geneid | 25813 |
---|---|
ensemblid | ENSG00000100347.15 |
hgncid | 24276 |
symbol | SAMM50 |
name | SAMM50 sorting and assembly machinery component |
refseq_nuc | NM_015380.5 |
refseq_prot | NP_056195.3 |
ensembl_nuc | ENST00000350028.5 |
ensembl_prot | ENSP00000345445.4 |
mane_status | MANE Select |
chr | chr22 |
start | 43955442 |
end | 43996529 |
strand | + |
ver | v1.2 |
region | chr22:43955442-43996529 |
region5000 | chr22:43950442-44001529 |
regionname0 | SAMM50_chr22_43955442_43996529 |
regionname5000 | SAMM50_chr22_43950442_44001529 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 469 | 198 | 75 | 25 | 73 | 5 | 20 | 55 | SAMM50_chr22_43950442_44001529 | SAMM50 | copy fasta | chr22 | 43950442 | 44001529 |
a0002 | 0/1 | 469 | 100 | 10 | 24 | 54 | 6 | 5 | 40 | SAMM50_chr22_43950442_44001529 | SAMM50 | copy fasta | chr22 | 43950442 | 44001529 |
a0003 | 1/0 | 469 | 78 | 9 | 21 | 28 | 5 | 14 | 21 | SAMM50_chr22_43950442_44001529 | SAMM50 | copy fasta | chr22 | 43950442 | 44001529 |
a0004 | 0/0 | 469 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | copy fasta | chr22 | 43950442 | 44001529 |
a0005 | 0/0 | 469 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | copy fasta | chr22 | 43950442 | 44001529 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 1410 | 93 | 7 | 22 | 53 | 5 | 5 | SAMM50_chr22_43950442_44001529 | SAMM50 | copy fasta | chr22 | 43950442 | 44001529 |
c0002 | 0/0 | 1410 | 77 | 36 | 6 | 22 | 1 | 12 | SAMM50_chr22_43950442_44001529 | SAMM50 | copy fasta | chr22 | 43950442 | 44001529 |
c0003 | 1/0 | 1410 | 75 | 9 | 21 | 25 | 5 | 14 | SAMM50_chr22_43950442_44001529 | SAMM50 | copy fasta | chr22 | 43950442 | 44001529 |
c0004 | 0/0 | 1410 | 73 | 3 | 10 | 50 | 3 | 7 | SAMM50_chr22_43950442_44001529 | SAMM50 | copy fasta | chr22 | 43950442 | 44001529 |
c0005 | 0/0 | 1410 | 10 | 10 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | copy fasta | chr22 | 43950442 | 44001529 |
c0006 | 0/0 | 1410 | 10 | 7 | 2 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | copy fasta | chr22 | 43950442 | 44001529 |
c0007 | 0/0 | 1410 | 9 | 3 | 5 | 0 | 1 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | copy fasta | chr22 | 43950442 | 44001529 |
c0008 | 0/0 | 1410 | 9 | 8 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | copy fasta | chr22 | 43950442 | 44001529 |
c0009 | 0/0 | 1410 | 3 | 2 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | copy fasta | chr22 | 43950442 | 44001529 |
c0010 | 0/0 | 1410 | 3 | 3 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | copy fasta | chr22 | 43950442 | 44001529 |
c0011 | 0/0 | 1410 | 3 | 2 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | copy fasta | chr22 | 43950442 | 44001529 |
c0012 | 0/0 | 1410 | 3 | 1 | 1 | 0 | 1 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | copy fasta | chr22 | 43950442 | 44001529 |
c0013 | 0/0 | 1410 | 2 | 2 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | copy fasta | chr22 | 43950442 | 44001529 |
c0014 | 0/0 | 1410 | 2 | 0 | 0 | 2 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | copy fasta | chr22 | 43950442 | 44001529 |
c0015 | 0/0 | 1410 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | copy fasta | chr22 | 43950442 | 44001529 |
c0016 | 0/0 | 1410 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | copy fasta | chr22 | 43950442 | 44001529 |
c0017 | 0/0 | 1410 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | copy fasta | chr22 | 43950442 | 44001529 |
c0018 | 0/0 | 1410 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | copy fasta | chr22 | 43950442 | 44001529 |
c0019 | 0/0 | 1410 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | copy fasta | chr22 | 43950442 | 44001529 |
c0020 | 0/0 | 1410 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | copy fasta | chr22 | 43950442 | 44001529 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 283 | 319 | 70 | 65 | 139 | 15 | 28 | SAMM50_chr22_43950442_44001529 | SAMM50 | copy fasta | chr22 | 43950442 | 44001529 |
t0002 | 0/0 | 283 | 54 | 21 | 5 | 16 | 1 | 11 | SAMM50_chr22_43950442_44001529 | SAMM50 | copy fasta | chr22 | 43950442 | 44001529 |
t0003 | 0/0 | 283 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | copy fasta | chr22 | 43950442 | 44001529 |
t0004 | 0/0 | 283 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | copy fasta | chr22 | 43950442 | 44001529 |
t0005 | 0/0 | 283 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | copy fasta | chr22 | 43950442 | 44001529 |
t0006 | 0/0 | 283 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | copy fasta | chr22 | 43950442 | 44001529 |
t0007 | 0/0 | 283 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | copy fasta | chr22 | 43950442 | 44001529 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0003 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0004 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0006 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0008 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0010 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0011 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0012 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0014 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0015 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0025 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0027 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0086 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0222 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002 | 0/0 | 1410 | 77 | 36 | 6 | 22 | 1 | 12 | SAMM50_chr22_43950442_44001529 | SAMM50 | copy fasta | chr22 | 43950442 | 44001529 |
a0001c0004 | 0/0 | 1410 | 73 | 3 | 10 | 50 | 3 | 7 | SAMM50_chr22_43950442_44001529 | SAMM50 | copy fasta | chr22 | 43950442 | 44001529 |
a0001c0005 | 0/0 | 1410 | 10 | 10 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | copy fasta | chr22 | 43950442 | 44001529 |
a0001c0006 | 0/0 | 1410 | 10 | 7 | 2 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | copy fasta | chr22 | 43950442 | 44001529 |
a0001c0007 | 0/0 | 1410 | 9 | 3 | 5 | 0 | 1 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | copy fasta | chr22 | 43950442 | 44001529 |
a0001c0008 | 0/0 | 1410 | 9 | 8 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | copy fasta | chr22 | 43950442 | 44001529 |
a0001c0009 | 0/0 | 1410 | 3 | 2 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | copy fasta | chr22 | 43950442 | 44001529 |
a0001c0010 | 0/0 | 1410 | 3 | 3 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | copy fasta | chr22 | 43950442 | 44001529 |
a0001c0013 | 0/0 | 1410 | 2 | 2 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | copy fasta | chr22 | 43950442 | 44001529 |
a0001c0017 | 0/0 | 1410 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | copy fasta | chr22 | 43950442 | 44001529 |
a0001c0020 | 0/0 | 1410 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | copy fasta | chr22 | 43950442 | 44001529 |
a0002c0001 | 0/1 | 1410 | 93 | 7 | 22 | 53 | 5 | 5 | SAMM50_chr22_43950442_44001529 | SAMM50 | copy fasta | chr22 | 43950442 | 44001529 |
a0002c0011 | 0/0 | 1410 | 3 | 2 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | copy fasta | chr22 | 43950442 | 44001529 |
a0002c0012 | 0/0 | 1410 | 3 | 1 | 1 | 0 | 1 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | copy fasta | chr22 | 43950442 | 44001529 |
a0002c0018 | 0/0 | 1410 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | copy fasta | chr22 | 43950442 | 44001529 |
a0003c0003 | 1/0 | 1410 | 75 | 9 | 21 | 25 | 5 | 14 | SAMM50_chr22_43950442_44001529 | SAMM50 | copy fasta | chr22 | 43950442 | 44001529 |
a0003c0014 | 0/0 | 1410 | 2 | 0 | 0 | 2 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | copy fasta | chr22 | 43950442 | 44001529 |
a0003c0016 | 0/0 | 1410 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | copy fasta | chr22 | 43950442 | 44001529 |
a0004c0015 | 0/0 | 1410 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | copy fasta | chr22 | 43950442 | 44001529 |
a0005c0019 | 0/0 | 1410 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | copy fasta | chr22 | 43950442 | 44001529 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0001 | 0/0 | 1692 | 23 | 14 | 1 | 7 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | copy fasta | chr22 | 43950442 | 44001529 |
a0001c0002t0002 | 0/0 | 1692 | 53 | 21 | 5 | 15 | 1 | 11 | SAMM50_chr22_43950442_44001529 | SAMM50 | copy fasta | chr22 | 43950442 | 44001529 |
a0001c0002t0004 | 0/0 | 1692 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | copy fasta | chr22 | 43950442 | 44001529 |
a0001c0004t0001 | 0/0 | 1692 | 72 | 3 | 10 | 49 | 3 | 7 | SAMM50_chr22_43950442_44001529 | SAMM50 | copy fasta | chr22 | 43950442 | 44001529 |
a0001c0004t0002 | 0/0 | 1692 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | copy fasta | chr22 | 43950442 | 44001529 |
a0001c0005t0001 | 0/0 | 1692 | 10 | 10 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | copy fasta | chr22 | 43950442 | 44001529 |
a0001c0006t0001 | 0/0 | 1692 | 10 | 7 | 2 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | copy fasta | chr22 | 43950442 | 44001529 |
a0001c0007t0001 | 0/0 | 1692 | 7 | 1 | 5 | 0 | 1 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | copy fasta | chr22 | 43950442 | 44001529 |
a0001c0007t0003 | 0/0 | 1692 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | copy fasta | chr22 | 43950442 | 44001529 |
a0001c0007t0005 | 0/0 | 1692 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | copy fasta | chr22 | 43950442 | 44001529 |
a0001c0008t0001 | 0/0 | 1692 | 9 | 8 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | copy fasta | chr22 | 43950442 | 44001529 |
a0001c0009t0001 | 0/0 | 1692 | 3 | 2 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | copy fasta | chr22 | 43950442 | 44001529 |
a0001c0010t0001 | 0/0 | 1692 | 3 | 3 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | copy fasta | chr22 | 43950442 | 44001529 |
a0001c0013t0001 | 0/0 | 1692 | 2 | 2 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | copy fasta | chr22 | 43950442 | 44001529 |
a0001c0017t0006 | 0/0 | 1692 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | copy fasta | chr22 | 43950442 | 44001529 |
a0001c0020t0001 | 0/0 | 1692 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | copy fasta | chr22 | 43950442 | 44001529 |
a0002c0001t0001 | 0/1 | 1692 | 93 | 7 | 22 | 53 | 5 | 5 | SAMM50_chr22_43950442_44001529 | SAMM50 | copy fasta | chr22 | 43950442 | 44001529 |
a0002c0011t0001 | 0/0 | 1692 | 3 | 2 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | copy fasta | chr22 | 43950442 | 44001529 |
a0002c0012t0001 | 0/0 | 1692 | 3 | 1 | 1 | 0 | 1 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | copy fasta | chr22 | 43950442 | 44001529 |
a0002c0018t0001 | 0/0 | 1692 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | copy fasta | chr22 | 43950442 | 44001529 |
a0003c0003t0001 | 1/0 | 1692 | 75 | 9 | 21 | 25 | 5 | 14 | SAMM50_chr22_43950442_44001529 | SAMM50 | copy fasta | chr22 | 43950442 | 44001529 |
a0003c0014t0001 | 0/0 | 1692 | 2 | 0 | 0 | 2 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | copy fasta | chr22 | 43950442 | 44001529 |
a0003c0016t0001 | 0/0 | 1692 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | copy fasta | chr22 | 43950442 | 44001529 |
a0004c0015t0001 | 0/0 | 1692 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | copy fasta | chr22 | 43950442 | 44001529 |
