 | 2 | NA18983.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.3782-6706G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27757802 | ||||||
chr22:27757813
|
T | C | 1 | a0001c0001t0032g0360 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.3782-6717A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27757813 | ||||||
chr22:27757868
|
A | C | 326 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0055others(323): Show | 331 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.3782-6772T>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27757868 | ||||||
chr22:27758150
|
C | T | 4 | a0001c0001t0001g0134a0001c0005t0009g0016a0001c0010t0024g0013others(1): Show | 4 | HG01496.hp1 HG02280.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.3782-7054G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27758150 | ||||||
chr22:27758218
|
G | A | 1 | a0002c0003t0015g0023 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3782-7122C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27758218 | ||||||
chr22:27758378
|
T | C | 13 | a0001c0001t0001g0078a0001c0001t0002g0212a0001c0001t0003g0340others(10): Show | 13 | HG00673.hp1 HG00673.hp2 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.3782-7282A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27758378 | ||||||
chr22:27758622
|
C | G | 13 | a0001c0001t0001g0078a0001c0001t0002g0212a0001c0001t0003g0340others(10): Show | 13 | HG00673.hp1 HG00673.hp2 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.3782-7526G>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27758622 | ||||||
chr22:27758630
|
G | T | 309 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0055others(306): Show | 313 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(310): Show |
intron_variant | MODIFIER | c.3782-7534C>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27758630 | ||||||
chr22:27758665
|
C | T | 13 | a0001c0001t0001g0078a0001c0001t0002g0212a0001c0001t0003g0340others(10): Show | 13 | HG00673.hp1 HG00673.hp2 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.3782-7569G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27758665 | ||||||
chr22:27758671
|
C | T | 13 | a0001c0001t0001g0078a0001c0001t0002g0212a0001c0001t0003g0340others(10): Show | 13 | HG00673.hp1 HG00673.hp2 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.3782-7575G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27758671 | ||||||
chr22:27758754
|
C | T | 1 | a0001c0001t0069g0373 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3782-7658G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27758754 | ||||||
chr22:27758961
|
G | T | 1 | a0002c0003t0019g0033 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3782-7865C>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27758961 | ||||||
chr22:27759000
|
A | G | 13 | a0001c0001t0001g0078a0001c0001t0002g0212a0001c0001t0003g0340others(10): Show | 13 | HG00673.hp1 HG00673.hp2 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.3782-7904T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27759000 | ||||||
chr22:27759197
|
C | A | 4 | a0001c0013t0001g0047a0001c0013t0048g0046a0002c0003t0015g0025others(1): Show | 4 | HG01884.hp1 HG02572.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.3782-8101G>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27759197 | ||||||
chr22:27759212
|
C | G | 4 | a0001c0001t0001g0119a0001c0001t0001g0157a0001c0001t0003g0309others(1): Show | 4 | HG00558.hp1 HG00609.hp1 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.3782-8116G>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27759212 | ||||||
chr22:27759235
|
G | A | 13 | a0001c0001t0001g0078a0001c0001t0002g0212a0001c0001t0003g0340others(10): Show | 13 | HG00673.hp1 HG00673.hp2 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.3782-8139C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27759235 | ||||||
chr22:27759241
|
G | A | 8 | a0001c0001t0001g0141a0001c0001t0001g0149a0001c0001t0001g0195others(5): Show | 8 | HG01168.hp1 HG01928.hp2 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.3782-8145C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27759241 | ||||||
chr22:27759309
|
C | A | 1 | a0001c0005t0016g0053 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3782-8213G>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27759309 | ||||||
chr22:27759344
|
CAA | C | 11 | a0001c0001t0001g0148a0001c0001t0001g0220a0001c0001t0001g0227others(8): Show | 11 | HG00280.hp2 HG01106.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.3782-8250_3782-824 others(6): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27759344 | ||||||
chr22:27759361
|
G | A | 1 | a0001c0005t0009g0017 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3782-8265C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27759361 | ||||||
chr22:27759416
|
C | T | 22 | a0001c0001t0002g0059a0001c0001t0002g0066a0001c0001t0002g0163others(19): Show | 22 | HG00323.hp2 HG00639.hp2 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.3782-8320G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27759416 | ||||||
chr22:27759458
|
C | T | 1 | a0002c0002t0002g0263 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.3782-8362G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27759458 | ||||||
chr22:27759459
|
G | A | 13 | a0001c0001t0001g0078a0001c0001t0002g0212a0001c0001t0003g0340others(10): Show | 13 | HG00673.hp1 HG00673.hp2 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.3782-8363C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27759459 | ||||||
chr22:27759464
|
G | A | 138 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0081others(135): Show | 140 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(137): Show |
intron_variant | MODIFIER | c.3782-8368C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27759464 | ||||||
chr22:27759468
|
C | T | 15 | a0001c0001t0001g0235a0001c0001t0002g0057a0001c0001t0002g0125others(12): Show | 15 | HG01891.hp2 HG02145.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.3782-8372G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27759468 | ||||||
chr22:27759689
|
C | A | 2 | a0001c0001t0004g0353a0001c0001t0034g0327 | 2 | HG00423.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.3782-8593G>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27759689 | ||||||
chr22:27759842
|
TG | T | 13 | a0001c0001t0001g0078a0001c0001t0002g0212a0001c0001t0003g0340others(10): Show | 13 | HG00673.hp1 HG00673.hp2 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.3782-8747delC | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27759842 | ||||||
chr22:27759975
|
TG | T | 11 | a0001c0001t0001g0148a0001c0001t0001g0220a0001c0001t0001g0227others(8): Show | 11 | HG00280.hp2 HG01106.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.3782-8880delC | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27759975 | ||||||
chr22:27759999
|
C | T | 2 | a0001c0014t0018g0374a0002c0003t0009g0031 | 2 | HG02257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.3782-8903G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27759999 | ||||||
chr22:27760004
|
G | A | 17 | a0001c0001t0001g0235a0001c0001t0002g0057a0001c0001t0002g0125others(14): Show | 17 | HG01891.hp2 HG02145.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.3782-8908C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27760004 | ||||||
chr22:27760075
|
C | T | 2 | a0001c0005t0043g0037a0002c0003t0014g0021 | 2 | NA19030.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3782-8979G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27760075 | ||||||
chr22:27760430
|
GC | G | 4 | a0001c0013t0001g0047a0001c0013t0048g0046a0002c0003t0015g0025others(1): Show | 4 | HG01884.hp1 HG02572.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.3782-9335delG | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27760430 | ||||||
chr22:27760509
|
T | TA | 160 | a0001c0001t0001g0003a0001c0001t0001g0078a0001c0001t0001g0079others(157): Show | 162 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(159): Show |
intron_variant | MODIFIER | c.3782-9414dupT | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27760509 | ||||||
chr22:27760518
|
T | G | 1 | a0013c0024t0009g0036 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.3782-9422A>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27760518 | ||||||
chr22:27760720
|
G | A | 1 | a0001c0001t0069g0373 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3782-9624C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27760720 | ||||||
chr22:27760728
|
A | C | 1 | a0001c0001t0026g0044 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.3782-9632T>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27760728 | ||||||
chr22:27760800
|
A | G | 147 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0081others(144): Show | 149 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(146): Show |
intron_variant | MODIFIER | c.3782-9704T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27760800 | ||||||
chr22:27760869
|
C | T | 1 | a0002c0003t0014g0029 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3782-9773G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27760869 | ||||||
chr22:27761048
|
C | T | 1 | a0001c0001t0002g0108 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.3782-9952G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27761048 | ||||||
chr22:27761218
|
T | C | 79 | a0001c0001t0001g0001a0001c0001t0001g0055a0001c0001t0001g0061others(76): Show | 80 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.3782-10122A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27761218 | ||||||
chr22:27761221
|
T | TTC | 13 | a0001c0001t0001g0078a0001c0001t0002g0212a0001c0001t0003g0340others(10): Show | 13 | HG00673.hp1 HG00673.hp2 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.3782-10127_3782-10 others(8): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27761221 | ||||||
chr22:27761313
|
T | C | 33 | a0001c0001t0001g0148a0001c0001t0001g0220a0001c0001t0001g0227others(30): Show | 33 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.3782-10217A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27761313 | ||||||
chr22:27761413
|
T | A | 3 | a0001c0001t0001g0119a0001c0001t0003g0309a0001c0001t0003g0355 | 3 | HG00558.hp1 HG02027.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.3782-10317A>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27761413 | ||||||
chr22:27761427
|
TG | T | 14 | a0001c0001t0001g0078a0001c0001t0002g0212a0001c0001t0003g0340others(11): Show | 14 | HG00673.hp1 HG00673.hp2 HG02015.hp1 others(11): Show |
intron_variant | MODIFIER | c.3782-10332delC | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27761427 | ||||||
chr22:27761432
|
G | A | 2 | a0001c0005t0043g0037a0002c0003t0014g0021 | 2 | NA19030.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3782-10336C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27761432 | ||||||
chr22:27761432
|
GA | G | 121 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0083others(118): Show | 122 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.3782-10337delT | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27761432 | ||||||
chr22:27761433
|
A | G | 30 | a0001c0001t0001g0148a0001c0001t0001g0157a0001c0001t0001g0220others(27): Show | 30 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.3782-10337T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27761433 | ||||||
chr22:27761434
|
A | G | 1 | a0001c0001t0062g0063 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3782-10338T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27761434 | ||||||
chr22:27761611
|
G | A | 2 | a0001c0001t0001g0180a0001c0001t0003g0319 | 2 | HG03654.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.3782-10515C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27761611 | ||||||
chr22:27761748
|
G | A | 3 | a0001c0001t0007g0112a0001c0001t0008g0200a0001c0001t0010g0308 | 3 | HG02486.hp1 NA20752.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.3782-10652C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27761748 | ||||||
chr22:27761753
|
G | A | 2 | a0001c0001t0030g0169a0004c0007t0001g0273 | 2 | HG01167.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.3782-10657C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27761753 | ||||||
chr22:27761760
|
C | T | 2 | a0001c0001t0008g0067a0002c0002t0031g0371 | 2 | HG00280.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.3782-10664G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27761760 | ||||||
chr22:27761768
|
G | A | 5 | a0001c0001t0003g0290a0001c0013t0001g0047a0001c0013t0048g0046others(2): Show | 5 | HG01884.hp1 HG02572.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.3782-10672C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27761768 | ||||||
chr22:27761852
|
A | G | 1 | a0001c0005t0002g0048 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3782-10756T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27761852 | ||||||
chr22:27761882
|
G | A | 5 | a0001c0001t0009g0020a0001c0005t0049g0052a0001c0008t0018g0376others(2): Show | 5 | HG02145.hp1 HG02451.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.3782-10786C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27761882 | ||||||
chr22:27761982
|
T | C | 13 | a0001c0001t0001g0078a0001c0001t0002g0212a0001c0001t0003g0340others(10): Show | 13 | HG00673.hp1 HG00673.hp2 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.3782-10886A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27761982 | ||||||
chr22:27762026
|
G | T | 13 | a0001c0001t0001g0078a0001c0001t0002g0212a0001c0001t0003g0340others(10): Show | 13 | HG00673.hp1 HG00673.hp2 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.3782-10930C>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27762026 | ||||||
chr22:27762066
|
C | A | 13 | a0001c0001t0001g0078a0001c0001t0002g0212a0001c0001t0003g0340others(10): Show | 13 | HG00673.hp1 HG00673.hp2 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.3782-10970G>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27762066 | ||||||
chr22:27762071
|
G | C | 1 | a0001c0001t0001g0094 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.3782-10975C>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27762071 | ||||||
chr22:27762073
|
A | G | 13 | a0001c0001t0001g0078a0001c0001t0002g0212a0001c0001t0003g0340others(10): Show | 13 | HG00673.hp1 HG00673.hp2 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.3782-10977T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27762073 | ||||||
chr22:27762131
|
T | C | 1 | a0003c0004t0001g0247 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3782-11035A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27762131 | ||||||
chr22:27762187
|
T | A | 16 | a0001c0001t0001g0183a0001c0001t0002g0086a0001c0001t0002g0191others(13): Show | 16 | HG00423.hp1 HG02071.hp1 NA18940.hp1 others(13): Show |
intron_variant | MODIFIER | c.3782-11091A>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27762187 | ||||||
chr22:27762258
|
C | T | 1 | a0001c0012t0001g0278 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.3782-11162G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27762258 | ||||||
chr22:27762297
|
A | G | 2 | a0001c0001t0002g0176a0002c0003t0039g0028 | 2 | HG01884.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.3782-11201T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27762297 | ||||||
chr22:27762369
|
A | C | 1 | a0001c0001t0003g0306 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.3782-11273T>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27762369 | ||||||
chr22:27762426
|
C | T | 16 | a0001c0001t0002g0062a0001c0001t0002g0114a0001c0001t0002g0206others(13): Show | 16 | HG00735.hp2 HG00738.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.3782-11330G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27762426 | ||||||
chr22:27762555
|
C | G | 1 | a0001c0001t0062g0063 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3782-11459G>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27762555 | ||||||
chr22:27762586
|
T | C | 3 | a0001c0001t0033g0287a0001c0001t0033g0318a0001c0001t0061g0222 | 3 | HG02109.hp1 HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.3782-11490A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27762586 | ||||||
chr22:27762602
|
C | T | 1 | a0003c0004t0002g0242 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.3782-11506G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27762602 | ||||||
chr22:27762612
|