a0005c0019t0007 | 0/0 | 1692 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | copy fasta | chr22 | 43950442 | 44001529 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0002t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0002t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0002t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0002t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0002t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0002t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0002t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0002t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0002t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0002t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0002t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0002t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0002t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0002t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0002t0002g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0002t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0002t0002g0025 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0002t0002g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0002t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0002t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0002t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0002t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0002t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0002t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0002t0002g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0002t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0002t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0002t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0002t0002g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0002t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0002t0002g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0002t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0002t0002g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0002t0002g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0002t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0002t0002g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0002t0002g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0002t0002g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0002t0002g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0002t0002g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0002t0002g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0002t0002g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0002t0002g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0002t0002g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0002t0002g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0002t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0002t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0002t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0002t0002g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0002t0002g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0002t0002g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0002t0002g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0002t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0002t0002g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0002t0002g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0002t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0002t0002g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0002t0002g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0002t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0002t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0002t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0002t0002g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0002t0004g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0004t0001g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0004t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0004t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0004t0001g0014 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0004t0001g0015 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0004t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0004t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0004t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0004t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0004t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0004t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0004t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0004t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0004t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0004t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0004t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0004t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0004t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0004t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0004t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0004t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0004t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0004t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0004t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0004t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0004t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0004t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0004t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0004t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0004t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0004t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0004t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0004t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0004t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0004t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0004t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0004t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0004t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0004t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0004t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0004t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0004t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0004t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0004t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0004t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0004t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0004t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0004t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0004t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0004t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0004t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0004t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0004t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0004t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0004t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0004t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0004t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0004t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0004t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0004t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0004t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0004t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0004t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0004t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0004t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0005t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0005t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0005t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0005t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0005t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0005t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0005t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0005t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0005t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0006t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0006t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0006t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0006t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0006t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0006t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0006t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0006t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0006t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0006t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0007t0001g0027 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0007t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0007t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0007t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0007t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0007t0003g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0007t0005g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0008t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0008t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0008t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0008t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0008t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0008t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0008t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0008t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0008t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0009t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0009t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0009t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0010t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0010t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0010t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0013t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0013t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0017t0006g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0001c0020t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0006 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0222 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0011t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0011t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0011t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0012t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0012t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0012t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0002c0018t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0003c0003t0001g0001 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0003c0003t0001g0003 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0003c0003t0001g0004 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0003c0003t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0003c0003t0001g0008 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0003c0003t0001g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0003c0003t0001g0010 