C | T | 1 | a0001c0005t0016g0053 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3782-11516G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27762612 | ||||||
chr22:27762661
|
C | T | 31 | a0001c0001t0001g0074a0001c0001t0001g0082a0001c0001t0001g0083others(28): Show | 32 | HG00438.hp2 HG00621.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.3782-11565G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27762661 | ||||||
chr22:27762722
|
C | T | 22 | a0001c0001t0001g0157a0001c0001t0002g0059a0001c0001t0002g0066others(19): Show | 22 | HG00323.hp2 HG00609.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.3782-11626G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27762722 | ||||||
chr22:27762756
|
G | A | 2 | a0001c0009t0021g0006a0003c0004t0016g0248 | 3 | HG02451.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3782-11660C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27762756 | ||||||
chr22:27762820
|
C | T | 17 | a0001c0001t0001g0157a0001c0001t0002g0059a0001c0001t0002g0066others(14): Show | 17 | HG00323.hp2 HG00609.hp1 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.3782-11724G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27762820 | ||||||
chr22:27762865
|
G | A | 13 | a0001c0001t0001g0078a0001c0001t0002g0212a0001c0001t0003g0340others(10): Show | 13 | HG00673.hp1 HG00673.hp2 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.3782-11769C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27762865 | ||||||
chr22:27762879
|
G | GCTTGAGC others(1): Show |
8 | a0001c0001t0001g0134a0001c0001t0021g0073a0001c0001t0059g0231others(5): Show | 8 | HG01496.hp1 HG02280.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.3782-11791_3782-11 others(14): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27762879 | ||||||
chr22:27762924
|
C | T | 15 | a0001c0001t0002g0062a0001c0001t0002g0114a0001c0001t0002g0206others(12): Show | 15 | HG00735.hp2 HG00738.hp1 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.3782-11828G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27762924 | ||||||
chr22:27762925
|
G | A | 1 | a0001c0001t0002g0230 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3782-11829C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27762925 | ||||||
chr22:27762930
|
C | G | 1 | a0001c0001t0003g0320 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.3782-11834G>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27762930 | ||||||
chr22:27762998
|
C | T | 1 | a0001c0001t0011g0120 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.3782-11902G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27762998 | ||||||
chr22:27763022
|
G | C | 2 | a0001c0005t0043g0037a0002c0003t0014g0021 | 2 | NA19030.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3782-11926C>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27763022 | ||||||
chr22:27763097
|
AAAAACAA others(3): Show |
A | 5 | a0001c0001t0002g0130a0001c0001t0006g0135a0001c0001t0010g0323others(2): Show | 5 | NA18942.hp1 NA18951.hp2 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.3782-12011_3782-12 others(16): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27763097 | ||||||
chr22:27763126
|
T | C | 1 | a0001c0001t0002g0156 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.3782-12030A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27763126 | ||||||
chr22:27763240
|
C | T | 3 | a0001c0001t0076g0386a0002c0003t0019g0032a0002c0003t0019g0033 | 3 | HG01496.hp2 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.3782-12144G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27763240 | ||||||
chr22:27763323
|
C | T | 8 | a0001c0001t0001g0134a0001c0001t0002g0176a0001c0001t0021g0073others(5): Show | 8 | HG01496.hp1 HG02280.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.3782-12227G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27763323 | ||||||
chr22:27763359
|
C | T | 13 | a0001c0001t0001g0078a0001c0001t0002g0212a0001c0001t0003g0340others(10): Show | 13 | HG00673.hp1 HG00673.hp2 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.3782-12263G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27763359 | ||||||
chr22:27763372
|
G | A | 2 | a0001c0001t0007g0173a0001c0001t0022g0333 | 2 | NA18612.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.3782-12276C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27763372 | ||||||
chr22:27763388
|
G | A | 12 | a0001c0001t0001g0148a0001c0001t0001g0193a0001c0001t0001g0220others(9): Show | 12 | HG00280.hp2 HG01106.hp1 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.3782-12292C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27763388 | ||||||
chr22:27763497
|
A | T | 13 | a0001c0001t0001g0078a0001c0001t0002g0212a0001c0001t0003g0340others(10): Show | 13 | HG00673.hp1 HG00673.hp2 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.3782-12401T>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27763497 | ||||||
chr22:27763546
|
T | G | 12 | a0001c0001t0001g0148a0001c0001t0001g0193a0001c0001t0001g0220others(9): Show | 12 | HG00280.hp2 HG01106.hp1 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.3782-12450A>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27763546 | ||||||
chr22:27763555
|
G | T | 13 | a0001c0001t0001g0078a0001c0001t0002g0212a0001c0001t0003g0340others(10): Show | 13 | HG00673.hp1 HG00673.hp2 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.3782-12459C>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27763555 | ||||||
chr22:27763623
|
C | T | 13 | a0001c0001t0001g0078a0001c0001t0002g0212a0001c0001t0003g0340others(10): Show | 13 | HG00673.hp1 HG00673.hp2 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.3782-12527G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27763623 | ||||||
chr22:27763661
|
G | A | 3 | a0001c0001t0011g0142a0001c0001t0011g0168a0002c0002t0001g0264 | 3 | HG00423.hp1 NA19000.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.3782-12565C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27763661 | ||||||
chr22:27763674
|
A | T | 1 | a0002c0003t0014g0029 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3782-12578T>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27763674 | ||||||
chr22:27763684
|
G | A | 224 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0055others(221): Show | 227 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.3782-12588C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27763684 | ||||||
chr22:27763702
|
T | C | 318 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0055others(315): Show | 322 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(319): Show |
intron_variant | MODIFIER | c.3782-12606A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27763702 | ||||||
chr22:27763760
|
T | C | 226 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0055others(223): Show | 229 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(226): Show |
intron_variant | MODIFIER | c.3782-12664A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27763760 | ||||||
chr22:27763806
|
A | C | 13 | a0001c0001t0001g0078a0001c0001t0002g0212a0001c0001t0003g0340others(10): Show | 13 | HG00673.hp1 HG00673.hp2 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.3782-12710T>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27763806 | ||||||
chr22:27763818
|
G | A | 1 | a0001c0001t0064g0302 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.3782-12722C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27763818 | ||||||
chr22:27763874
|
G | C | 13 | a0001c0001t0001g0078a0001c0001t0002g0212a0001c0001t0003g0340others(10): Show | 13 | HG00673.hp1 HG00673.hp2 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.3782-12778C>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27763874 | ||||||
chr22:27763915
|
C | G | 13 | a0001c0001t0001g0078a0001c0001t0002g0212a0001c0001t0003g0340others(10): Show | 13 | HG00673.hp1 HG00673.hp2 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.3782-12819G>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27763915 | ||||||
chr22:27763929
|
G | A | 1 | a0001c0012t0001g0277 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.3782-12833C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27763929 | ||||||
chr22:27763952
|
A | G | 1 | a0001c0001t0053g0123 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3782-12856T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27763952 | ||||||
chr22:27763971
|
C | T | 13 | a0001c0001t0001g0078a0001c0001t0002g0212a0001c0001t0003g0340others(10): Show | 13 | HG00673.hp1 HG00673.hp2 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.3782-12875G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27763971 | ||||||
chr22:27764059
|
G | C | 17 | a0001c0001t0001g0235a0001c0001t0002g0057a0001c0001t0002g0125others(14): Show | 17 | HG01891.hp2 HG02145.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.3782-12963C>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27764059 | ||||||
chr22:27764062
|
G | A | 13 | a0001c0001t0001g0078a0001c0001t0002g0212a0001c0001t0003g0340others(10): Show | 13 | HG00673.hp1 HG00673.hp2 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.3782-12966C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27764062 | ||||||
chr22:27764086
|
T | C | 320 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0055others(317): Show | 324 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(321): Show |
intron_variant | MODIFIER | c.3782-12990A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27764086 | ||||||
chr22:27764110
|
C | A | 1 | a0001c0001t0022g0333 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.3782-13014G>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27764110 | ||||||
chr22:27764112
|
G | T | 4 | a0001c0013t0001g0047a0001c0013t0048g0046a0002c0003t0015g0025others(1): Show | 4 | HG01884.hp1 HG02572.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.3782-13016C>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27764112 | ||||||
chr22:27764201
|
C | T | 2 | a0001c0005t0043g0037a0002c0003t0014g0021 | 2 | NA19030.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3782-13105G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27764201 | ||||||
chr22:27764222
|
G | A | 4 | a0001c0013t0001g0047a0001c0013t0048g0046a0002c0003t0015g0025others(1): Show | 4 | HG01884.hp1 HG02572.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.3782-13126C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27764222 | ||||||
chr22:27764353
|
C | T | 13 | a0001c0001t0001g0078a0001c0001t0002g0212a0001c0001t0003g0340others(10): Show | 13 | HG00673.hp1 HG00673.hp2 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.3782-13257G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27764353 | ||||||
chr22:27764419
|
C | T | 229 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0055others(226): Show | 232 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(229): Show |
intron_variant | MODIFIER | c.3782-13323G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27764419 | ||||||
chr22:27764551
|
C | T | 1 | a0001c0001t0001g0083 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.3782-13455G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27764551 | ||||||
chr22:27764755
|
G | A | 1 | a0001c0001t0053g0123 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3782-13659C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27764755 | ||||||
chr22:27764855
|
G | A | 13 | a0001c0001t0001g0078a0001c0001t0002g0212a0001c0001t0003g0340others(10): Show | 13 | HG00673.hp1 HG00673.hp2 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.3782-13759C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27764855 | ||||||
chr22:27764984
|
T | G | 317 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0055others(314): Show | 321 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(318): Show |
intron_variant | MODIFIER | c.3782-13888A>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27764984 | ||||||
chr22:27764996
|
G | C | 212 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0055others(209): Show | 215 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.3782-13900C>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27764996 | ||||||
chr22:27765038
|
T | C | 1 | a0001c0001t0002g0095 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.3782-13942A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27765038 | ||||||
chr22:27765158
|
C | T | 1 | a0001c0001t0025g0041 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3782-14062G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27765158 | ||||||
chr22:27765181
|
T | G | 1 | a0001c0001t0004g0358 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.3782-14085A>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27765181 | ||||||
chr22:27765249
|
T | C | 14 | a0001c0001t0001g0078a0001c0001t0002g0212a0001c0001t0003g0340others(11): Show | 14 | HG00673.hp1 HG00673.hp2 HG02015.hp1 others(11): Show |
intron_variant | MODIFIER | c.3782-14153A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27765249 | ||||||
chr22:27765370
|
A | G | 1 | a0001c0001t0057g0237 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3782-14274T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27765370 | ||||||
chr22:27765422
|
AG | A | 251 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0055others(248): Show | 254 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.3782-14327delC | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27765422 | ||||||
chr22:27765423
|
G | A | 16 | a0001c0001t0001g0078a0001c0001t0002g0212a0001c0001t0003g0306others(13): Show | 16 | HG00673.hp1 HG00673.hp2 HG02015.hp1 others(13): Show |
intron_variant | MODIFIER | c.3782-14327C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27765423 | ||||||
chr22:27765509
|
C | T | 7 | a0001c0001t0001g0124a0001c0001t0002g0213a0001c0001t0023g0019others(4): Show | 7 | HG02559.hp2 HG02809.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.3782-14413G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27765509 | ||||||
chr22:27765553
|
C | G | 1 | a0001c0005t0016g0053 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3782-14457G>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27765553 | ||||||
chr22:27765715
|
A | G | 72 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0074others(69): Show | 73 | HG00323.hp2 HG00438.hp2 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.3782-14619T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27765715 | ||||||
chr22:27765817
|
G | C | 13 | a0001c0001t0001g0187a0001c0001t0001g0193a0001c0001t0001g0195others(10): Show | 13 | HG00280.hp2 HG01106.hp1 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.3782-14721C>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27765817 | ||||||
chr22:27765909
|
C | T | 1 | a0001c0001t0005g0170 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.3782-14813G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27765909 | ||||||
chr22:27765943
|
C | T | 4 | a0001c0001t0001g0061a0001c0001t0002g0226a0002c0002t0017g0364others(1): Show | 4 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.3782-14847G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27765943 | ||||||
chr22:27766105
|
C | T | 1 | a0001c0001t0005g0085 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.3782-15009G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27766105 | ||||||
chr22:27766116
|
T | C | 1 | a0001c0001t0053g0123 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3782-15020A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27766116 | ||||||
chr22:27766152
|
C | T | 21 | a0001c0001t0001g0235a0001c0001t0002g0057a0001c0001t0002g0125others(18): Show | 21 | HG01884.hp1 HG01891.hp2 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.3782-15056G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27766152 | ||||||
chr22:27766825
|
C | T | 1 | a0001c0001t0058g0233 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.3782-15729G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27766825 | ||||||
chr22:27766826
|
G | A | 2 | a0001c0005t0043g0037a0002c0003t0014g0021 | 2 | NA19030.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3782-15730C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27766826 | ||||||
chr22:27766859
|
G | A | 1 | a0001c0001t0045g0042 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3782-15763C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27766859 | ||||||
chr22:27766870
|
G | A | 1 | a0001c0001t0002g0106 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.3782-15774C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27766870 | ||||||
chr22:27766995
|