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0003c0003t0001g0011 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0003c0003t0001g0012 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0003c0003t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0003c0003t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0003c0003t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0003c0003t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0003c0003t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0003c0003t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0003c0003t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0003c0003t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0003c0003t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0003c0003t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0003c0003t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0003c0003t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0003c0003t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0003c0003t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0003c0003t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0003c0003t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0003c0003t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0003c0003t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0003c0003t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0003c0003t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0003c0003t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0003c0003t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0003c0003t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0003c0003t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0003c0003t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0003c0003t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0003c0003t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0003c0003t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0003c0003t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0003c0003t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0003c0003t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0003c0003t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0003c0003t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0003c0003t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0003c0003t0001g0086 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0003c0003t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0003c0003t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0003c0003t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0003c0003t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0003c0003t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0003c0003t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0003c0003t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0003c0003t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0003c0003t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0003c0003t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0003c0003t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0003c0003t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0003c0003t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0003c0003t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0003c0003t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0003c0003t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0003c0014t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0003c0014t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0003c0016t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0004c0015t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
a0005c0019t0007g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0004 | t0001 | g0159 | EUR | GBR | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG00099 | hp2 | a0001 | c0002 | t0002 | g0305 | EUR | GBR | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG00140 | hp1 | a0003 | c0003 | t0001 | g0003 | EUR | GBR | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG00140 | hp2 | a0002 | c0001 | t0001 | g0186 | EUR | GBR | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG00280 | hp1 | a0002 | c0012 | t0001 | g0153 | EUR | FIN | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG00280 | hp2 | a0001 | c0007 | t0001 | g0027 | EUR | FIN | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG00323 | hp1 | a0001 | c0004 | t0001 | g0114 | EUR | FIN | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG00323 | hp2 | a0002 | c0001 | t0001 | g0217 | EUR | FIN | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG00408 | hp1 | a0003 | c0014 | t0001 | g0071 | EAS | CHS | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG00408 | hp2 | a0002 | c0001 | t0001 | g0226 | EAS | CHS | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG00423 | hp1 | a0001 | c0002 | t0001 | g0281 | EAS | CHS | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG00423 | hp2 | a0001 | c0004 | t0001 | g0170 | EAS | CHS | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG00438 | hp1 | a0004 | c0015 | t0001 | g0078 | EAS | CHS | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG00438 | hp2 | a0002 | c0001 | t0001 | g0213 | EAS | CHS | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG00544 | hp1 | a0001 | c0002 | t0002 | g0311 | EAS | CHS | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG00544 | hp2 | a0001 | c0004 | t0001 | g0172 | EAS | CHS | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG00558 | hp1 | a0001 | c0002 | t0002 | g0315 | EAS | CHS | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG00558 | hp2 | a0003 | c0003 | t0001 | g0046 | EAS | CHS | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG00609 | hp1 | a0001 | c0004 | t0001 | g0005 | EAS | CHS | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG00609 | hp2 | a0002 | c0001 | t0001 | g0253 | EAS | CHS | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG00621 | hp1 | a0003 | c0003 | t0001 | g0080 | EAS | CHS | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG00621 | hp2 | a0002 | c0001 | t0001 | g0210 | EAS | CHS | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG00639 | hp1 | a0002 | c0011 | t0001 | g0248 | AMR | PUR | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG00639 | hp2 | a0002 | c0001 | t0001 | g0227 | AMR | PUR | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG00642 | hp1 | a0003 | c0003 | t0001 | g0084 | AMR | PUR | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG00642 | hp2 | a0003 | c0003 | t0001 | g0087 | AMR | PUR | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG00733 | hp1 | a0003 | c0003 | t0001 | g0325 | AMR | PUR | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG00733 | hp2 | a0001 | c0007 | t0001 | g0027 | AMR | PUR | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG00735 | hp1 | a0001 | c0004 | t0001 | g0142 | AMR | PUR | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG00735 | hp2 | a0001 | c0002 | t0002 | g0292 | AMR | PUR | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG00738 | hp1 | a0002 | c0001 | t0001 | g0017 | AMR | PUR | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG00738 | hp2 | a0001 | c0004 | t0001 | g0131 | AMR | PUR | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG00741 | hp1 | a0002 | c0001 | t0001 | g0214 | AMR | PUR | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG00741 | hp2 | a0001 | c0004 | t0001 | g0173 | AMR | PUR | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG01070 | hp1 | a0001 | c0002 | t0002 | g0300 | AMR | PUR | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG01070 | hp2 | a0001 | c0007 | t0001 | g0322 | AMR | PUR | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG01071 | hp1 | a0001 | c0007 | t0001 | g0323 | AMR | PUR | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG01071 | hp2 | a0003 | c0003 | t0001 | g0001 | AMR | PUR | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG01074 | hp1 | a0002 | c0001 | t0001 | g0017 | AMR | PUR | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG01074 | hp2 | a0002 | c0001 | t0001 | g0219 | AMR | PUR | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG01081 | hp1 | a0003 | c0003 | t0001 | g0089 | AMR | PUR | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG01081 | hp2 | a0001 | c0004 | t0001 | g0129 | AMR | PUR | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG01099 | hp1 | a0003 | c0003 | t0001 | g0004 | AMR | PUR | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG01099 | hp2 | a0002 | c0001 | t0001 | g0196 | AMR | PUR | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG01109 | hp1 | a0001 | c0007 | t0001 | g0028 | AMR | PUR | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG01109 | hp2 | a0001 | c0008 | t0001 | g0177 | AMR | PUR | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG01167 | hp1 | a0001 | c0006 | t0001 | g0107 | AMR | PUR | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG01167 | hp2 | a0003 | c0003 | t0001 | g0069 | AMR | PUR | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG01169 | hp1 | a0003 | c0003 | t0001 | g0059 | AMR | PUR | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG01169 | hp2 | a0001 | c0006 | t0001 | g0104 | AMR | PUR | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG01175 | hp1 | a0001 | c0004 | t0001 | g0171 | AMR | PUR | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG01175 | hp2 | a0003 | c0003 | t0001 | g0088 | AMR | PUR | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG01192 | hp1 | a0001 | c0002 | t0002 | g0296 | AMR | PUR | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG01192 | hp2 | a0002 | c0001 | t0001 | g0220 | AMR | PUR | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG01243 | hp1 | a0001 | c0002 | t0002 | g0336 | AMR | PUR | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG01243 | hp2 | a0002 | c0001 | t0001 | g0039 | AMR | PUR | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG01255 | hp1 | a0002 | c0001 | t0001 | g0240 | AMR | CLM | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG01255 | hp2 | a0001 | c0007 | t0001 | g0028 | AMR | CLM | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG01257 | hp1 | a0003 | c0003 | t0001 | g0003 | AMR | CLM | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG01257 | hp2 | a0002 | c0001 | t0001 | g0234 | AMR | CLM | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG01258 | hp1 | a0003 | c0003 | t0001 | g0003 | AMR | CLM | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG01258 | hp2 | a0002 | c0001 | t0001 | g0006 | AMR | CLM | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG01261 | hp1 | a0002 | c0001 | t0001 | g0204 | AMR | CLM | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG01261 | hp2 | a0001 | c0002 | t0002 | g0282 | AMR | CLM | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG01346 | hp1 | a0003 | c0003 | t0001 | g0011 | AMR | CLM | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG01346 | hp2 | a0001 | c0004 | t0001 | g0135 | AMR | CLM | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG01358 | hp1 | a0001 | c0004 | t0001 | g0121 | AMR | CLM | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG01358 | hp2 | a0003 | c0003 | t0001 | g0001 | AMR | CLM | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG01361 | hp1 | a0002 | c0001 | t0001 | g0233 | AMR | CLM | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG01361 | hp2 | a0002 | c0001 | t0001 | g0238 | AMR | CLM | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG01433 | hp1 | a0001 | c0009 | t0001 | g0053 | AMR | CLM | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG01433 | hp2 | a0002 | c0012 | t0001 | g0149 | AMR | CLM | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG01496 | hp1 | a0001 | c0004 | t0001 | g0117 | AMR | CLM | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG01496 | hp2 | a0003 | c0003 | t0001 | g0066 | AMR | CLM | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG01515 | hp1 | a0002 | c0001 | t0001 | g0209 | EUR | IBS | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG01515 | hp2 | a0003 | c0003 | t0001 | g0008 | EUR | IBS | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG01517 | hp1 | a0003 | c0003 | t0001 | g0008 | EUR | IBS | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG01517 | hp2 | a0001 | c0004 | t0001 | g0123 | EUR | IBS | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG01891 | hp1 | a0001 | c0002 | t0001 | g0016 | AFR | ACB | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG01891 | hp2 | a0002 | c0001 | t0001 | g0192 | AFR | ACB | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG01934 | hp1 | a0002 | c0001 | t0001 | g0246 | AMR | PEL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG01934 | hp2 | a0001 | c0002 | t0001 | g0167 | AMR | PEL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG01943 | hp1 | a0001 | c0004 | t0001 | g0147 | AMR | PEL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG01943 | hp2 | a0003 | c0003 | t0001 | g0324 | AMR | PEL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG01952 | hp1 | a0002 | c0001 | t0001 | g0006 | AMR | PEL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG01952 | hp2 | a0002 | c0001 | t0001 | g0245 | AMR | PEL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG01978 | hp1 | a0002 | c0001 | t0001 | g0006 | AMR | PEL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG01978 | hp2 | a0003 | c0003 | t0001 | g0057 | AMR | PEL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG01981 | hp1 | a0002 | c0001 | t0001 | g0244 | AMR | PEL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG01981 | hp2 | a0003 | c0003 | t0001 | g0001 | AMR | PEL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG01993 | hp1 | a0003 | c0003 | t0001 | g0054 | AMR | PEL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG01993 | hp2 | a0002 | c0001 | t0001 | g0021 | AMR | PEL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02015 | hp1 | a0002 | c0001 | t0001 | g0254 | EAS | KHV | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02015 | hp2 | a0003 | c0003 | t0001 | g0090 | EAS | KHV | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02027 | hp1 | a0002 | c0001 | t0001 | g0231 | EAS | KHV | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02027 | hp2 | a0003 | c0003 | t0001 | g0082 | EAS | KHV | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02040 | hp1 | a0002 | c0001 | t0001 | g0228 | EAS | KHV | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02040 | hp2 | a0001 | c0002 | t0002 | g0314 | EAS | KHV | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02055 | hp1 | a0001 | c0006 | t0001 | g0109 | AFR | ACB | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02055 | hp2 | a0001 | c0005 | t0001 | g0334 | AFR | ACB | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02056 | hp1 | a0002 | c0001 | t0001 | g0202 | EAS | KHV | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02056 | hp2 | a0002 | c0001 | t0001 | g0203 | EAS | KHV | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02071 | hp1 | a0001 | c0002 | t0002 | g0184 | EAS | KHV | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02071 | hp2 | a0001 | c0004 | t0001 | g0041 | EAS | KHV | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02074 | hp1 | a0001 | c0004 | t0001 | g0045 | EAS | KHV | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02074 | hp2 | a0001 | c0004 | t0001 | g0151 | EAS | KHV | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02080 | hp1 | a0002 | c0001 | t0001 | g0262 | EAS | KHV | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02080 | hp2 | a0001 | c0004 | t0001 | g0139 | EAS | KHV | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02083 | hp1 | a0002 | c0018 | t0001 | g0224 | EAS | KHV | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02083 | hp2 | a0003 | c0003 | t0001 | g0085 | EAS | KHV | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02129 | hp1 | a0002 | c0001 | t0001 | g0242 | EAS | KHV | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02129 | hp2 | a0003 | c0003 | t0001 | g0010 | EAS | KHV | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02132 | hp1 | a0002 | c0001 | t0001 | g0252 | EAS | KHV | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02132 | hp2 | a0001 | c0002 | t0002 | g0025 | EAS | KHV | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02135 | hp1 | a0001 | c0004 | t0001 | g0002 | EAS | KHV | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02135 | hp2 | a0001 | c0002 | t0002 | g0301 | EAS | KHV | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02145 | hp1 | a0003 | c0003 | t0001 | g0062 | AFR | ACB | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02145 | hp2 | a0003 | c0003 | t0001 | g0056 | AFR | ACB | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02155 | hp1 | a0001 | c0002 | t0002 | g0278 | EAS | CDX | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02155 | hp2 | a0001 | c0004 | t0001 | g0005 | EAS | CDX | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02257 | hp1 | a0001 | c0008 | t0001 | g0179 | AFR | ACB | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02257 | hp2 | a0001 | c0004 | t0001 | g0146 | AFR | ACB | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02258 | hp1 | a0001 | c0002 | t0002 | g0280 | AFR | ACB | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02258 | hp2 | a0001 | c0002 | t0002 | g0040 | AFR | ACB | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02280 | hp1 | a0001 | c0009 | t0001 | g0335 | AFR | ACB | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02280 | hp2 | a0001 | c0002 | t0001 | g0163 | AFR | ACB | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02293 | hp1 | a0003 | c0003 | t0001 | g0092 | AMR | PEL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02293 | hp2 | a0001 | c0004 | t0001 | g0015 | AMR | PEL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02300 | hp1 | a0003 | c0003 | t0001 | g0061 | AMR | PEL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02300 | hp2 | a0002 | c0001 | t0001 | g0207 | AMR | PEL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02451 | hp1 | a0001 | c0006 | t0001 | g0043 | AFR | ACB | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02451 | hp2 | a0003 | c0003 | t0001 | g0048 | AFR | ACB | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02572 | hp1 | a0001 | c0002 | t0002 | g0310 | AFR | GWD | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02572 | hp2 | a0002 | c0001 | t0001 | g0191 | AFR | GWD | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02602 | hp1 | a0001 | c0004 | t0001 | g0317 | SAS | PJL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02602 | hp2 | a0003 | c0003 | t0001 | g0070 | SAS | PJL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02615 | hp1 | a0001 | c0010 | t0001 | g0145 | AFR | GWD | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02615 | hp2 | a0001 | c0005 | t0001 | g0328 | AFR | GWD | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02622 | hp1 | a0001 | c0002 | t0001 | g0164 | AFR | GWD | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02622 | hp2 | a0001 | c0002 | t0002 | g0299 | AFR | GWD | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02630 | hp1 | a0001 | c0002 | t0001 | g0168 | AFR | GWD | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02630 | hp2 | a0002 | c0001 | t0001 | g0194 | AFR | GWD | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02647 | hp1 | a0001 | c0002 | t0001 | g0337 | AFR | GWD | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02647 | hp2 | a0003 | c0003 | t0001 | g0063 | AFR | GWD | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02683 | hp1 | a0003 | c0003 | t0001 | g0003 | SAS | PJL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02683 | hp2 | a0003 | c0003 | t0001 | g0058 | SAS | PJL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02698 | hp1 | a0001 | c0002 | t0002 | g0297 | SAS | PJL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02698 | hp2 | a0001 | c0002 | t0002 | g0295 | SAS | PJL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02717 | hp1 | a0001 | c0008 | t0001 | g0033 | AFR | GWD | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02717 | hp2 | a0001 | c0002 | t0002 | g0023 | AFR | GWD | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02723 | hp1 | a0001 | c0002 | t0002 | g0290 | AFR | GWD | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02723 | hp2 | a0001 | c0013 | t0001 | g0321 | AFR | GWD | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02738 | hp1 | a0003 | c0003 | t0001 | g0077 | SAS | PJL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02738 | hp2 | a0001 | c0004 | t0001 | g0125 | SAS | PJL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02809 | hp1 | a0001 | c0002 | t0001 | g0162 | AFR | GWD | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02809 | hp2 | a0001 | c0007 | t0003 | g0320 | AFR | GWD | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02818 | hp1 | a0001 | c0006 | t0001 | g0103 | AFR | GWD | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02818 | hp2 | a0001 | c0002 | t0002 | g0023 | AFR | GWD | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02886 | hp1 | a0001 | c0005 | t0001 | g0029 | AFR | GWD | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02886 | hp2 | a0001 | c0004 | t0001 | g0014 | AFR | GWD | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02895 | hp1 | a0001 | c0010 | t0001 | g0136 | AFR | GWD | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02895 | hp2 | a0001 | c0002 | t0001 | g0166 | AFR | GWD | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02896 | hp1 | a0001 | c0002 | t0001 | g0161 | AFR | GWD | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02896 | hp2 | a0001 | c0002 | t0002 | g0313 | AFR | GWD | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02897 | hp1 | a0001 | c0002 | t0001 | g0165 | AFR | GWD | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02897 | hp2 | a0001 | c0002 | t0002 | g0312 | AFR | GWD | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02922 | hp1 | a0002 | c0011 | t0001 | g0230 | AFR | ESN | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02922 | hp2 | a0001 | c0002 | t0002 | g0272 | AFR | ESN | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02965 | hp1 | a0001 | c0005 | t0001 | g0329 | AFR | ESN | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02965 | hp2 | a0001 | c0002 | t0001 | g0339 | AFR | ESN | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02970 | hp1 | a0001 | c0005 | t0001 | g0155 | AFR | ESN | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02970 | hp2 | a0001 | c0002 | t0002 | g0283 | AFR | ESN | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02976 | hp1 | a0001 | c0002 | t0002 | g0309 | AFR | ESN | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02976 | hp2 | a0001 | c0004 | t0001 | g0141 | AFR | ESN | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG03017 | hp1 | a0003 | c0003 | t0001 | g0004 | SAS | PJL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG03017 | hp2 | a0002 | c0001 | t0001 | g0258 | SAS | PJL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG03041 | hp1 | a0001 | c0008 | t0001 | g0175 | AFR | GWD | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG03041 | hp2 | a0001 | c0005 | t0001 | g0332 | AFR | GWD | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG03098 | hp1 | a0001 | c0006 | t0001 | g0044 | AFR | MSL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG03098 | hp2 | a0001 | c0020 | t0001 | g0327 | AFR | MSL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG03130 | hp1 | a0001 | c0005 | t0001 | g0333 | AFR | ESN | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG03130 | hp2 | a0001 | c0002 | t0001 | g0338 | AFR | ESN | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG03139 | hp1 | a0001 | c0002 | t0002 | g0288 | AFR | ESN | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG03139 | hp2 | a0001 | c0005 | t0001 | g0330 | AFR | ESN | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG03195 | hp1 | a0001 | c0007 | t0005 | g0034 | AFR | ESN | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG03195 | hp2 | a0001 | c0002 | t0001 | g0189 | AFR | ESN | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG03209 | hp1 | a0002 | c0001 | t0001 | g0205 | AFR | MSL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG03209 | hp2 | a0002 | c0001 | t0001 | g0197 | AFR | MSL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG03225 | hp1 | a0001 | c0002 | t0002 | g0285 | AFR | MSL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG03225 | hp2 | a0001 | c0002 | t0002 | g0286 | AFR | MSL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG03453 | hp1 | a0001 | c0002 | t0004 | g0293 | AFR | MSL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG03453 | hp2 | a0001 | c0013 | t0001 | g0319 | AFR | MSL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG03486 | hp1 | a0001 | c0002 | t0002 | g0271 | AFR | MSL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG03486 | hp2 | a0001 | c0008 | t0001 | g0181 | AFR | MSL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG03490 | hp1 | a0003 | c0003 | t0001 | g0009 | SAS | PJL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG03490 | hp2 | a0001 | c0002 | t0002 | g0274 | SAS | PJL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG03491 | hp1 | a0001 | c0002 | t0002 | g0026 | SAS | PJL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG03491 | hp2 | a0001 | c0006 | t0001 | g0264 | SAS | PJL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG03492 | hp1 | a0003 | c0003 | t0001 | g0009 | SAS | PJL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG03492 | hp2 | a0001 | c0002 | t0002 | g0026 | SAS | PJL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG03516 | hp1 | a0001 | c0007 | t0001 | g0326 | AFR | ESN | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG03516 | hp2 | a0001 | c0002 | t0002 | g0298 | AFR | ESN | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG03540 | hp1 | a0001 | c0006 | t0001 | g0110 | AFR | GWD | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG03540 | hp2 | a0001 | c0005 | t0001 | g0029 | AFR | GWD | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG03579 | hp1 | a0001 | c0002 | t0002 | g0183 | AFR | MSL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG03579 | hp2 | a0001 | c0002 | t0001 | g0016 | AFR | MSL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG03654 | hp1 | a0003 | c0003 | t0001 | g0004 | SAS | PJL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG03654 | hp2 | a0005 | c0019 | t0007 | g0236 | SAS | PJL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG03669 | hp1 | a0001 | c0004 | t0001 | g0134 | SAS | PJL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG03669 | hp2 | a0001 | c0004 | t0001 | g0318 | SAS | PJL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG03688 | hp1 | a0002 | c0001 | t0001 | g0263 | SAS | STU | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG03688 | hp2 | a0003 | c0003 | t0001 | g0010 | SAS | STU | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG03704 | hp1 | a0002 | c0001 | t0001 | g0261 | SAS | PJL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG03704 | hp2 | a0001 | c0002 | t0002 | g0306 | SAS | PJL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG03710 | hp1 | a0002 | c0001 | t0001 | g0243 | SAS | PJL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG03710 | hp2 | a0003 | c0003 | t0001 | g0067 | SAS | PJL | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG03831 | hp1 | a0003 | c0003 | t0001 | g0076 | SAS | BEB | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG03831 | hp2 | a0003 | c0003 | t0001 | g0094 | SAS | BEB | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG03927 | hp1 | a0001 | c0002 | t0002 | g0307 | SAS | BEB | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG03927 | hp2 | a0001 | c0004 | t0001 | g0130 | SAS | BEB | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG03942 | hp1 | a0001 | c0002 | t0002 | g0025 | SAS | BEB | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG03942 | hp2 | a0001 | c0004 | t0001 | g0154 | SAS | BEB | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG04184 | hp1 | a0003 | c0003 | t0001 | g0096 | SAS | BEB | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG04184 | hp2 | a0002 | c0001 | t0001 | g0259 | SAS | BEB | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG04199 | hp1 | a0001 | c0004 | t0001 | g0115 | SAS | STU | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG04199 | hp2 | a0001 | c0002 | t0002 | g0287 | SAS | STU | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG04204 | hp1 | a0001 | c0002 | t0001 | g0269 | SAS | STU | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG04204 | hp2 | a0003 | c0003 | t0001 | g0097 | SAS | STU | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA18522 | hp1 | a0001 | c0005 | t0001 | g0331 | AFR | YRI | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA18522 | hp2 | a0001 | c0010 | t0001 | g0124 | AFR | YRI | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA18747 | hp1 | a0001 | c0004 | t0001 | g0137 | EAS | CHB | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA18747 | hp2 | a0002 | c0001 | t0001 | g0195 | EAS | CHB | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA18906 | hp1 | a0002 | c0001 | t0001 | g0193 | AFR | YRI | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA18906 | hp2 | a0002 | c0001 | t0001 | g0038 | AFR | YRI | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA18939 | hp1 | a0001 | c0002 | t0002 | g0308 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA18939 | hp2 | a0002 | c0001 | t0001 | g0239 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA18940 | hp1 | a0001 | c0004 | t0001 | g0174 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA18940 | hp2 | a0002 | c0001 | t0001 | g0279 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA18943 | hp1 | a0001 | c0004 | t0001 | g0126 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA18943 | hp2 | a0002 | c0001 | t0001 | g0198 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA18945 | hp1 | a0002 | c0001 | t0001 | g0020 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA18945 | hp2 | a0001 | c0004 | t0001 | g0169 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA18946 | hp1 | a0002 | c0001 | t0001 | g0241 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA18946 | hp2 | a0001 | c0004 | t0001 | g0002 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA18947 | hp1 | a0002 | c0001 | t0001 | g0232 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA18947 | hp2 | a0002 | c0001 | t0001 | g0215 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA18949 | hp1 | a0001 | c0004 | t0001 | g0113 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA18949 | hp2 | a0003 | c0003 | t0001 | g0073 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA18951 | hp1 | a0002 | c0001 | t0001 | g0199 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA18951 | hp2 | a0001 | c0004 | t0001 | g0157 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA18952 | hp1 | a0001 | c0004 | t0001 | g0013 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA18952 | hp2 | a0001 | c0004 | t0001 | g0128 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA18953 | hp1 | a0002 | c0001 | t0001 | g0216 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA18953 | hp2 | a0001 | c0004 | t0001 | g0132 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA18959 | hp1 | a0002 | c0001 | t0001 | g0221 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA18959 | hp2 | a0001 | c0004 | t0001 | g0160 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA18963 | hp1 | a0001 | c0004 | t0001 | g0013 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA18963 | hp2 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA18965 | hp1 | a0002 | c0001 | t0001 | g0256 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA18965 | hp2 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA18966 | hp1 | a0001 | c0004 | t0001 | g0005 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA18966 | hp2 | a0002 | c0001 | t0001 | g0249 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA18968 | hp1 | a0002 | c0001 | t0001 | g0225 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA18968 | hp2 | a0001 | c0004 | t0001 | g0120 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA18969 | hp1 | a0001 | c0004 | t0001 | g0102 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA18969 | hp2 | a0001 | c0002 | t0001 | g0268 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA18970 | hp1 | a0001 | c0002 | t0001 | g0265 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA18970 | hp2 | a0002 | c0001 | t0001 | g0206 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA18971 | hp1 | a0001 | c0004 | t0001 | g0116 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA18971 | hp2 | a0002 | c0001 | t0001 | g0200 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA18972 | hp1 | a0001 | c0002 | t0002 | g0302 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA18972 | hp2 | a0001 | c0004 | t0001 | g0127 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA18979 | hp1 | a0002 | c0001 | t0001 | g0276 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA18979 | hp2 | a0001 | c0004 | t0001 | g0158 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA18980 | hp1 | a0003 | c0003 | t0001 | g0060 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA18980 | hp2 | a0001 | c0004 | t0001 | g0030 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA18981 | hp1 | a0001 | c0004 | t0001 | g0122 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA18981 | hp2 | a0001 | c0002 | t0002 | g0024 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA18986 | hp1 | a0001 | c0004 | t0001 | g0118 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA18986 | hp2 | a0003 | c0003 | t0001 | g0075 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA18987 | hp1 | a0002 | c0001 | t0001 | g0019 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA18987 | hp2 | a0003 | c0016 | t0001 | g0100 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA18990 | hp1 | a0001 | c0004 | t0001 | g0143 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA18990 | hp2 | a0002 | c0001 | t0001 | g0018 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA18991 | hp1 | a0003 | c0003 | t0001 | g0081 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA18991 | hp2 | a0001 | c0017 | t0006 | g0138 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA18992 | hp1 | a0001 | c0004 | t0001 | g0156 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA18992 | hp2 | a0003 | c0003 | t0001 | g0047 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA18993 | hp1 | a0002 | c0001 | t0001 | g0250 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA18993 | hp2 | a0001 | c0004 | t0001 | g0105 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA18994 | hp1 | a0001 | c0004 | t0001 | g0032 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA18994 | hp2 | a0003 | c0003 | t0001 | g0098 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA18997 | hp1 | a0003 | c0003 | t0001 | g0093 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA18997 | hp2 | a0002 | c0001 | t0001 | g0212 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA18999 | hp1 | a0001 | c0002 | t0001 | g0267 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA18999 | hp2 | a0002 | c0001 | t0001 | g0018 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA19001 | hp1 | a0002 | c0001 | t0001 | g0235 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA19001 | hp2 | a0003 | c0003 | t0001 | g0095 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA19002 | hp1 | a0001 | c0002 | t0002 | g0316 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA19002 | hp2 | a0002 | c0001 | t0001 | g0273 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA19003 | hp1 | a0001 | c0004 | t0001 | g0112 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA19003 | hp2 | a0001 | c0002 | t0002 | g0289 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA19004 | hp1 | a0001 | c0004 | t0001 | g0119 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA19004 | hp2 | a0003 | c0014 | t0001 | g0074 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA19006 | hp1 | a0002 | c0001 | t0001 | g0260 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA19006 | hp2 | a0003 | c0003 | t0001 | g0051 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA19007 | hp1 | a0003 | c0003 | t0001 | g0068 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA19007 | hp2 | a0001 | c0002 | t0001 | g0266 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA19010 | hp1 | a0001 | c0002 | t0002 | g0024 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA19010 | hp2 | a0002 | c0001 | t0001 | g0237 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA19011 | hp1 | a0002 | c0001 | t0001 | g0020 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA19011 | hp2 | a0001 | c0004 | t0001 | g0031 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA19012 | hp1 | a0002 | c0001 | t0001 | g0255 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA19012 | hp2 | a0003 | c0003 | t0001 | g0055 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA19030 | hp1 | a0002 | c0012 | t0001 | g0042 | AFR | LWK | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA19030 | hp2 | a0001 | c0002 | t0002 | g0270 | AFR | LWK | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA19043 | hp1 | a0001 | c0002 | t0002 | g0294 | AFR | LWK | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA19043 | hp2 | a0001 | c0006 | t0001 | g0108 | AFR | LWK | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA19055 | hp1 | a0001 | c0004 | t0001 | g0002 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA19055 | hp2 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA19056 | hp1 | a0002 | c0001 | t0001 | g0229 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA19056 | hp2 | a0001 | c0004 | t0001 | g0148 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA19057 | hp1 | a0002 | c0001 | t0001 | g0050 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA19057 | hp2 | a0001 | c0004 | t0001 | g0144 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA19062 | hp1 | a0001 | c0004 | t0001 | g0036 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA19062 | hp2 | a0002 | c0001 | t0001 | g0277 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA19063 | hp1 | a0002 | c0001 | t0001 | g0187 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA19063 | hp2 | a0003 | c0003 | t0001 | g0049 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA19066 | hp1 | a0001 | c0002 | t0002 | g0284 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA19066 | hp2 | a0001 | c0004 | t0001 | g0152 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA19068 | hp1 | a0002 | c0001 | t0001 | g0019 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA19068 | hp2 | a0001 | c0002 | t0002 | g0303 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA19077 | hp1 | a0002 | c0001 | t0001 | g0251 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA19077 | hp2 | a0003 | c0003 | t0001 | g0091 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA19080 | hp1 | a0002 | c0001 | t0001 | g0247 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA19080 | hp2 | a0001 | c0004 | t0001 | g0002 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA19082 | hp1 | a0003 | c0003 | t0001 | g0007 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA19082 | hp2 | a0002 | c0001 | t0001 | g0190 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA19085 | hp1 | a0001 | c0004 | t0001 | g0106 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA19085 | hp2 | a0001 | c0004 | t0002 | g0037 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA19086 | hp1 | a0001 | c0004 | t0001 | g0140 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA19086 | hp2 | a0002 | c0001 | t0001 | g0211 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA19087 | hp1 | a0003 | c0003 | t0001 | g0065 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA19087 | hp2 | a0001 | c0004 | t0001 | g0014 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA19088 | hp1 | a0002 | c0001 | t0001 | g0257 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA19088 | hp2 | a0003 | c0003 | t0001 | g0007 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA19089 | hp1 | a0002 | c0001 | t0001 | g0201 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA19089 | hp2 | a0003 | c0003 | t0001 | g0079 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA19090 | hp1 | a0001 | c0004 | t0001 | g0150 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA19090 | hp2 | a0003 | c0003 | t0001 | g0099 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA19091 | hp1 | a0002 | c0001 | t0001 | g0218 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA19091 | hp2 | a0001 | c0004 | t0001 | g0015 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA19240 | hp1 | a0001 | c0006 | t0001 | g0101 | AFR | YRI | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA19240 | hp2 | a0003 | c0003 | t0001 | g0064 | AFR | YRI | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA20752 | hp1 | a0003 | c0003 | t0001 | g0011 | EUR | TSI | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA20752 | hp2 | a0002 | c0001 | t0001 | g0208 | EUR | TSI | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA20805 | hp1 | a0003 | c0003 | t0001 | g0012 | EUR | TSI | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA20805 | hp2 | a0002 | c0001 | t0001 | g0223 | EUR | TSI | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA20905 | hp1 | a0001 | c0002 | t0002 | g0304 | SAS | GIH | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA20905 | hp2 | a0001 | c0002 | t0002 | g0291 | SAS | GIH | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG01123 | hp1 | a0002 | c0001 | t0001 | g0021 | AMR | CLM | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG01123 | hp2 | a0003 | c0003 | t0001 | g0001 | AMR | CLM | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02109 | hp1 | a0001 | c0008 | t0001 | g0176 | AFR | ACB | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02109 | hp2 | a0003 | c0003 | t0001 | g0012 | AFR | ACB | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02486 | hp1 | a0001 | c0002 | t0002 | g0185 | AFR | ACB | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02486 | hp2 | a0001 | c0008 | t0001 | g0180 | AFR | ACB | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02559 | hp1 | a0001 | c0008 | t0001 | g0182 | AFR | ACB | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG02559 | hp2 | a0003 | c0003 | t0001 | g0072 | AFR | ACB | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG06807 | hp1 | a0001 | c0008 | t0001 | g0178 | AFR | USA | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
HG06807 | hp2 | a0003 | c0003 | t0001 | g0083 | AFR | USA | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA18955 | hp1 | a0001 | c0004 | t0001 | g0133 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA18955 | hp2 | a0002 | c0001 | t0001 | g0275 | EAS | JPT | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA20300 | hp1 | a0003 | c0003 | t0001 | g0111 | AFR | USA | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA20300 | hp2 | a0002 | c0011 | t0001 | g0035 | AFR | USA | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA21309 | hp1 | a0001 | c0009 | t0001 | g0052 | AFR | LWK | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
NA21309 | hp2 | a0001 | c0002 | t0001 | g0188 | AFR | LWK | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
homoSapiens_chm13v2 | hp1 | a0002 | c0001 | t0001 | g0222 | REF | REF | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
homoSapiens_grch38 | hp1 | a0003 | c0003 | t0001 | g0086 | REF | REF | SAMM50_chr22_43950442_44001529 | SAMM50 | chr22 | 43950442 | 44001529 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:43972242
|
A | G | 2 | a0002a0005 | 101 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(98): Show |
missense_variant | MODERATE | c.329A>G | p.Asp110Gly | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 5/15 | 465/1692 | 329/1410 | 110/469 | chr22 | 43972242 | ||
chr22:43972953
|
C | T | 1 | a0005 | 1 | HG03654.hp2 | missense_variant | MODERATE | c.512C>T | p.Ser171Leu | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 6/15 | 648/1692 | 512/1410 | 171/469 | chr22 | 43972953 | ||
chr22:43976772
|
G | A | 1 | a0004 | 1 | HG00438.hp1 | missense_variant | MODERATE | c.800G>A | p.Arg267Gln | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 9/15 | 936/1692 | 800/1410 | 267/469 | chr22 | 43976772 | ||
chr22:43983958
|
A | G | 3 | a0001a0002a0005 | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(296): Show |
missense_variant | MODERATE | c.1033A>G | p.Ile345Val | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/15 | 1169/1692 | 1033/1410 | 345/469 | chr22 | 43983958 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:43963366
|
A | G | 1 | a0001c0020 | 1 | HG03098.hp2 | synonymous_variant | LOW | c.102A>G | p.Glu34Glu | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 2/15 | 238/1692 | 102/1410 | 34/469 | chr22 | 43963366 | ||
chr22:43972324
|
A | G | 10 | a0001c0002a0001c0004a0001c0006others(7): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(268): Show |
synonymous_variant | LOW | c.411A>G | p.Gly137Gly | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 5/15 | 547/1692 | 411/1410 | 137/469 | chr22 | 43972324 | ||