G | T | 1 | a0001c0010t0040g0012 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3782-15899C>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27766995 | ||||||
chr22:27767046
|
A | T | 1 | a0001c0001t0024g0018 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.3782-15950T>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27767046 | ||||||
chr22:27767211
|
C | G | 1 | a0002c0003t0042g0030 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3782-16115G>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27767211 | ||||||
chr22:27767264
|
G | A | 2 | a0001c0001t0001g0183a0001c0001t0003g0316 | 2 | NA18981.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.3782-16168C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27767264 | ||||||
chr22:27767358
|
G | A | 80 | a0001c0001t0001g0001a0001c0001t0001g0055a0001c0001t0001g0071others(77): Show | 81 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.3782-16262C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27767358 | ||||||
chr22:27767475
|
C | A | 1 | a0002c0003t0015g0026 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3782-16379G>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27767475 | ||||||
chr22:27767621
|
T | C | 3 | a0001c0001t0009g0020a0001c0008t0018g0376a0001c0014t0018g0375 | 3 | HG02145.hp1 HG03130.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.3782-16525A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27767621 | ||||||
chr22:27767710
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.3782-16614G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27767710 | ||||||
chr22:27767715
|
C | T | 1 | a0001c0001t0010g0322 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.3782-16619G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27767715 | ||||||
chr22:27767782
|
G | T | 2 | a0001c0005t0043g0037a0002c0003t0014g0021 | 2 | NA19030.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3782-16686C>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27767782 | ||||||
chr22:27767811
|
A | G | 16 | a0001c0001t0001g0148a0001c0001t0002g0062a0001c0001t0002g0114others(13): Show | 16 | HG00735.hp2 HG00738.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.3782-16715T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27767811 | ||||||
chr22:27767979
|
G | A | 1 | a0002c0002t0001g0265 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.3782-16883C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27767979 | ||||||
chr22:27768006
|
A | G | 135 | a0001c0001t0001g0003a0001c0001t0001g0078a0001c0001t0001g0107others(132): Show | 137 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.3782-16910T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27768006 | ||||||
chr22:27768062
|
T | G | 102 | a0001c0001t0001g0003a0001c0001t0001g0107a0001c0001t0001g0139others(99): Show | 103 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.3782-16966A>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27768062 | ||||||
chr22:27768081
|
G | C | 7 | a0001c0001t0001g0124a0001c0001t0002g0213a0001c0001t0059g0231others(4): Show | 7 | HG02559.hp2 HG02717.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.3782-16985C>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27768081 | ||||||
chr22:27768218
|
A | C | 3 | a0001c0001t0023g0019a0001c0001t0069g0373a0001c0013t0001g0047 | 3 | HG02055.hp2 HG02896.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.3782-17122T>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27768218 | ||||||
chr22:27768262
|
T | C | 4 | a0001c0001t0001g0141a0001c0001t0002g0225a0001c0001t0020g0143others(1): Show | 4 | HG01952.hp2 HG01978.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.3782-17166A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27768262 | ||||||
chr22:27768546
|
C | A | 2 | a0001c0001t0001g0195a0001c0001t0008g0092 | 2 | HG01928.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.3782-17450G>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27768546 | ||||||
chr22:27768591
|
G | A | 5 | a0001c0001t0001g0065a0001c0001t0017g0351a0001c0001t0017g0352others(2): Show | 6 | HG00099.hp1 HG01099.hp2 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.3782-17495C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27768591 | ||||||
chr22:27768640
|
T | A | 1 | a0001c0001t0002g0095 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.3782-17544A>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27768640 | ||||||
chr22:27768803
|
C | T | 1 | a0001c0001t0069g0373 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3782-17707G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27768803 | ||||||
chr22:27768824
|
T | G | 1 | a0001c0001t0001g0093 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3782-17728A>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27768824 | ||||||
chr22:27768864
|
C | T | 3 | a0001c0001t0023g0019a0001c0001t0069g0373a0001c0013t0001g0047 | 3 | HG02055.hp2 HG02896.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.3782-17768G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27768864 | ||||||
chr22:27769015
|
T | C | 21 | a0001c0001t0001g0157a0001c0001t0002g0059a0001c0001t0002g0066others(18): Show | 21 | HG00323.hp2 HG00609.hp1 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.3782-17919A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27769015 | ||||||
chr22:27769113
|
T | G | 13 | a0001c0001t0001g0097a0001c0001t0001g0187a0001c0001t0001g0193others(10): Show | 13 | HG00280.hp2 HG01106.hp1 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.3782-18017A>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27769113 | ||||||
chr22:27769346
|
A | G | 226 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0055others(223): Show | 229 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(226): Show |
intron_variant | MODIFIER | c.3782-18250T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27769346 | ||||||
chr22:27769430
|
T | C | 3 | a0001c0001t0023g0019a0001c0001t0069g0373a0001c0013t0001g0047 | 3 | HG02055.hp2 HG02896.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.3782-18334A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27769430 | ||||||
chr22:27769552
|
A | ATTTTTTT others(2): Show |
29 | a0001c0001t0001g0097a0001c0001t0001g0148a0001c0001t0001g0187others(26): Show | 29 | HG00438.hp1 HG00558.hp2 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.3782-18465_3782-18 others(15): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27769552 | ||||||
chr22:27769552
|
A | ATTTTTTT others(3): Show |
106 | a0001c0001t0001g0003a0001c0001t0001g0078a0001c0001t0001g0107others(103): Show | 107 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.3782-18466_3782-18 others(16): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27769552 | ||||||
chr22:27769552
|
A | ATTTTTTT others(4): Show |
74 | a0001c0001t0001g0001a0001c0001t0001g0055a0001c0001t0001g0072others(71): Show | 75 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.3782-18467_3782-18 others(17): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27769552 | ||||||
chr22:27769552
|
A | ATTTTTTT others(5): Show |
32 | a0001c0001t0001g0061a0001c0001t0001g0071a0001c0001t0001g0098others(29): Show | 33 | HG00408.hp1 HG00609.hp2 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.3782-18468_3782-18 others(18): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27769552 | ||||||
chr22:27769552
|
A | ATTTTTTT others(6): Show |
37 | a0001c0001t0001g0094a0001c0001t0001g0124a0001c0001t0001g0152others(34): Show | 40 | HG00735.hp1 HG01081.hp1 HG01167.hp1 others(37): Show |
intron_variant | MODIFIER | c.3782-18469_3782-18 others(19): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27769552 | ||||||
chr22:27769552
|
A | ATTTTTTT others(7): Show |
41 | a0001c0001t0001g0004a0001c0001t0001g0064a0001c0001t0001g0065others(38): Show | 42 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.3782-18470_3782-18 others(20): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27769552 | ||||||
chr22:27769552
|
A | ATTTTTTT others(8): Show |
3 | a0001c0001t0001g0155a0001c0001t0002g0202a0001c0001t0003g0338 | 3 | HG00140.hp2 HG00639.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.3782-18471_3782-18 others(21): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27769552 | ||||||
chr22:27769552
|
A | ATTTTTTT others(13): Show |
2 | a0001c0001t0053g0123a0001c0005t0016g0053 | 2 | HG03486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.3782-18457_3782-18 others(26): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27769552 | ||||||
chr22:27769552
|
A | ATTTTTTT others(14): Show |
1 | a0001c0021t0007g0250 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3782-18457_3782-18 others(27): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27769552 | ||||||
chr22:27769570
|
TGAGACAG others(32): Show |
T | 2 | a0001c0001t0023g0019a0001c0001t0069g0373 | 2 | HG02055.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.3782-18513_3782-18 others(45): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27769570 | ||||||
chr22:27769573
|
GACAGAGT others(33): Show |
G | 1 | a0001c0013t0001g0047 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.3782-18517_3782-18 others(46): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27769573 | ||||||
chr22:27769612
|
G | A | 2 | a0001c0001t0023g0019a0001c0001t0069g0373 | 2 | HG02055.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.3782-18516C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27769612 | ||||||
chr22:27769613
|
C | G | 2 | a0001c0001t0023g0019a0001c0001t0069g0373 | 2 | HG02055.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.3782-18517G>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27769613 | ||||||
chr22:27769709
|
C | T | 15 | a0001c0001t0001g0078a0001c0001t0002g0212a0001c0001t0003g0306others(12): Show | 15 | HG00673.hp1 HG00673.hp2 HG02015.hp1 others(12): Show |
intron_variant | MODIFIER | c.3782-18613G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27769709 | ||||||
chr22:27769720
|
T | A | 1 | a0001c0001t0002g0059 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.3782-18624A>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27769720 | ||||||
chr22:27769762
|
C | G | 264 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0055others(261): Show | 268 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(265): Show |
intron_variant | MODIFIER | c.3782-18666G>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27769762 | ||||||
chr22:27769790
|
G | A | 3 | a0001c0001t0023g0019a0001c0001t0069g0373a0001c0013t0001g0047 | 3 | HG02055.hp2 HG02896.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.3782-18694C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27769790 | ||||||
chr22:27769819
|
G | A | 143 | a0001c0001t0001g0003a0001c0001t0001g0078a0001c0001t0001g0107others(140): Show | 145 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(142): Show |
intron_variant | MODIFIER | c.3782-18723C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27769819 | ||||||
chr22:27769863
|
AT | A | 131 | a0001c0001t0001g0001a0001c0001t0001g0055a0001c0001t0001g0071others(128): Show | 133 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.3782-18768delA | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27769863 | ||||||
chr22:27770032
|
T | C | 1 | a0003c0004t0016g0248 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3782-18936A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27770032 | ||||||
chr22:27770095
|
T | C | 1 | a0001c0001t0008g0228 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.3782-18999A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27770095 | ||||||
chr22:27770105
|
C | T | 1 | a0001c0001t0002g0236 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3782-19009G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27770105 | ||||||
chr22:27770152
|
C | T | 1 | a0001c0005t0002g0054 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3782-19056G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27770152 | ||||||
chr22:27770296
|
C | T | 2 | a0001c0005t0043g0037a0002c0003t0014g0021 | 2 | NA19030.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3782-19200G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27770296 | ||||||
chr22:27770315
|
G | A | 15 | a0001c0001t0001g0078a0001c0001t0002g0212a0001c0001t0003g0306others(12): Show | 15 | HG00673.hp1 HG00673.hp2 HG02015.hp1 others(12): Show |
intron_variant | MODIFIER | c.3782-19219C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27770315 | ||||||
chr22:27770414
|
C | G | 39 | a0001c0001t0001g0004a0001c0001t0001g0061a0001c0001t0001g0064others(36): Show | 42 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(39): Show |
intron_variant | MODIFIER | c.3782-19318G>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27770414 | ||||||
chr22:27770447
|
AATCATGT others(2): Show |
A | 142 | a0001c0001t0001g0003a0001c0001t0001g0078a0001c0001t0001g0107others(139): Show | 144 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.3782-19360_3782-19 others(15): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27770447 | ||||||
chr22:27770458
|
T | C | 2 | a0001c0009t0021g0006a0003c0004t0016g0248 | 3 | HG02451.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3782-19362A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27770458 | ||||||
chr22:27770482
|
C | A | 24 | a0001c0001t0001g0001a0001c0001t0001g0055a0001c0001t0001g0100others(21): Show | 25 | HG00099.hp2 HG00323.hp1 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.3782-19386G>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27770482 | ||||||
chr22:27770518
|
C | T | 1 | a0001c0001t0002g0090 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.3782-19422G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27770518 | ||||||
chr22:27770575
|
C | T | 1 | a0001c0001t0001g0151 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.3782-19479G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27770575 | ||||||
chr22:27770662
|
TTTATTTT others(61): Show |
T | 26 | a0001c0001t0001g0078a0001c0001t0001g0124a0001c0001t0002g0212others(23): Show | 27 | HG00673.hp1 HG00673.hp2 HG02015.hp1 others(24): Show |
intron_variant | MODIFIER | c.3782-19634_3782-19 others(74): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27770662 | ||||||
chr22:27770872
|
T | C | 19 | a0001c0001t0001g0157a0001c0001t0002g0059a0001c0001t0002g0066others(16): Show | 19 | HG00323.hp2 HG00609.hp1 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.3782-19776A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27770872 | ||||||
chr22:27770935
|
C | T | 8 | a0001c0001t0001g0078a0001c0001t0002g0212a0001c0001t0003g0306others(5): Show | 8 | HG00673.hp2 HG02015.hp1 NA18941.hp2 others(5): Show |
intron_variant | MODIFIER | c.3782-19839G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27770935 | ||||||
chr22:27771096
|
G | A | 1 | a0001c0001t0062g0063 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3782-20000C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27771096 | ||||||
chr22:27771136
|
A | G | 4 | a0001c0001t0001g0134a0001c0005t0009g0016a0001c0010t0024g0013others(1): Show | 4 | HG01496.hp1 HG02280.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.3782-20040T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27771136 | ||||||
chr22:27771163
|
A | G | 1 | a0001c0001t0002g0214 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3782-20067T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27771163 | ||||||
chr22:27771219
|
C | CTT | 22 | a0001c0001t0001g0078a0001c0001t0001g0124a0001c0001t0002g0212others(19): Show | 24 | HG00673.hp2 HG01243.hp2 HG02015.hp1 others(21): Show |
intron_variant | MODIFIER | c.3782-20125_3782-20 others(8): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27771219 | ||||||
chr22:27771219
|
C | CTTT | 26 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0152others(23): Show | 26 | HG01192.hp2 HG02055.hp1 HG02451.hp1 others(23): Show |
intron_variant | MODIFIER | c.3782-20126_3782-20 others(9): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27771219 | ||||||
chr22:27771219
|
CT | C | 144 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0064others(141): Show | 149 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.3782-20124delA | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27771219 | ||||||
chr22:27771219
|
CTT | C | 13 | a0001c0001t0001g0210a0001c0001t0002g0177a0001c0001t0002g0192others(10): Show | 13 | HG00558.hp2 HG01070.hp2 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.3782-20125_3782-20 others(8): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27771219 | ||||||
chr22:27771219
|
CTTTT | C | 41 | a0001c0001t0001g0093a0001c0001t0001g0119a0001c0001t0001g0144others(38): Show | 41 | HG00140.hp2 HG00558.hp1 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.3782-20127_3782-20 others(10): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27771219 | ||||||
chr22:27771219
|
CTTTTTTT others(5): Show |
C | 3 | a0001c0001t0002g0223a0001c0001t0025g0041a0002c0003t0041g0027 | 3 | HG01891.hp2 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.3782-20135_3782-20 others(18): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27771219 | ||||||
chr22:27771297
|
T | C | 1 | a0001c0001t0006g0129 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3782-20201A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27771297 | ||||||
chr22:27771433
|
C | T | 1 | a0002c0002t0007g0258 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.3782-20337G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27771433 | ||||||
chr22:27771535
|
T | G | 18 | a0001c0001t0001g0124a0001c0001t0001g0229a0001c0001t0002g0125others(15): Show | 19 | HG01243.hp2 HG02257.hp2 HG02809.hp1 others(16): Show |
intron_variant | MODIFIER | c.3782-20439A>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27771535 | ||||||
chr22:27771647
|
C | T | 1 | a0001c0001t0003g0348 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.3782-20551G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27771647 | ||||||
chr22:27771687
|
G | A | 1 | a0002c0002t0003g0363 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.3782-20591C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27771687 | ||||||
chr22:27771920
|
T | A | 1 | a0001c0001t0001g0128 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.3782-20824A>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27771920 | ||||||
chr22:27772071
|
G | A | 1 | a0001c0001t0023g0019 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3782-20975C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27772071 | ||||||
chr22:27772110
|
C | A | 1 | a0001c0010t0024g0013 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3782-21014G>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27772110 | ||||||
chr22:27772264
|
C | T | 91 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0071others(88): Show | 94 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.3782-21168G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27772264 | ||||||
chr22:27772345
|
C | T | 1 | a0002c0003t0014g0029 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3782-21249G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27772345 | ||||||
chr22:27772346
|
G | A | 1 | a0001c0001t0066g0307 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.3782-21250C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27772346 | ||||||
chr22:27772359
|
A | G | 75 | a0001c0001t0001g0055a0001c0001t0001g0061a0001c0001t0001g0065others(72): Show | 78 | HG00099.hp1 HG00639.hp2 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.3782-21263T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27772359 | ||||||
chr22:27772386
|
A | C | 2 | a0001c0001t0002g0232a0001c0021t0007g0250 | 2 | HG01891.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3782-21290T>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27772386 | ||||||
chr22:27772495
|
G | C | 79 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0071others(76): Show | 82 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.3782-21399C>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27772495 | ||||||
chr22:27772503
|
C | G | 4 | a0001c0001t0002g0070a0001c0001t0002g0175a0001c0001t0023g0019others(1): Show | 4 | HG01192.hp2 HG02630.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.3782-21407G>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27772503 | ||||||
chr22:27772597
|
C | T | 66 | a0001c0001t0001g0001a0001c0001t0001g0079a0001c0001t0001g0081others(63): Show | 67 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.3782-21501G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27772597 | ||||||
chr22:27772691
|
C | T | 1 | a0001c0001t0004g0321 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.3782-21595G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27772691 | ||||||
chr22:27772796
|
T | C | 6 | a0001c0001t0001g0093a0001c0001t0002g0087a0001c0001t0002g0088others(3): Show | 6 | HG00140.hp1 HG01167.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.3782-21700A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27772796 | ||||||
chr22:27772817
|
T | C | 2 | a0001c0005t0049g0052a0001c0013t0001g0047 | 2 | HG02451.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.3782-21721A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27772817 | ||||||
chr22:27772852
|
C | CCAT | 20 | a0001c0001t0001g0093a0001c0001t0001g0097a0001c0001t0002g0062others(17): Show | 20 | HG00673.hp2 HG00735.hp2 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.3782-21759_3782-21 others(9): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27772852 | ||||||
chr22:27772852
|
C | CCATCAT | 34 | a0001c0001t0001g0094a0001c0001t0001g0098a0001c0001t0001g0124others(31): Show | 35 | HG01243.hp1 HG01496.hp2 HG01891.hp2 others(32): Show |
intron_variant | MODIFIER | c.3782-21762_3782-21 others(12): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27772852 | ||||||
chr22:27772852
|
C | CCATCATC others(2): Show |
3 | a0001c0001t0069g0373a0001c0009t0021g0006a0003c0004t0016g0248 | 4 | HG02055.hp2 HG02451.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.3782-21765_3782-21 others(15): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27772852 | ||||||
chr22:27772880
|
CATCATA | C | 77 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0071others(74): Show | 80 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.3782-21790_3782-21 others(12): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27772880 | ||||||
chr22:27772886
|
A | C | 5 | a0001c0001t0001g0137a0001c0001t0002g0232a0001c0005t0049g0052others(2): Show | 5 | HG01123.hp1 HG01891.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.3782-21790T>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27772886 | ||||||
chr22:27772959
|
G | C | 1 | a0001c0001t0003g0319 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.3782-21863C>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27772959 | ||||||
chr22:27772959
|
G | T | 1 | a0001c0001t0008g0196 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.3782-21863C>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27772959 | ||||||
chr22:27773072
|
C | G | 2 | a0001c0001t0016g0110a0001c0013t0048g0046 | 2 | HG03209.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.3782-21976G>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27773072 | ||||||
chr22:27773089
|
C | T | 2 | a0001c0014t0018g0374a0003c0004t0001g0247 | 2 | HG02055.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.3782-21993G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27773089 | ||||||
chr22:27773099
|
A | T | 1 | a0002c0003t0009g0022 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3782-22003T>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27773099 | ||||||
chr22:27773149
|
C | T | 1 | a0002c0002t0006g0266 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.3782-22053G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27773149 | ||||||
chr22:27773318
|
A | G | 3 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132 | 3 | NA18992.hp2 NA19011.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.3782-22222T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27773318 | ||||||
chr22:27773469
|
A | G | 2 | a0001c0001t0002g0126a0001c0001t0075g0384 | 2 | HG03041.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.3782-22373T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27773469 | ||||||
chr22:27773501
|
AC | A | 7 | a0001c0001t0002g0116a0001c0001t0076g0386a0001c0005t0049g0052others(4): Show | 7 | HG01496.hp2 HG02451.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.3782-22406delG | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27773501 | ||||||
chr22:27773511
|
C | T | 151 | a0001c0001t0001g0061a0001c0001t0001g0064a0001c0001t0001g0065others(148): Show | 155 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.3782-22415G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27773511 | ||||||
chr22:27773533
|
C | A | 326 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(323): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.3782-22437G>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27773533 | ||||||
chr22:27773553
|
G | A | 1 | a0001c0001t0010g0328 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.3782-22457C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27773553 | ||||||
chr22:27773589
|
T | A | 1 | a0001c0001t0001g0111 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.3782-22493A>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27773589 | ||||||
chr22:27773804
|
G | A | 5 | a0001c0001t0002g0125a0001c0001t0002g0214a0001c0001t0044g0040others(2): Show | 5 | HG02109.hp2 HG02809.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.3782-22708C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27773804 | ||||||
chr22:27773907
|
G | C | 2 | a0001c0009t0021g0006a0003c0004t0016g0248 | 3 | HG02451.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3782-22811C>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27773907 | ||||||
chr22:27773961
|
T | G | 82 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0071others(79): Show | 85 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.3781+22802A>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27773961 | ||||||
chr22:27774043
|
C | A | 92 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0071others(89): Show | 95 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.3781+22720G>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27774043 | ||||||
chr22:27774046
|
C | A | 1 | a0001c0001t0001g0139 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.3781+22717G>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27774046 | ||||||
chr22:27774156
|
G | C | 1 | a0001c0001t0054g0150 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3781+22607C>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27774156 | ||||||
chr22:27774158
|
C | A | 1 | a0001c0001t0054g0150 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3781+22605G>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27774158 | ||||||
chr22:27774161
|
A | C | 1 | a0001c0001t0054g0150 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3781+22602T>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27774161 | ||||||
chr22:27774163
|
G | T | 1 | a0001c0001t0054g0150 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3781+22600C>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27774163 | ||||||
chr22:27774166
|
C | T | 1 | a0001c0001t0054g0150 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3781+22597G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27774166 | ||||||
chr22:27774167
|
T | G | 1 | a0001c0001t0054g0150 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3781+22596A>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27774167 | ||||||
chr22:27774168
|
C | A | 1 | a0001c0001t0054g0150 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3781+22595G>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27774168 | ||||||
chr22:27774170
|
C | G | 1 | a0001c0001t0054g0150 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3781+22593G>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27774170 | ||||||
chr22:27774172
|
G | T | 1 | a0001c0001t0054g0150 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3781+22591C>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27774172 | ||||||
chr22:27774178
|
A | C | 97 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0071others(94): Show | 100 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.3781+22585T>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27774178 | ||||||
chr22:27774229
|
C | T | 144 | a0001c0001t0001g0074a0001c0001t0001g0078a0001c0001t0001g0093others(141): Show | 146 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.3781+22534G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27774229 | ||||||
chr22:27774292
|
C | T | 43 | a0001c0001t0001g0076a0001c0001t0001g0082a0001c0001t0001g0146others(40): Show | 43 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.3781+22471G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27774292 | ||||||
chr22:27774505
|
T | C | 2 | a0001c0001t0002g0232a0001c0021t0007g0250 | 2 | HG01891.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3781+22258A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27774505 | ||||||
chr22:27774606
|
A | G | 1 | a0001c0001t0002g0176 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3781+22157T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27774606 | ||||||
chr22:27774623
|
A | G | 1 | a0001c0005t0016g0053 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3781+22140T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27774623 | ||||||
chr22:27774686
|
C | A | 1 | a0002c0002t0023g0035 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3781+22077G>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27774686 | ||||||
chr22:27774702
|
G | A | 76 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0071others(73): Show | 79 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.3781+22061C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27774702 | ||||||
chr22:27774708
|
G | A | 1 | a0001c0001t0002g0114 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.3781+22055C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27774708 | ||||||
chr22:27774726
|
G | A | 1 | a0001c0001t0003g0339 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.3781+22037C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27774726 | ||||||
chr22:27774726
|
G | C | 2 | a0001c0001t0002g0232a0001c0021t0007g0250 | 2 | HG01891.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3781+22037C>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27774726 | ||||||
chr22:27774735
|
A | T | 106 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0074others(103): Show | 108 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.3781+22028T>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27774735 | ||||||
chr22:27774802
|
G | A | 1 | a0002c0002t0007g0256 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.3781+21961C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27774802 | ||||||
chr22:27774834
|
T | C | 3 | a0001c0001t0004g0334a0001c0001t0004g0335a0001c0001t0025g0039 | 3 | HG01346.hp1 HG01358.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.3781+21929A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27774834 | ||||||
chr22:27774858
|
T | C | 6 | a0001c0001t0002g0116a0001c0001t0002g0175a0001c0001t0076g0386others(3): Show | 6 | HG01496.hp2 HG02630.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.3781+21905A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27774858 | ||||||
chr22:27774904
|
C | T | 2 | a0001c0001t0002g0232a0001c0021t0007g0250 | 2 | HG01891.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3781+21859G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27774904 | ||||||
chr22:27775056
|
C | T | 6 | a0001c0001t0002g0116a0001c0001t0002g0175a0001c0001t0076g0386others(3): Show | 6 | HG01496.hp2 HG02630.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.3781+21707G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27775056 | ||||||
chr22:27775325
|
C | T | 2 | a0001c0001t0006g0215a0001c0001t0012g0298 | 2 | NA18970.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.3781+21438G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27775325 | ||||||
chr22:27775399
|
G | A | 1 | a0001c0001t0026g0043 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.3781+21364C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27775399 | ||||||
chr22:27775522
|
C | T | 32 | a0001c0001t0001g0128a0001c0001t0001g0211a0001c0001t0002g0070others(29): Show | 32 | HG00438.hp2 HG01099.hp1 HG01192.hp2 others(29): Show |
intron_variant | MODIFIER | c.3781+21241G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27775522 | ||||||
chr22:27775948
|
G | GA | 93 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0071others(90): Show | 97 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.3781+20814dupT | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27775948 | ||||||
chr22:27776056
|