chr22:43973296
|
G | A | 1 | a0001c0008 | 9 | HG01109.hp2 HG02109.hp1 HG02257.hp1 others(6): Show |
synonymous_variant | LOW | c.621G>A | p.Thr207Thr | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/15 | 757/1692 | 621/1410 | 207/469 | chr22 | 43973296 | ||
chr22:43976752
|
C | T | 5 | a0001c0002a0001c0008a0002c0001others(2): Show | 181 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(178): Show |
splice_region_variant&synonymous_variant | LOW | c.780C>T | p.His260His | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 9/15 | 916/1692 | 780/1410 | 260/469 | chr22 | 43976752 | ||
chr22:43983942
|
T | C | 13 | a0001c0002a0001c0004a0001c0006others(10): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(280): Show |
synonymous_variant | LOW | c.1017T>C | p.Leu339Leu | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/15 | 1153/1692 | 1017/1410 | 339/469 | chr22 | 43983942 | ||
chr22:43989148
|
C | T | 1 | a0001c0017 | 1 | NA18991.hp2 | synonymous_variant | LOW | c.1113C>T | p.Gly371Gly | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 13/15 | 1249/1692 | 1113/1410 | 371/469 | chr22 | 43989148 | ||
chr22:43989229
|
C | T | 1 | a0001c0010 | 3 | HG02615.hp1 HG02895.hp1 NA18522.hp2 |
synonymous_variant | LOW | c.1194C>T | p.Asn398Asn | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 13/15 | 1330/1692 | 1194/1410 | 398/469 | chr22 | 43989229 | ||
chr22:43990401
|
C | T | 7 | a0001c0004a0001c0005a0001c0013others(4): Show | 90 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(87): Show |
synonymous_variant | LOW | c.1359C>T | p.Gly453Gly | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/15 | 1495/1692 | 1359/1410 | 453/469 | chr22 | 43990401 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:43955453
|
T | C | 1 | a0001c0007t0003 | 1 | HG02809.hp2 | 5_prime_UTR_variant | MODIFIER | c.-125T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/15 | 125 | chr22 | 43955453 | |||||
chr22:43955456
|
G | T | 1 | a0005c0019t0007 | 1 | HG03654.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-122G>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/15 | chr22 | 43955456 | ||||||
chr22:43955471
|
T | C | 3 | a0001c0002t0002a0001c0002t0004a0001c0004t0002 | 55 | HG00099.hp2 HG00544.hp1 HG00558.hp1 others(52): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-107T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/15 | chr22 | 43955471 | ||||||
chr22:43996435
|
A | C | 1 | a0001c0017t0006 | 1 | NA18991.hp2 | 3_prime_UTR_variant | MODIFIER | c.*52A>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 15/15 | 52 | chr22 | 43996435 | |||||
chr22:43996453
|
C | T | 2 | a0001c0002t0004a0001c0007t0005 | 2 | HG03195.hp1 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*70C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 15/15 | 70 | chr22 | 43996453 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:43955691
|
G | T | 3 | a0001c0002t0001g0337a0001c0002t0001g0338a0001c0002t0001g0339 | 3 | HG02647.hp1 HG02965.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.21+93G>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43955691 | ||||||
chr22:43955966
|
A | G | 1 | a0001c0002t0002g0336 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.21+368A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43955966 | ||||||
chr22:43956261
|
G | A | 3 | a0001c0004t0001g0030a0001c0004t0001g0031a0001c0004t0001g0032 | 3 | NA18980.hp2 NA18994.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.21+663G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43956261 | ||||||
chr22:43956367
|
T | C | 1 | a0001c0008t0001g0033 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.21+769T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43956367 | ||||||
chr22:43956633
|
C | T | 11 | a0001c0005t0001g0029a0001c0005t0001g0328a0001c0005t0001g0329others(8): Show | 12 | HG02055.hp2 HG02280.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.21+1035C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43956633 | ||||||
chr22:43956710
|
G | A | 1 | a0001c0007t0005g0034 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.21+1112G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43956710 | ||||||
chr22:43956797
|
T | C | 1 | a0002c0011t0001g0035 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.21+1199T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43956797 | ||||||
chr22:43956917
|
G | A | 2 | a0001c0004t0001g0036a0001c0004t0002g0037 | 2 | NA19062.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.21+1319G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43956917 | ||||||
chr22:43956986
|
C | T | 3 | a0003c0003t0001g0003a0003c0003t0001g0324a0003c0003t0001g0325 | 6 | HG00140.hp1 HG00733.hp1 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.21+1388C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43956986 | ||||||
chr22:43957185
|
T | C | 2 | a0002c0001t0001g0038a0002c0001t0001g0039 | 2 | HG01243.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.21+1587T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43957185 | ||||||
chr22:43957374
|
G | C | 1 | a0001c0002t0002g0040 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.21+1776G>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43957374 | ||||||
chr22:43957567
|
C | T | 8 | a0001c0007t0001g0027a0001c0007t0001g0028a0001c0007t0001g0322others(5): Show | 10 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.21+1969C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43957567 | ||||||
chr22:43957616
|
G | A | 1 | a0001c0004t0001g0041 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.21+2018G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43957616 | ||||||
chr22:43957760
|
A | G | 3 | a0001c0007t0001g0028a0001c0007t0001g0322a0001c0007t0001g0323 | 4 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(1): Show |
intron_variant | MODIFIER | c.21+2162A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43957760 | ||||||
chr22:43957766
|
T | G | 3 | a0001c0006t0001g0043a0001c0006t0001g0044a0002c0012t0001g0042 | 3 | HG02451.hp1 HG03098.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.21+2168T>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43957766 | ||||||
chr22:43958004
|
C | T | 2 | a0001c0004t0001g0317a0001c0004t0001g0318 | 2 | HG02602.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.21+2406C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43958004 | ||||||
chr22:43958231
|
C | T | 150 | a0001c0002t0001g0022a0001c0002t0001g0188a0001c0002t0001g0189others(147): Show | 162 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.21+2633C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43958231 | ||||||
chr22:43958412
|
A | G | 1 | a0001c0013t0001g0321 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.21+2814A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43958412 | ||||||
chr22:43958421
|
G | A | 1 | a0001c0004t0001g0045 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.21+2823G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43958421 | ||||||
chr22:43958476
|
C | CT | 16 | a0001c0004t0001g0102a0001c0004t0001g0105a0001c0004t0001g0106others(13): Show | 16 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.21+2898dupT | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 43958476 | |||||
chr22:43958476
|
C | CTT | 69 | a0001c0002t0001g0188a0001c0004t0001g0002a0001c0004t0001g0005others(66): Show | 77 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.21+2897_21+2898dup others(2): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 43958476 | |||||
chr22:43958476
|
C | CTTT | 106 | a0001c0002t0001g0016a0001c0002t0001g0161a0001c0002t0001g0162others(103): Show | 114 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.21+2896_21+2898dup others(3): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 43958476 | |||||
chr22:43958476
|
C | CTTTT | 22 | a0001c0002t0001g0022a0001c0002t0001g0265a0001c0002t0001g0266others(19): Show | 24 | HG02155.hp1 HG02258.hp2 HG02559.hp1 others(21): Show |
intron_variant | MODIFIER | c.21+2895_21+2898dup others(4): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 43958476 | |||||
chr22:43958476
|
C | CTTTTT | 40 | a0001c0002t0001g0281a0001c0002t0002g0024a0001c0002t0002g0025others(37): Show | 43 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.21+2894_21+2898dup others(5): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 43958476 | |||||
chr22:43958476
|
CT | C | 6 | a0001c0007t0005g0034a0003c0003t0001g0007a0003c0003t0001g0046others(3): Show | 7 | HG00558.hp2 HG02451.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.21+2898delT | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 43958476 | |||||
chr22:43958518
|
A | G | 258 | a0001c0002t0001g0016a0001c0002t0001g0022a0001c0002t0001g0161others(255): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.21+2920A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43958518 | ||||||
chr22:43958718
|
C | T | 8 | a0001c0007t0001g0027a0001c0007t0001g0028a0001c0007t0001g0322others(5): Show | 10 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.21+3120C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43958718 | ||||||
chr22:43958743
|
C | T | 9 | a0001c0008t0001g0033a0001c0008t0001g0175a0001c0008t0001g0176others(6): Show | 9 | HG01109.hp2 HG02109.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.21+3145C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43958743 | ||||||
chr22:43958880
|
G | C | 1 | a0002c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.21+3282G>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43958880 | ||||||
chr22:43958961
|
C | T | 9 | a0001c0005t0001g0029a0001c0005t0001g0328a0001c0005t0001g0329others(6): Show | 10 | HG02055.hp2 HG02280.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.21+3363C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43958961 | ||||||
chr22:43958985
|
A | G | 82 | a0001c0004t0001g0002a0001c0004t0001g0005a0001c0004t0001g0013others(79): Show | 90 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.21+3387A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43958985 | ||||||
chr22:43959018
|
C | CT | 13 | a0001c0007t0001g0027a0001c0007t0001g0028a0001c0007t0001g0322others(10): Show | 15 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.21+3438dupT | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 43959018 | |||||
chr22:43959018
|
CT | C | 221 | a0001c0002t0001g0016a0001c0002t0001g0162a0001c0002t0001g0163others(218): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.21+3438delT | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 43959018 | |||||
chr22:43959018
|
CTT | C | 16 | a0001c0002t0001g0022a0001c0002t0001g0161a0001c0002t0001g0189others(13): Show | 17 | HG00323.hp1 HG00423.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.21+3437_21+3438del others(2): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 43959018 | |||||
chr22:43959270
|
C | T | 1 | a0001c0004t0001g0159 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.21+3672C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43959270 | ||||||
chr22:43959284
|
G | A | 1 | a0001c0002t0001g0189 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.21+3686G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43959284 | ||||||
chr22:43959350
|
A | G | 251 | a0001c0002t0001g0016a0001c0002t0001g0022a0001c0002t0001g0161others(248): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(269): Show |