C | G | 3 | a0001c0001t0003g0300a0001c0001t0003g0338a0001c0001t0013g0299 | 3 | HG02080.hp1 NA18955.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.3781+20707G>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27776056 | ||||||
chr22:27776102
|
G | A | 7 | a0001c0001t0001g0134a0001c0001t0006g0218a0001c0001t0023g0019others(4): Show | 7 | HG01243.hp2 HG02717.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.3781+20661C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27776102 | ||||||
chr22:27776248
|
T | C | 3 | a0001c0001t0002g0087a0001c0001t0002g0088a0001c0001t0002g0089 | 3 | HG01256.hp2 HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.3781+20515A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27776248 | ||||||
chr22:27776251
|
G | A | 1 | a0002c0002t0002g0263 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.3781+20512C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27776251 | ||||||
chr22:27776300
|
G | A | 2 | a0001c0001t0006g0218a0001c0001t0010g0308 | 2 | HG02895.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.3781+20463C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27776300 | ||||||
chr22:27776473
|
T | C | 1 | a0001c0001t0001g0193 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3781+20290A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27776473 | ||||||
chr22:27776543
|
G | A | 12 | a0001c0001t0001g0124a0001c0001t0002g0213a0001c0001t0053g0123others(9): Show | 13 | HG02055.hp2 HG02717.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.3781+20220C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27776543 | ||||||
chr22:27776556
|
C | A | 1 | a0001c0001t0001g0094 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.3781+20207G>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27776556 | ||||||
chr22:27776589
|
T | G | 299 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0055others(296): Show | 305 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(302): Show |
intron_variant | MODIFIER | c.3781+20174A>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27776589 | ||||||
chr22:27776697
|
C | T | 1 | a0001c0016t0003g0280 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.3781+20066G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27776697 | ||||||
chr22:27776738
|
C | T | 1 | a0001c0001t0001g0227 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.3781+20025G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27776738 | ||||||
chr22:27777015
|
G | A | 2 | a0001c0001t0002g0113a0001c0001t0007g0115 | 2 | NA18974.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.3781+19748C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27777015 | ||||||
chr22:27777026
|
G | A | 24 | a0001c0001t0001g0128a0001c0001t0001g0211a0001c0001t0002g0070others(21): Show | 24 | HG00438.hp2 HG01099.hp1 HG01192.hp2 others(21): Show |
intron_variant | MODIFIER | c.3781+19737C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27777026 | ||||||
chr22:27777042
|
G | A | 203 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0071others(200): Show | 207 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.3781+19721C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27777042 | ||||||
chr22:27777059
|
C | T | 4 | a0001c0001t0002g0236a0001c0001t0009g0020a0001c0001t0016g0224others(1): Show | 4 | HG02145.hp1 HG02622.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.3781+19704G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27777059 | ||||||
chr22:27777092
|
C | T | 1 | a0005c0011t0019g0015 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3781+19671G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27777092 | ||||||
chr22:27777159
|
C | T | 1 | a0001c0014t0018g0375 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3781+19604G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27777159 | ||||||
chr22:27777163
|
A | T | 3 | a0001c0001t0007g0173a0001c0001t0012g0354a0001c0001t0050g0174 | 3 | HG00609.hp2 NA18612.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.3781+19600T>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27777163 | ||||||
chr22:27777208
|
T | C | 7 | a0001c0001t0001g0134a0001c0001t0006g0218a0001c0001t0023g0019others(4): Show | 7 | HG01243.hp2 HG02717.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.3781+19555A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27777208 | ||||||
chr22:27777241
|
G | A | 1 | a0001c0001t0001g0227 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.3781+19522C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27777241 | ||||||
chr22:27777440
|
G | A | 1 | a0001c0001t0057g0237 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3781+19323C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27777440 | ||||||
chr22:27777533
|
TA | T | 199 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0072others(196): Show | 203 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.3781+19229delT | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27777533 | ||||||
chr22:27777533
|
TAA | T | 10 | a0001c0001t0001g0071a0001c0001t0001g0134a0001c0001t0001g0155others(7): Show | 10 | HG00639.hp1 HG01257.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.3781+19228_3781+19 others(8): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27777533 | ||||||
chr22:27777547
|
A | AG | 84 | a0001c0001t0001g0055a0001c0001t0001g0061a0001c0001t0001g0065others(81): Show | 86 | HG00099.hp1 HG00423.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.3781+19215_3781+19 others(7): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27777547 | ||||||
chr22:27777557
|
GA | G | 84 | a0001c0001t0001g0055a0001c0001t0001g0061a0001c0001t0001g0065others(81): Show | 86 | HG00099.hp1 HG00423.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.3781+19205delT | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27777557 | ||||||
chr22:27777559
|
A | G | 1 | a0001c0001t0045g0042 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3781+19204T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27777559 | ||||||
chr22:27777582
|
A | G | 173 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0055others(170): Show | 178 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.3781+19181T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27777582 | ||||||
chr22:27777656
|
C | G | 1 | a0001c0001t0058g0233 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.3781+19107G>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27777656 | ||||||
chr22:27777686
|
G | A | 1 | a0001c0001t0008g0067 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.3781+19077C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27777686 | ||||||
chr22:27777702
|
T | TAC | 256 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0055others(253): Show | 261 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.3781+19059_3781+19 others(8): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27777702 | ||||||
chr22:27777714
|
C | G | 1 | a0002c0003t0009g0031 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3781+19049G>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27777714 | ||||||
chr22:27777777
|
G | A | 9 | a0001c0001t0001g0124a0001c0001t0002g0213a0001c0001t0053g0123others(6): Show | 10 | HG02055.hp2 HG02717.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.3781+18986C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27777777 | ||||||
chr22:27777877
|
C | CA | 22 | a0001c0001t0001g0124a0001c0001t0002g0213a0001c0001t0002g0223others(19): Show | 24 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.3781+18885dupT | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27777877 | ||||||
chr22:27777910
|
T | C | 294 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0055others(291): Show | 300 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(297): Show |
intron_variant | MODIFIER | c.3781+18853A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27777910 | ||||||
chr22:27777911
|
C | T | 5 | a0001c0001t0002g0057a0001c0001t0002g0206a0001c0001t0068g0331others(2): Show | 5 | HG02559.hp2 HG02976.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.3781+18852G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27777911 | ||||||
chr22:27777969
|
G | A | 1 | a0005c0011t0019g0015 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3781+18794C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27777969 | ||||||
chr22:27778122
|
G | A | 1 | a0001c0001t0057g0237 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3781+18641C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27778122 | ||||||
chr22:27778193
|
G | T | 1 | a0001c0001t0074g0385 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3781+18570C>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27778193 | ||||||
chr22:27778304
|
G | A | 1 | a0001c0001t0003g0290 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.3781+18459C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27778304 | ||||||
chr22:27778352
|
C | T | 1 | a0001c0001t0001g0055 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.3781+18411G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27778352 | ||||||
chr22:27778432
|
C | G | 1 | a0003c0004t0001g0247 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3781+18331G>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27778432 | ||||||
chr22:27778433
|
G | A | 1 | a0001c0005t0016g0053 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3781+18330C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27778433 | ||||||
chr22:27778609
|
G | A | 42 | a0001c0001t0001g0055a0001c0001t0001g0078a0001c0001t0001g0083others(39): Show | 42 | HG00621.hp1 HG00741.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.3781+18154C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27778609 | ||||||
chr22:27778644
|
C | T | 50 | a0001c0001t0001g0055a0001c0001t0001g0078a0001c0001t0001g0083others(47): Show | 51 | HG00621.hp1 HG00741.hp1 HG01243.hp1 others(48): Show |
intron_variant | MODIFIER | c.3781+18119G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27778644 | ||||||
chr22:27778702
|
C | T | 2 | a0001c0001t0002g0232a0001c0021t0007g0250 | 2 | HG01891.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3781+18061G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27778702 | ||||||
chr22:27778710
|
C | G | 1 | a0001c0001t0005g0085 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.3781+18053G>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27778710 | ||||||
chr22:27778836
|
G | A | 1 | a0002c0003t0009g0031 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3781+17927C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27778836 | ||||||
chr22:27778961
|
G | A | 4 | a0001c0001t0002g0062a0001c0008t0018g0379a0002c0002t0004g0367others(1): Show | 4 | HG00735.hp2 HG01261.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.3781+17802C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27778961 | ||||||
chr22:27778981
|
G | C | 302 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(299): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.3781+17782C>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27778981 | ||||||
chr22:27779007
|
C | G | 1 | a0001c0001t0002g0223 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3781+17756G>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27779007 | ||||||
chr22:27779174
|
C | T | 135 | a0001c0001t0001g0055a0001c0001t0001g0061a0001c0001t0001g0065others(132): Show | 137 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.3781+17589G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27779174 | ||||||
chr22:27779244
|
T | C | 1 | a0001c0001t0001g0100 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3781+17519A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27779244 | ||||||
chr22:27779402
|
G | A | 2 | a0001c0001t0002g0057a0005c0011t0019g0015 | 2 | HG02976.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.3781+17361C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27779402 | ||||||
chr22:27779529
|
A | G | 1 | a0001c0001t0037g0009 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.3781+17234T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27779529 | ||||||
chr22:27779753
|
G | A | 175 | a0001c0001t0001g0055a0001c0001t0001g0061a0001c0001t0001g0065others(172): Show | 177 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.3781+17010C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27779753 | ||||||
chr22:27779754
|
C | G | 1 | a0001c0001t0057g0237 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3781+17009G>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27779754 | ||||||
chr22:27779783
|
C | T | 1 | a0002c0003t0019g0032 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3781+16980G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27779783 | ||||||
chr22:27780170
|
G | A | 12 | a0001c0001t0001g0097a0001c0001t0002g0176a0001c0001t0002g0212others(9): Show | 12 | HG00673.hp2 HG02080.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.3781+16593C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27780170 | ||||||
chr22:27780422
|
T | TCCAGGGT others(2): Show |
3 | a0001c0001t0001g0235a0001c0001t0002g0126a0001c0001t0075g0384 | 3 | HG03041.hp2 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.3781+16332_3781+16 others(15): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27780422 | ||||||
chr22:27780518
|
A | G | 1 | a0001c0001t0001g0205 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.3781+16245T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27780518 | ||||||
chr22:27780733
|
C | T | 1 | a0001c0001t0008g0199 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.3781+16030G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27780733 | ||||||
chr22:27780789
|
A | G | 32 | a0001c0001t0001g0229a0001c0001t0001g0235a0001c0001t0002g0062others(29): Show | 32 | HG00735.hp2 HG01243.hp1 HG01261.hp2 others(29): Show |
intron_variant | MODIFIER | c.3781+15974T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27780789 | ||||||
chr22:27780842
|
G | A | 4 | a0001c0001t0001g0076a0001c0001t0001g0082a0001c0001t0052g0080others(1): Show | 4 | NA18941.hp1 NA18949.hp1 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.3781+15921C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27780842 | ||||||
chr22:27780909
|
CTA | C | 26 | a0001c0001t0001g0229a0001c0001t0002g0062a0001c0001t0002g0116others(23): Show | 26 | HG00735.hp2 HG01243.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.3781+15852_3781+15 others(8): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27780909 | ||||||
chr22:27780934
|
A | AT | 34 | a0001c0001t0001g0229a0001c0001t0002g0062a0001c0001t0002g0116others(31): Show | 34 | HG00735.hp2 HG01243.hp1 HG01261.hp2 others(31): Show |
intron_variant | MODIFIER | c.3781+15828dupA | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27780934 | ||||||
chr22:27780957
|
G | C | 5 | a0001c0001t0002g0058a0002c0003t0015g0023a0002c0003t0015g0024others(2): Show | 5 | HG02145.hp2 HG02257.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.3781+15806C>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27780957 | ||||||
chr22:27781297
|
A | G | 1 | a0001c0005t0002g0054 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3781+15466T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27781297 | ||||||
chr22:27781366
|
C | T | 1 | a0001c0001t0028g0234 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3781+15397G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27781366 | ||||||
chr22:27781515
|
G | A | 4 | a0001c0001t0002g0062a0001c0008t0018g0379a0002c0002t0004g0367others(1): Show | 4 | HG00735.hp2 HG01261.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.3781+15248C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27781515 | ||||||
chr22:27781707
|
G | A | 2 | a0001c0001t0002g0176a0001c0001t0076g0386 | 2 | HG02486.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.3781+15056C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27781707 | ||||||
chr22:27781900
|
G | A | 3 | a0001c0001t0025g0041a0001c0010t0014g0011a0002c0003t0014g0021 | 3 | HG02886.hp2 HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.3781+14863C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27781900 | ||||||
chr22:27782022
|
G | A | 37 | a0001c0001t0001g0055a0001c0001t0001g0078a0001c0001t0001g0083others(34): Show | 37 | HG00408.hp2 HG00621.hp1 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.3781+14741C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27782022 | ||||||
chr22:27782117
|
C | T | 1 | a0001c0001t0002g0108 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.3781+14646G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27782117 | ||||||
chr22:27782213
|
C | T | 54 | a0001c0001t0001g0055a0001c0001t0001g0078a0001c0001t0001g0083others(51): Show | 54 | HG00408.hp2 HG00423.hp2 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.3781+14550G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27782213 | ||||||
chr22:27782214
|
G | A | 1 | a0002c0003t0014g0034 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3781+14549C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27782214 | ||||||
chr22:27782329
|
G | A | 2 | a0001c0001t0004g0336a0001c0001t0012g0337 | 2 | NA18950.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.3781+14434C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27782329 | ||||||
chr22:27782437
|
A | T | 31 | a0001c0001t0001g0229a0001c0001t0002g0062a0001c0001t0002g0116others(28): Show | 31 | HG00735.hp2 HG01243.hp1 HG01261.hp2 others(28): Show |
intron_variant | MODIFIER | c.3781+14326T>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27782437 | ||||||
chr22:27782526
|
C | T | 2 | a0001c0001t0010g0308a0002c0002t0004g0370 | 2 | HG01515.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.3781+14237G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27782526 | ||||||
chr22:27782602
|
T | C | 34 | a0001c0001t0001g0229a0001c0001t0001g0235a0001c0001t0002g0062others(31): Show | 34 | HG00735.hp2 HG01243.hp1 HG01261.hp2 others(31): Show |
intron_variant | MODIFIER | c.3781+14161A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27782602 | ||||||
chr22:27782637
|
T | A | 2 | a0001c0001t0002g0176a0001c0001t0076g0386 | 2 | HG02486.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.3781+14126A>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27782637 | ||||||
chr22:27782663
|
T | C | 14 | a0001c0001t0001g0229a0001c0001t0002g0125a0001c0001t0002g0214others(11): Show | 14 | HG01884.hp1 HG02055.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.3781+14100A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27782663 | ||||||
chr22:27782706
|
G | C | 1 | a0001c0001t0001g0061 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.3781+14057C>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27782706 | ||||||
chr22:27782942
|
T | C | 1 | a0001c0001t0057g0237 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3781+13821A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27782942 | ||||||
chr22:27782960
|
G | A | 21 | a0001c0001t0001g0134a0001c0001t0001g0235a0001c0001t0002g0062others(18): Show | 21 | HG00735.hp2 HG01243.hp1 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.3781+13803C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27782960 | ||||||
chr22:27782973
|
C | T | 1 | a0001c0001t0057g0237 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3781+13790G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27782973 | ||||||
chr22:27782979
|
G | C | 1 | a0001c0001t0001g0093 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3781+13784C>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27782979 | ||||||
chr22:27783133
|
C | CT | 46 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0124others(43): Show | 46 | HG00423.hp1 HG00438.hp2 HG01099.hp1 others(43): Show |
intron_variant | MODIFIER | c.3781+13629dupA | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27783133 | ||||||
chr22:27783133
|
CT | C | 11 | a0001c0001t0001g0111a0001c0001t0001g0208a0001c0001t0002g0116others(8): Show | 11 | HG01243.hp1 HG01496.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.3781+13629delA | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27783133 | ||||||
chr22:27783247
|
G | A | 56 | a0001c0001t0001g0055a0001c0001t0001g0078a0001c0001t0001g0083others(53): Show | 56 | HG00408.hp2 HG00423.hp2 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.3781+13516C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27783247 | ||||||
chr22:27783296
|
T | G | 1 | a0001c0001t0004g0353 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.3781+13467A>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27783296 | ||||||
chr22:27783343
|
G | A | 1 | a0001c0009t0021g0006 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3781+13420C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27783343 | ||||||
chr22:27783592
|
C | A | 8 | a0001c0001t0002g0116a0001c0001t0002g0175a0001c0005t0002g0048others(5): Show | 8 | HG01243.hp1 HG01496.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.3781+13171G>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27783592 | ||||||
chr22:27783835
|
T | C | 311 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(308): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.3781+12928A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27783835 | ||||||
chr22:27783852
|
A | AGTCCGAA others(1): Show |
3 | a0001c0001t0001g0180a0001c0001t0002g0059a0001c0001t0003g0319 | 3 | HG03654.hp1 HG03927.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.3781+12903_3781+12 others(14): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27783852 | ||||||
chr22:27783868
|
C | T | 26 | a0001c0001t0001g0074a0001c0001t0001g0235a0001c0001t0002g0147others(23): Show | 26 | HG00609.hp2 HG01243.hp2 HG01993.hp1 others(23): Show |
intron_variant | MODIFIER | c.3781+12895G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27783868 | ||||||
chr22:27783879
|
C | T | 2 | a0001c0001t0045g0042a0001c0001t0069g0373 | 2 | HG02055.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.3781+12884G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27783879 | ||||||
chr22:27783961
|
C | T | 3 | a0001c0001t0016g0110a0002c0003t0015g0025a0002c0003t0015g0026 | 3 | HG01884.hp1 HG02572.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.3781+12802G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27783961 | ||||||
chr22:27784323
|
C | A | 2 | a0001c0001t0001g0166a0001c0001t0001g0167 | 2 | HG03017.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.3781+12440G>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27784323 | ||||||
chr22:27784446
|
A | G | 1 | a0001c0001t0002g0070 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.3781+12317T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27784446 | ||||||
chr22:27784527
|
CTAAAGTT | C | 19 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0136others(16): Show | 20 | HG00099.hp1 HG00642.hp1 HG01099.hp2 others(17): Show |
intron_variant | MODIFIER | c.3781+12229_3781+12 others(13): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27784527 | ||||||
chr22:27784561
|
G | C | 6 | a0001c0001t0002g0086a0001c0001t0002g0130a0001c0001t0002g0131others(3): Show | 6 | NA18966.hp1 NA18992.hp2 NA19011.hp2 others(3): Show |
intron_variant | MODIFIER | c.3781+12202C>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27784561 | ||||||
chr22:27784690
|
A | G | 2 | a0001c0001t0002g0126a0001c0001t0075g0384 | 2 | HG03041.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.3781+12073T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27784690 | ||||||
chr22:27784720
|
G | A | 10 | a0001c0001t0002g0212a0001c0001t0003g0300a0001c0001t0003g0338others(7): Show | 10 | HG00621.hp1 HG00673.hp2 HG02080.hp1 others(7): Show |
intron_variant | MODIFIER | c.3781+12043C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27784720 | ||||||
chr22:27784869
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.3781+11894G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27784869 | ||||||
chr22:27785024
|
G | T | 2 | a0001c0001t0002g0070a0002c0002t0023g0035 | 2 | HG01192.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.3781+11739C>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27785024 | ||||||
chr22:27785056
|
C | CCA | 36 | a0001c0001t0001g0064a0001c0001t0001g0078a0001c0001t0002g0062others(33): Show | 36 | HG00673.hp2 HG00735.hp2 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.3781+11705_3781+11 others(8): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27785056 | ||||||
chr22:27785056
|
C | CCACA | 17 | a0001c0001t0001g0107a0001c0001t0001g0119a0001c0001t0001g0136others(14): Show | 17 | HG00558.hp1 HG00621.hp1 HG01496.hp1 others(14): Show |
intron_variant | MODIFIER | c.3781+11703_3781+11 others(10): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27785056 | ||||||
chr22:27785056
|
C | CCACACA | 24 | a0001c0001t0001g0137a0001c0001t0001g0183a0001c0001t0001g0220others(21): Show | 25 | HG00099.hp1 HG01081.hp2 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.3781+11701_3781+11 others(12): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27785056 | ||||||
chr22:27785056
|
C | CCACACAC others(1): Show |
17 | a0001c0001t0001g0074a0001c0001t0002g0177a0001c0001t0003g0342others(14): Show | 18 | HG00423.hp2 HG01515.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.3781+11699_3781+11 others(14): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27785056 | ||||||
chr22:27785056
|
C | CCACACAC others(3): Show |
21 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0139others(18): Show | 21 | HG00642.hp1 HG01175.hp1 HG01975.hp2 others(18): Show |
intron_variant | MODIFIER | c.3781+11697_3781+11 others(16): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27785056 | ||||||
chr22:27785056
|
C | CCACACAC others(5): Show |
3 | a0001c0001t0004g0356a0001c0001t0066g0307a0001c0012t0001g0278 | 3 | NA18959.hp1 NA19004.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.3781+11695_3781+11 others(18): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27785056 | ||||||
chr22:27785056
|
C | CCACACAC others(7): Show |
3 | a0001c0001t0003g0329a0001c0001t0004g0347a0001c0001t0026g0044 | 3 | HG02523.hp1 NA18947.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.3781+11693_3781+11 others(20): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27785056 | ||||||
chr22:27785056
|
CCA | C | 18 | a0001c0001t0001g0055a0001c0001t0001g0204a0001c0001t0002g0095others(15): Show | 18 | HG00741.hp2 HG01099.hp1 HG01123.hp2 others(15): Show |
intron_variant | MODIFIER | c.3781+11705_3781+11 others(8): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27785056 | ||||||
chr22:27785056
|
CCACA | C | 101 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0071others(98): Show | 105 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.3781+11703_3781+11 others(10): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27785056 | ||||||
chr22:27785056
|
CCACACA | C | 42 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0097others(39): Show | 42 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(39): Show |
intron_variant | MODIFIER | c.3781+11701_3781+11 others(12): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27785056 | ||||||
chr22:27785056
|
CCACACAC others(1): Show |
C | 7 | a0001c0001t0002g0086a0001c0001t0002g0116a0001c0001t0002g0130others(4): Show | 7 | HG03195.hp1 NA18966.hp1 NA18992.hp2 others(4): Show |
intron_variant | MODIFIER | c.3781+11699_3781+11 others(14): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27785056 | ||||||
chr22:27785056
|
CCACACAC others(9): Show |
C | 1 | a0002c0002t0023g0035 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3781+11691_3781+11 others(22): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27785056 | ||||||
chr22:27785101
|
T | G | 1 | a0001c0001t0001g0082 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.3781+11662A>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27785101 | ||||||
chr22:27785223
|
G | C | 2 | a0001c0001t0002g0070a0002c0002t0023g0035 | 2 | HG01192.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.3781+11540C>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27785223 | ||||||
chr22:27785225
|
C | T | 3 | a0001c0001t0002g0126a0001c0001t0075g0384a0001c0009t0021g0006 | 4 | HG02895.hp1 HG02897.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.3781+11538G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27785225 | ||||||
chr22:27785259
|
C | T | 1 | a0001c0001t0002g0185 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.3781+11504G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27785259 | ||||||
chr22:27785332
|
C | G | 1 | a0002c0003t0009g0031 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3781+11431G>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27785332 | ||||||
chr22:27785378
|
G | C | 1 | a0001c0001t0001g0207 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.3781+11385C>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27785378 | ||||||
chr22:27785406
|
T | C | 5 | a0001c0001t0016g0110a0001c0013t0001g0047a0001c0013t0048g0046others(2): Show | 5 | HG01884.hp1 HG02572.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.3781+11357A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27785406 | ||||||
chr22:27785411
|
C | T | 165 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(162): Show | 169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.3781+11352G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27785411 | ||||||
chr22:27785448
|
A | C | 312 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(309): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.3781+11315T>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27785448 | ||||||
chr22:27785510
|
C | T | 2 | a0001c0001t0002g0070a0003c0004t0002g0240 | 2 | HG01192.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.3781+11253G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27785510 | ||||||
chr22:27785746
|
G | GC | 61 | a0001c0001t0001g0055a0001c0001t0001g0076a0001c0001t0001g0081others(58): Show | 62 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.3781+11016dupG | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27785746 | ||||||
chr22:27785746
|
GC | G | 31 | a0001c0001t0001g0064a0001c0001t0001g0094a0001c0001t0001g0221others(28): Show | 31 | HG00741.hp2 HG01099.hp1 HG01123.hp2 others(28): Show |
intron_variant | MODIFIER | c.3781+11016delG | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27785746 | ||||||
chr22:27785746
|
GCC | G | 71 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0071others(68): Show | 74 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.3781+11015_3781+11 others(8): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27785746 | ||||||
chr22:27785753
|
C | CA | 58 | a0001c0001t0001g0001a0001c0001t0001g0093a0001c0001t0001g0097others(55): Show | 59 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(56): Show |
intron_variant | MODIFIER | c.3781+11009_3781+11 others(7): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27785753 | ||||||
chr22:27785790
|
A | G | 2 | a0001c0005t0002g0050a0001c0005t0028g0051 | 2 | HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.3781+10973T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27785790 | ||||||
chr22:27786304
|
C | T | 2 | a0001c0001t0002g0070a0003c0004t0002g0240 | 2 | HG01192.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.3781+10459G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27786304 | ||||||
chr22:27786430
|
A | AAC | 30 | a0001c0001t0001g0055a0001c0001t0001g0076a0001c0001t0001g0079others(27): Show | 30 | HG00408.hp2 HG01081.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.3781+10331_3781+10 others(8): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27786430 | ||||||
chr22:27786430
|
A | AACAC | 7 | a0001c0001t0001g0078a0001c0001t0001g0219a0001c0005t0002g0050others(4): Show | 7 | HG02300.hp1 HG02451.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.3781+10329_3781+10 others(10): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27786430 | ||||||
chr22:27786522
|
G | A | 10 | a0001c0001t0001g0074a0001c0001t0002g0068a0001c0001t0002g0177others(7): Show | 10 | HG01081.hp1 HG01993.hp1 HG02040.hp2 others(7): Show |
intron_variant | MODIFIER | c.3781+10241C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27786522 | ||||||
chr22:27786548
|
G | A | 1 | a0001c0001t0001g0004 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.3781+10215C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27786548 | ||||||
chr22:27786740
|
C | T | 2 | a0001c0001t0002g0070a0003c0004t0002g0240 | 2 | HG01192.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.3781+10023G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27786740 | ||||||
chr22:27786782
|
C | T | 1 | a0001c0001t0002g0178 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.3781+9981G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27786782 | ||||||
chr22:27786835
|
C | T | 2 | a0001c0001t0002g0070a0003c0004t0002g0240 | 2 | HG01192.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.3781+9928G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27786835 | ||||||
chr22:27786842
|
G | GCA | 100 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0071others(97): Show | 103 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.3781+9919_3781+992 others(6): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27786842 | ||||||
chr22:27786842
|
G | GCACA | 6 | a0001c0001t0003g0348a0001c0001t0004g0335a0001c0001t0005g0170others(3): Show | 6 | HG01346.hp1 HG02135.hp1 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.3781+9917_3781+992 others(8): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27786842 | ||||||
chr22:27786842
|
G | GCGCACAC others(5): Show |
2 | a0001c0001t0002g0070a0003c0004t0002g0240 | 2 | HG01192.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.3781+9920_3781+992 others(16): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27786842 | ||||||
chr22:27786842
|
GCA | G | 8 | a0001c0001t0001g0124a0001c0001t0001g0229a0001c0001t0002g0214others(5): Show | 8 | HG02109.hp2 HG02809.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.3781+9919_3781+992 others(6): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27786842 | ||||||
chr22:27786844
|
A | G | 1 | a0001c0001t0001g0235 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3781+9919T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27786844 | ||||||
chr22:27786895
|
G | A | 1 | a0001c0001t0057g0237 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3781+9868C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27786895 | ||||||
chr22:27786955
|
A | T | 1 | a0001c0001t0026g0044 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.3781+9808T>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27786955 | ||||||
chr22:27786982
|
T | G | 1 | a0001c0001t0003g0329 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.3781+9781A>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27786982 | ||||||
chr22:27787225
|
T | C | 1 | a0001c0001t0004g0347 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.3781+9538A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27787225 | ||||||
chr22:27787238
|
G | A | 2 | a0002c0003t0019g0032a0002c0003t0019g0033 | 2 | HG01496.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.3781+9525C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27787238 | ||||||
chr22:27787318
|
T | C | 2 | a0001c0001t0002g0070a0003c0004t0002g0240 | 2 | HG01192.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.3781+9445A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27787318 | ||||||
chr22:27787380
|
A | G | 1 | a0001c0001t0005g0077 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.3781+9383T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27787380 | ||||||
chr22:27787387
|
G | A | 1 | a0002c0003t0039g0028 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3781+9376C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27787387 | ||||||
chr22:27787665
|
G | T | 5 | a0001c0001t0045g0042a0001c0001t0059g0231a0001c0001t0069g0373others(2): Show | 5 | HG01516.hp2 HG02055.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.3781+9098C>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27787665 | ||||||
chr22:27787917
|
C | T | 1 | a0001c0001t0006g0216 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.3781+8846G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27787917 | ||||||
chr22:27787997
|
G | A | 1 | a0001c0001t0001g0128 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.3781+8766C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27787997 | ||||||
chr22:27788001
|
G | C | 5 | a0001c0005t0002g0050a0001c0005t0016g0053a0001c0005t0028g0051others(2): Show | 5 | HG02451.hp1 HG02451.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.3781+8762C>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27788001 | ||||||
chr22:27788147
|
G | A | 16 | a0001c0001t0001g0107a0001c0001t0001g0119a0001c0001t0002g0062others(13): Show | 16 | HG00438.hp1 HG00558.hp1 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.3781+8616C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27788147 | ||||||
chr22:27788189
|
G | A | 1 | a0001c0001t0001g0207 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.3781+8574C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27788189 | ||||||
chr22:27788301
|
A | G | 2 | a0001c0001t0045g0042a0001c0001t0069g0373 | 2 | HG02055.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.3781+8462T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27788301 | ||||||
chr22:27788309
|
T | C | 5 | a0001c0001t0016g0110a0001c0013t0001g0047a0001c0013t0048g0046others(2): Show | 5 | HG01884.hp1 HG02572.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.3781+8454A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27788309 | ||||||
chr22:27788325
|
G | A | 1 | a0001c0001t0002g0213 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3781+8438C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27788325 | ||||||
chr22:27788340
|
G | T | 3 | a0001c0001t0001g0093a0001c0001t0008g0056a0003c0004t0001g0241 | 3 | HG00140.hp1 HG01167.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3781+8423C>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27788340 | ||||||
chr22:27788363
|
A | G | 5 | a0001c0001t0016g0110a0001c0013t0001g0047a0001c0013t0048g0046others(2): Show | 5 | HG01884.hp1 HG02572.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.3781+8400T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27788363 | ||||||
chr22:27788364
|
C | T | 2 | a0001c0001t0002g0070a0003c0004t0002g0240 | 2 | HG01192.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.3781+8399G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27788364 | ||||||
chr22:27788454
|
A | G | 1 | a0001c0001t0001g0146 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.3781+8309T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27788454 | ||||||
chr22:27788545
|
C | A | 4 | a0001c0001t0002g0223a0001c0005t0009g0016a0001c0005t0009g0017others(1): Show | 4 | HG01496.hp1 HG01891.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.3781+8218G>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27788545 | ||||||
chr22:27788619
|
CT | C | 12 | a0001c0001t0001g0076a0001c0001t0002g0126a0001c0001t0002g0223others(9): Show | 13 | HG01243.hp1 HG01496.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.3781+8143delA | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27788619 | ||||||
chr22:27788680
|
T | TGTGTGTG others(9): Show |
1 | a0001c0016t0003g0280 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.3781+8067_3781+808 others(20): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27788680 | ||||||
chr22:27788680
|
TGTGTGTG others(9): Show |
T | 5 | a0001c0001t0016g0110a0001c0013t0001g0047a0001c0013t0048g0046others(2): Show | 5 | HG01884.hp1 HG02572.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.3781+8067_3781+808 others(20): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27788680 | ||||||
chr22:27788690
|
T | C | 5 | a0001c0001t0002g0070a0001c0001t0002g0126a0001c0001t0075g0384others(2): Show | 6 | HG01192.hp2 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.3781+8073A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27788690 | ||||||
chr22:27788693
|
A | G | 2 | a0001c0001t0002g0070a0003c0004t0002g0240 | 2 | HG01192.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.3781+8070T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27788693 | ||||||
chr22:27788723
|
G | A | 2 | a0001c0001t0004g0349a0001c0001t0012g0354 | 2 | HG00609.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.3781+8040C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27788723 | ||||||
chr22:27789033
|
G | A | 1 | a0001c0001t0009g0020 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3781+7730C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27789033 | ||||||
chr22:27789251
|
GATCTTCT others(17): Show |
G | 10 | a0001c0001t0003g0303a0001c0001t0003g0342a0001c0001t0004g0346others(7): Show | 10 | HG02015.hp1 HG02523.hp1 NA18964.hp2 others(7): Show |
intron_variant | MODIFIER | c.3781+7488_3781+751 others(28): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27789251 | ||||||
chr22:27789438
|
A | G | 17 | a0001c0001t0001g0107a0001c0001t0001g0119a0001c0001t0002g0062others(14): Show | 17 | HG00438.hp1 HG00558.hp1 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.3781+7325T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27789438 | ||||||
chr22:27789464
|
T | G | 46 | a0001c0001t0001g0128a0001c0001t0001g0209a0001c0001t0001g0210others(43): Show | 46 | HG00438.hp2 HG00733.hp1 HG00741.hp2 others(43): Show |
intron_variant | MODIFIER | c.3781+7299A>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27789464 | ||||||
chr22:27789489
|
C | T | 1 | a0001c0001t0008g0067 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.3781+7274G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27789489 | ||||||
chr22:27789537
|
C | T | 2 | a0001c0014t0018g0374a0001c0014t0018g0375 | 2 | HG02257.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.3781+7226G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27789537 | ||||||
chr22:27789677
|
C | A | 2 | a0001c0014t0018g0374a0001c0014t0018g0375 | 2 | HG02257.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.3781+7086G>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27789677 | ||||||
chr22:27789989
|
G | A | 3 | a0001c0001t0033g0318a0001c0001t0061g0222a0002c0020t0005g0249 | 3 | HG02027.hp2 HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.3781+6774C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27789989 | ||||||
chr22:27790097
|
T | C | 1 | a0004c0007t0001g0270 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.3781+6666A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27790097 | ||||||
chr22:27790112
|
C | T | 1 | a0001c0001t0003g0297 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.3781+6651G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27790112 | ||||||
chr22:27790139
|
G | A | 3 | a0001c0001t0002g0212a0001c0001t0003g0339a0001c0001t0011g0069 | 3 | HG00673.hp2 HG02132.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.3781+6624C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27790139 | ||||||
chr22:27790157
|
C | T | 1 | a0001c0001t0002g0184 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.3781+6606G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27790157 | ||||||
chr22:27790181
|
C | T | 2 | a0003c0004t0001g0247a0003c0004t0002g0246 | 2 | HG02055.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.3781+6582G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27790181 | ||||||
chr22:27790299
|
G | A | 52 | a0001c0001t0001g0064a0001c0001t0001g0180a0001c0001t0001g0183others(49): Show | 53 | HG00280.hp2 HG00323.hp2 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.3781+6464C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27790299 | ||||||
chr22:27790301
|
A | G | 73 | a0001c0001t0001g0064a0001c0001t0001g0107a0001c0001t0001g0119others(70): Show | 74 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.3781+6462T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27790301 | ||||||
chr22:27790369
|
A | G | 1 | a0002c0003t0009g0031 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3781+6394T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27790369 | ||||||
chr22:27790382
|
A | G | 58 | a0001c0001t0001g0064a0001c0001t0001g0180a0001c0001t0001g0183others(55): Show | 59 | HG00280.hp2 HG00323.hp2 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.3781+6381T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27790382 | ||||||
chr22:27790522
|
C | A | 1 | a0001c0001t0004g0335 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.3781+6241G>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27790522 | ||||||
chr22:27790589
|
G | A | 1 | a0011c0017t0003g0361 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.3781+6174C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27790589 | ||||||
chr22:27790787
|
T | C | 53 | a0001c0001t0001g0064a0001c0001t0001g0180a0001c0001t0001g0183others(50): Show | 54 | HG00280.hp2 HG00323.hp2 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.3781+5976A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27790787 | ||||||
chr22:27790847
|
T | A | 1 | a0007c0025t0032g0372 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.3781+5916A>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27790847 | ||||||
chr22:27790958
|
C | G | 1 | a0001c0001t0005g0145 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.3781+5805G>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27790958 | ||||||
chr22:27790971
|
C | T | 26 | a0001c0001t0001g0055a0001c0001t0001g0076a0001c0001t0001g0078others(23): Show | 26 | HG00408.hp2 HG01257.hp1 HG01358.hp1 others(23): Show |
intron_variant | MODIFIER | c.3781+5792G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27790971 | ||||||
chr22:27791318
|
G | A | 1 | a0001c0001t0001g0064 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.3781+5445C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27791318 | ||||||
chr22:27791389
|
G | A | 1 | a0001c0001t0005g0085 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.3781+5374C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27791389 | ||||||
chr22:27791408
|
A | G | 50 | a0001c0001t0001g0064a0001c0001t0001g0180a0001c0001t0001g0183others(47): Show | 50 | HG00280.hp2 HG00323.hp2 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.3781+5355T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27791408 | ||||||
chr22:27791749
|
A | T | 1 | a0001c0001t0002g0116 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3781+5014T>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27791749 | ||||||
chr22:27791785
|
T | C | 2 | a0001c0001t0010g0308a0002c0002t0004g0370 | 2 | HG01515.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.3781+4978A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27791785 | ||||||
chr22:27791790
|
A | T | 1 | a0001c0001t0059g0231 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3781+4973T>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27791790 | ||||||
chr22:27792014
|
C | T | 2 | a0001c0001t0024g0018a0002c0002t0006g0266 | 2 | HG03831.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.3781+4749G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27792014 | ||||||
chr22:27792105
|
A | C | 1 | a0001c0001t0002g0177 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.3781+4658T>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27792105 | ||||||
chr22:27792112
|
A | C | 1 | a0001c0001t0059g0231 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3781+4651T>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27792112 | ||||||
chr22:27792215
|
T | C | 50 | a0001c0001t0001g0064a0001c0001t0001g0180a0001c0001t0001g0183others(47): Show | 50 | HG00280.hp2 HG00323.hp2 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.3781+4548A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27792215 | ||||||
chr22:27792229
|
C | T | 3 | a0001c0001t0002g0086a0001c0001t0004g0295a0001c0001t0065g0294 | 3 | NA18971.hp1 NA19078.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.3781+4534G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27792229 | ||||||
chr22:27792230
|
G | A | 22 | a0001c0001t0001g0074a0001c0001t0002g0068a0001c0001t0002g0177others(19): Show | 22 | HG00621.hp1 HG00673.hp2 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.3781+4533C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27792230 | ||||||
chr22:27792317
|
C | CAT | 26 | a0001c0001t0001g0001a0001c0001t0001g0093a0001c0001t0001g0094others(23): Show | 27 | HG00099.hp2 HG00408.hp1 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.3781+4444_3781+444 others(6): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27792317 | ||||||
chr22:27792317
|
C | CATAT | 15 | a0001c0001t0001g0211a0001c0001t0002g0070a0001c0001t0002g0090others(12): Show | 15 | HG00323.hp1 HG00733.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.3781+4442_3781+444 others(8): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27792317 | ||||||
chr22:27792317
|
C | CATATAT | 13 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0002g0087others(10): Show | 13 | HG01099.hp1 HG01256.hp2 HG01257.hp2 others(10): Show |
intron_variant | MODIFIER | c.3781+4440_3781+444 others(10): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27792317 | ||||||
chr22:27792317
|
C | CATATATA others(3): Show |
7 | a0001c0001t0002g0201a0001c0001t0007g0112a0001c0001t0008g0056others(4): Show | 7 | HG00140.hp1 HG01255.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.3781+4436_3781+444 others(14): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27792317 | ||||||
chr22:27792317
|
CAT | C | 43 | a0001c0001t0001g0064a0001c0001t0001g0187a0001c0001t0001g0188others(40): Show | 43 | HG00280.hp2 HG00323.hp2 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.3781+4444_3781+444 others(6): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27792317 | ||||||
chr22:27792317
|
CATAT | C | 25 | a0001c0001t0001g0055a0001c0001t0001g0076a0001c0001t0001g0111others(22): Show | 25 | HG00639.hp2 HG01884.hp2 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.3781+4442_3781+444 others(8): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27792317 | ||||||
chr22:27792317
|
CATATAT | C | 68 | a0001c0001t0001g0065a0001c0001t0001g0078a0001c0001t0001g0079others(65): Show | 70 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.3781+4440_3781+444 others(10): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27792317 | ||||||
chr22:27792317
|
CATATATA others(1): Show |
C | 84 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0061others(81): Show | 89 | HG00280.hp1 HG00408.hp2 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.3781+4438_3781+444 others(12): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27792317 | ||||||
chr22:27792317
|
CATATATA others(3): Show |
C | 37 | a0001c0001t0001g0074a0001c0001t0001g0107a0001c0001t0001g0119others(34): Show | 37 | HG00438.hp1 HG00558.hp1 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.3781+4436_3781+444 others(14): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27792317 | ||||||
chr22:27792317
|
CATATATA others(5): Show |
C | 8 | a0001c0001t0002g0212a0001c0001t0003g0339a0001c0001t0011g0069others(5): Show | 8 | HG00621.hp1 HG00673.hp2 HG01516.hp2 others(5): Show |
intron_variant | MODIFIER | c.3781+4434_3781+444 others(16): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27792317 | ||||||
chr22:27792317
|
CATATATA others(7): Show |
C | 3 | a0001c0001t0003g0340a0001c0001t0005g0122a0001c0001t0007g0121 | 3 | NA19078.hp1 NA19081.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.3781+4432_3781+444 others(18): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27792317 | ||||||
chr22:27792317
|
CATATATA others(9): Show |
C | 2 | a0001c0001t0007g0173a0001c0001t0050g0174 | 2 | NA18612.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.3781+4430_3781+444 others(20): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27792317 | ||||||
chr22:27792351
|
T | A | 42 | a0001c0001t0001g0064a0001c0001t0001g0180a0001c0001t0001g0183others(39): Show | 42 | HG00280.hp2 HG00323.hp2 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.3781+4412A>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27792351 | ||||||
chr22:27792351
|
T | TAA | 3 | a0001c0001t0002g0075a0001c0001t0003g0320a0001c0001t0062g0063 | 3 | HG00738.hp2 HG01175.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.3781+4411_3781+441 others(6): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27792351 | ||||||
chr22:27792409
|
C | T | 2 | a0001c0001t0003g0301a0001c0001t0003g0341 | 2 | HG02083.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.3781+4354G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27792409 | ||||||
chr22:27792552
|
G | A | 2 | a0001c0001t0002g0070a0003c0004t0002g0240 | 2 | HG01192.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.3781+4211C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27792552 | ||||||
chr22:27792653
|
C | T | 3 | a0001c0001t0009g0020a0001c0001t0045g0042a0001c0001t0069g0373 | 3 | HG02055.hp2 HG02145.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.3781+4110G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27792653 | ||||||
chr22:27792707
|
G | A | 1 | a0001c0001t0002g0108 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.3781+4056C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27792707 | ||||||
chr22:27792709
|
G | A | 1 | a0001c0001t0005g0109 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.3781+4054C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27792709 | ||||||
chr22:27792894
|
C | G | 7 | a0001c0001t0002g0213a0001c0001t0009g0020a0001c0001t0045g0042others(4): Show | 8 | HG02055.hp2 HG02145.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.3781+3869G>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27792894 | ||||||
chr22:27792896
|
C | G | 14 | a0001c0001t0001g0124a0001c0001t0001g0229a0001c0001t0002g0070others(11): Show | 14 | HG01192.hp2 HG01243.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.3781+3867G>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27792896 | ||||||
chr22:27792911
|
C | T | 3 | a0001c0001t0002g0126a0001c0001t0075g0384a0001c0009t0021g0006 | 4 | HG02895.hp1 HG02897.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.3781+3852G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27792911 | ||||||
chr22:27793183
|
C | T | 8 | a0001c0001t0001g0074a0001c0001t0002g0068a0001c0001t0002g0177others(5): Show | 8 | HG01081.hp1 HG02040.hp2 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.3781+3580G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27793183 | ||||||
chr22:27793299
|
CTG | C | 12 | a0001c0001t0001g0124a0001c0001t0001g0229a0001c0001t0002g0125others(9): Show | 12 | HG01243.hp2 HG01891.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.3781+3462_3781+346 others(6): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27793299 | ||||||
chr22:27793331
|
ATTACAAA others(47): Show |
A | 14 | a0001c0001t0001g0124a0001c0001t0001g0229a0001c0001t0002g0070others(11): Show | 14 | HG01192.hp2 HG01243.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.3781+3378_3781+343 others(58): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27793331 | ||||||
chr22:27793399
|
C | A | 6 | a0001c0001t0016g0110a0001c0001t0021g0073a0001c0013t0001g0047others(3): Show | 6 | HG01884.hp1 HG02572.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.3781+3364G>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27793399 | ||||||
chr22:27793468
|
C | T | 4 | a0001c0001t0002g0126a0001c0001t0075g0384a0001c0009t0021g0006others(1): Show | 5 | HG02895.hp1 HG02897.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.3781+3295G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27793468 | ||||||
chr22:27793681
|
T | C | 7 | a0001c0001t0002g0223a0001c0005t0002g0048a0001c0005t0006g0049others(4): Show | 7 | HG01243.hp1 HG01496.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.3781+3082A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27793681 | ||||||
chr22:27793699
|
T | C | 25 | a0001c0001t0001g0124a0001c0001t0001g0229a0001c0001t0002g0070others(22): Show | 25 | HG01192.hp2 HG01243.hp2 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.3781+3064A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27793699 | ||||||
chr22:27793720
|
CA | C | 9 | a0001c0001t0001g0074a0001c0001t0002g0068a0001c0001t0002g0177others(6): Show | 9 | HG01081.hp1 HG01993.hp1 HG02040.hp2 others(6): Show |
intron_variant | MODIFIER | c.3781+3042delT | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27793720 | ||||||
chr22:27793756
|
C | T | 1 | a0001c0001t0009g0020 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3781+3007G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27793756 | ||||||
chr22:27793834
|
G | A | 10 | a0001c0001t0001g0124a0001c0001t0001g0229a0001c0001t0002g0125others(7): Show | 10 | HG02109.hp2 HG02809.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.3781+2929C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27793834 | ||||||
chr22:27793839
|
C | T | 3 | a0001c0001t0002g0086a0001c0001t0004g0295a0001c0001t0065g0294 | 3 | NA18971.hp1 NA19078.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.3781+2924G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27793839 | ||||||
chr22:27793899
|
G | A | 9 | a0001c0001t0001g0074a0001c0001t0001g0204a0001c0001t0002g0068others(6): Show | 9 | HG01081.hp1 HG01361.hp1 HG01993.hp1 others(6): Show |
intron_variant | MODIFIER | c.3781+2864C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27793899 | ||||||
chr22:27793960
|
A | C | 10 | a0001c0001t0001g0124a0001c0001t0001g0229a0001c0001t0002g0125others(7): Show | 10 | HG02109.hp2 HG02809.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.3781+2803T>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27793960 | ||||||
chr22:27793988
|
G | A | 2 | a0001c0001t0002g0070a0003c0004t0002g0240 | 2 | HG01192.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.3781+2775C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27793988 | ||||||
chr22:27794178
|
A | G | 1 | a0001c0001t0001g0235 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3781+2585T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27794178 | ||||||
chr22:27794217
|
G | A | 3 | a0001c0001t0004g0334a0001c0001t0004g0335a0001c0001t0025g0039 | 3 | HG01346.hp1 HG01358.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.3781+2546C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27794217 | ||||||
chr22:27794246
|
A | G | 22 | a0001c0001t0001g0055a0001c0001t0001g0076a0001c0001t0001g0078others(19): Show | 22 | HG00408.hp2 HG01257.hp1 HG01358.hp1 others(19): Show |
intron_variant | MODIFIER | c.3781+2517T>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27794246 | ||||||
chr22:27794426
|
A | T | 46 | a0001c0001t0001g0064a0001c0001t0001g0180a0001c0001t0001g0183others(43): Show | 46 | HG00280.hp2 HG00323.hp2 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.3781+2337T>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27794426 | ||||||
chr22:27794463
|
C | A | 1 | a0001c0001t0001g0111 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.3781+2300G>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27794463 | ||||||
chr22:27794493
|
G | A | 11 | a0001c0001t0002g0212a0001c0001t0003g0300a0001c0001t0003g0338others(8): Show | 11 | HG00621.hp1 HG00673.hp2 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.3781+2270C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27794493 | ||||||
chr22:27794498
|
G | A | 2 | a0001c0001t0008g0067a0001c0012t0020g0276 | 2 | HG00280.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.3781+2265C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27794498 | ||||||
chr22:27794610
|
A | C | 1 | a0001c0001t0002g0232 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3781+2153T>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27794610 | ||||||
chr22:27794743
|
T | C | 1 | a0002c0002t0005g0267 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.3781+2020A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27794743 | ||||||
chr22:27794813
|
TG | T | 196 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0061others(193): Show | 202 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.3781+1949delC | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27794813 | ||||||
chr22:27794814
|
G | GT | 5 | a0001c0005t0002g0050a0001c0005t0016g0053a0001c0005t0028g0051others(2): Show | 5 | HG02451.hp1 HG02970.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.3781+1948dupA | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27794814 | ||||||
chr22:27794814
|
G | T | 4 | a0001c0001t0002g0213a0001c0001t0053g0123a0002c0006t0036g0008others(1): Show | 5 | HG02886.hp1 HG03041.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.3781+1949C>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27794814 | ||||||
chr22:27794816
|
TG | T | 53 | a0001c0001t0001g0064a0001c0001t0001g0180a0001c0001t0001g0183others(50): Show | 53 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.3781+1946delC | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27794816 | ||||||
chr22:27794817
|
G | T | 205 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0061others(202): Show | 212 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(209): Show |
intron_variant | MODIFIER | c.3781+1946C>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27794817 | ||||||
chr22:27794817
|
GT | G | 39 | a0001c0001t0001g0119a0001c0001t0001g0209a0001c0001t0001g0210others(36): Show | 39 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.3781+1945delA | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27794817 | ||||||
chr22:27794821
|
T | G | 252 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0061others(249): Show | 259 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.3781+1942A>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27794821 | ||||||
chr22:27795213
|
C | T | 1 | a0001c0001t0033g0287 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3781+1550G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27795213 | ||||||
chr22:27795289
|
C | T | 2 | a0002c0003t0014g0029a0002c0003t0039g0028 | 2 | HG01884.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.3781+1474G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27795289 | ||||||
chr22:27795517
|
G | A | 2 | a0001c0001t0008g0228a0001c0001t0032g0360 | 2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.3781+1246C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27795517 | ||||||
chr22:27795522
|
G | T | 1 | a0001c0001t0011g0069 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.3781+1241C>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27795522 | ||||||
chr22:27795713
|
C | CTA | 8 | a0001c0001t0001g0235a0001c0005t0043g0037a0001c0010t0040g0012others(5): Show | 8 | HG01884.hp2 HG02055.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.3781+1048_3781+104 others(6): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27795713 | ||||||
chr22:27795722
|
T | TAC | 90 | a0001c0001t0001g0065a0001c0001t0001g0205a0001c0001t0001g0207others(87): Show | 90 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.3781+1039_3781+104 others(6): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27795722 | ||||||
chr22:27795722
|
TAC | T | 9 | a0001c0001t0001g0229a0001c0001t0002g0068a0001c0001t0002g0230others(6): Show | 9 | HG01081.hp1 HG01243.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.3781+1039_3781+104 others(6): Show |
MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27795722 | ||||||
chr22:27795724
|
C | T | 21 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0074others(18): Show | 21 | HG00408.hp1 HG00738.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.3781+1039G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27795724 | ||||||
chr22:27795726
|
C | T | 1 | a0001c0001t0069g0373 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3781+1037G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27795726 | ||||||
chr22:27795740
|
C | T | 1 | a0001c0001t0023g0019 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3781+1023G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27795740 | ||||||
chr22:27795858
|
T | G | 43 | a0001c0001t0001g0229a0001c0001t0001g0235a0001c0001t0002g0230others(40): Show | 43 | HG01099.hp1 HG01243.hp1 HG01243.hp2 others(40): Show |
intron_variant | MODIFIER | c.3781+905A>C | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27795858 | ||||||
chr22:27795907
|
G | T | 14 | a0001c0001t0001g0061a0001c0001t0001g0064a0001c0001t0001g0065others(11): Show | 14 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(11): Show |
intron_variant | MODIFIER | c.3781+856C>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27795907 | ||||||
chr22:27795938
|
C | T | 1 | a0001c0001t0046g0038 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.3781+825G>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27795938 | ||||||
chr22:27796008
|
T | C | 2 | a0001c0001t0009g0020a0001c0001t0023g0019 | 2 | HG02145.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.3781+755A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27796008 | ||||||
chr22:27796435
|
G | A | 21 | a0001c0005t0002g0048a0001c0005t0002g0050a0001c0005t0002g0054others(18): Show | 21 | HG01243.hp1 HG01243.hp2 HG01496.hp2 others(18): Show |
intron_variant | MODIFIER | c.3781+328C>T | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27796435 | ||||||
chr22:27796555
|
T | C | 1 | a0002c0020t0005g0249 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.3781+208A>G | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27796555 | ||||||
chr22:27796563
|
G | T | 1 | a0001c0001t0001g0055 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.3781+200C>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27796563 | ||||||
chr22:27796580
|
G | T | 1 | a0001c0001t0004g0281 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.3781+183C>A | MN1 | ENSG00000169184.7 | transcript | ENST00000302326.5 | protein_coding | 1/1 | chr22 | 27796580 |