intron_variant | MODIFIER | c.21+3752A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43959350 | ||||||
chr22:43959465
|
G | C | 1 | a0001c0007t0003g0320 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.22-3821G>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43959465 | ||||||
chr22:43959507
|
T | TAC | 37 | a0001c0020t0001g0327a0002c0001t0001g0259a0002c0001t0001g0260others(34): Show | 42 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.22-3744_22-3743dup others(2): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 43959507 | |||||
chr22:43959507
|
T | TACAC | 32 | a0001c0002t0001g0161a0001c0002t0001g0188a0001c0002t0001g0269others(29): Show | 36 | HG00558.hp1 HG00609.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.22-3746_22-3743dup others(4): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 43959507 | |||||
chr22:43959507
|
T | TACACAC | 86 | a0001c0002t0001g0022a0001c0002t0001g0189a0001c0002t0001g0265others(83): Show | 95 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.22-3748_22-3743dup others(6): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 43959507 | |||||
chr22:43959507
|
T | TACACACA others(1): Show |
38 | a0001c0002t0002g0185a0001c0002t0002g0274a0001c0002t0002g0298others(35): Show | 39 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(36): Show |
intron_variant | MODIFIER | c.22-3750_22-3743dup others(8): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 43959507 | |||||
chr22:43959507
|
T | TACACACA others(3): Show |
40 | a0001c0002t0002g0024a0001c0002t0002g0025a0001c0002t0002g0026others(37): Show | 45 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.22-3752_22-3743dup others(10): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 43959507 | |||||
chr22:43959507
|
T | TACACACA others(5): Show |
39 | a0001c0002t0001g0337a0001c0002t0001g0338a0001c0002t0001g0339others(36): Show | 45 | HG00609.hp1 HG00735.hp1 HG01169.hp2 others(42): Show |
intron_variant | MODIFIER | c.22-3754_22-3743dup others(12): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 43959507 | |||||
chr22:43959507
|
T | TACACACA others(7): Show |
30 | a0001c0002t0002g0023a0001c0002t0002g0040a0001c0002t0002g0183others(27): Show | 33 | HG00423.hp2 HG00738.hp2 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.22-3756_22-3743dup others(14): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 43959507 | |||||
chr22:43959507
|
T | TACACACA others(9): Show |
8 | a0001c0004t0001g0118a0001c0004t0001g0119a0001c0004t0001g0120others(5): Show | 8 | HG01070.hp2 HG01071.hp1 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.22-3758_22-3743dup others(16): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 43959507 | |||||
chr22:43959507
|
T | TACACACA others(11): Show |
3 | a0001c0004t0001g0036a0001c0004t0001g0116a0001c0004t0001g0117 | 3 | HG01496.hp1 NA18971.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.22-3760_22-3743dup others(18): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 43959507 | |||||
chr22:43959507
|
T | TACACACA others(13): Show |
1 | a0001c0004t0001g0115 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.22-3762_22-3743dup others(20): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 43959507 | |||||
chr22:43959507
|
TAC | T | 7 | a0001c0002t0001g0163a0001c0002t0001g0164a0003c0003t0001g0089others(4): Show | 7 | HG01081.hp1 HG02015.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.22-3744_22-3743del others(2): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 43959507 | |||||
chr22:43959507
|
TACAC | T | 5 | a0001c0002t0001g0016a0001c0002t0001g0165a0001c0002t0001g0166others(2): Show | 6 | HG01891.hp1 HG01934.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.22-3746_22-3743del others(4): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 43959507 | |||||
chr22:43959689
|
C | T | 71 | a0001c0004t0001g0002a0001c0004t0001g0005a0001c0004t0001g0013others(68): Show | 79 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.22-3597C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43959689 | ||||||
chr22:43959739
|
T | A | 1 | a0002c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.22-3547T>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43959739 | ||||||
chr22:43959847
|
T | G | 1 | a0002c0001t0001g0205 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.22-3439T>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43959847 | ||||||
chr22:43959902
|
A | C | 6 | a0001c0002t0001g0022a0001c0002t0001g0265a0001c0002t0001g0266others(3): Show | 7 | HG00423.hp1 NA18963.hp2 NA18965.hp2 others(4): Show |
intron_variant | MODIFIER | c.22-3384A>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43959902 | ||||||
chr22:43960007
|
C | T | 1 | a0001c0002t0001g0188 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.22-3279C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43960007 | ||||||
chr22:43960105
|
G | T | 2 | a0001c0009t0001g0052a0001c0009t0001g0053 | 2 | HG01433.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.22-3181G>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43960105 | ||||||
chr22:43960116
|
G | A | 2 | a0001c0002t0002g0024a0001c0002t0002g0308 | 3 | NA18939.hp1 NA18981.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.22-3170G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43960116 | ||||||
chr22:43960265
|
A | T | 1 | a0001c0002t0001g0189 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.22-3021A>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43960265 | ||||||
chr22:43960416
|
G | A | 3 | a0001c0004t0001g0132a0001c0004t0001g0143a0001c0004t0001g0160 | 3 | NA18953.hp2 NA18959.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.22-2870G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43960416 | ||||||
chr22:43960469
|
C | G | 81 | a0001c0004t0001g0002a0001c0004t0001g0005a0001c0004t0001g0013others(78): Show | 89 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.22-2817C>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43960469 | ||||||
chr22:43960588
|
G | A | 90 | a0002c0001t0001g0006a0002c0001t0001g0017a0002c0001t0001g0018others(87): Show | 97 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.22-2698G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43960588 | ||||||
chr22:43960600
|
G | T | 49 | a0001c0002t0002g0023a0001c0002t0002g0024a0001c0002t0002g0025others(46): Show | 53 | HG00099.hp2 HG00544.hp1 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.22-2686G>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43960600 | ||||||
chr22:43960682
|
T | C | 5 | a0001c0007t0001g0027a0001c0007t0001g0028a0001c0007t0001g0322others(2): Show | 7 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(4): Show |
intron_variant | MODIFIER | c.22-2604T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43960682 | ||||||
chr22:43960686
|
G | A | 72 | a0001c0004t0001g0002a0001c0004t0001g0005a0001c0004t0001g0013others(69): Show | 80 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.22-2600G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43960686 | ||||||
chr22:43960773
|
C | T | 3 | a0001c0006t0001g0043a0001c0006t0001g0044a0002c0012t0001g0042 | 3 | HG02451.hp1 HG03098.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.22-2513C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43960773 | ||||||
chr22:43961284
|
C | T | 3 | a0001c0006t0001g0043a0001c0006t0001g0044a0002c0012t0001g0042 | 3 | HG02451.hp1 HG03098.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.22-2002C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43961284 | ||||||
chr22:43961293
|
C | G | 1 | a0003c0003t0001g0083 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.22-1993C>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43961293 | ||||||
chr22:43961294
|
CT | C | 5 | a0001c0002t0002g0023a0001c0002t0002g0040a0001c0002t0002g0270others(2): Show | 6 | HG02258.hp2 HG02717.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.22-1990delT | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 43961294 | |||||
chr22:43961332
|
G | A | 1 | a0001c0007t0005g0034 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.22-1954G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43961332 | ||||||
chr22:43962014
|
G | T | 149 | a0001c0002t0001g0022a0001c0002t0001g0188a0001c0002t0001g0189others(146): Show | 161 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.22-1272G>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43962014 | ||||||
chr22:43962020
|
G | A | 257 | a0001c0002t0001g0016a0001c0002t0001g0022a0001c0002t0001g0161others(254): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.22-1266G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43962020 | ||||||
chr22:43962021
|
A | G | 1 | a0001c0002t0001g0168 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.22-1265A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43962021 | ||||||
chr22:43962048
|
A | C | 8 | a0001c0007t0001g0027a0001c0007t0001g0028a0001c0007t0001g0322others(5): Show | 10 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.22-1238A>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43962048 | ||||||
chr22:43962048
|
A | G | 4 | a0001c0008t0001g0175a0001c0008t0001g0178a0001c0008t0001g0181others(1): Show | 4 | HG02559.hp1 HG03041.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.22-1238A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43962048 | ||||||
chr22:43962060
|
T | A | 4 | a0001c0007t0001g0027a0001c0007t0001g0028a0001c0007t0001g0322others(1): Show | 6 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.22-1226T>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43962060 | ||||||
chr22:43962150
|
C | T | 8 | a0001c0007t0001g0027a0001c0007t0001g0028a0001c0007t0001g0322others(5): Show | 10 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.22-1136C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43962150 | ||||||
chr22:43962159
|
G | A | 1 | a0002c0001t0001g0207 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.22-1127G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43962159 | ||||||
chr22:43962160
|
A | C | 7 | a0001c0006t0001g0101a0001c0006t0001g0103a0001c0006t0001g0104others(4): Show | 7 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.22-1126A>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43962160 | ||||||
chr22:43962328
|
T | C | 2 | a0001c0013t0001g0319a0001c0013t0001g0321 | 2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.22-958T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43962328 | ||||||
chr22:43962356
|
G | A | 1 | a0001c0002t0002g0284 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.22-930G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43962356 | ||||||
chr22:43962356
|
G | T | 9 | a0001c0006t0001g0043a0001c0006t0001g0044a0001c0006t0001g0101others(6): Show | 9 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.22-930G>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43962356 | ||||||
chr22:43962386
|
C | G | 1 | a0001c0007t0003g0320 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.22-900C>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43962386 | ||||||
chr22:43962480
|
C | G | 7 | a0001c0007t0001g0027a0001c0007t0001g0028a0001c0007t0001g0322others(4): Show | 9 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.22-806C>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43962480 | ||||||
chr22:43962881
|
A | AT | 47 | a0001c0002t0001g0265a0001c0002t0001g0266a0001c0002t0001g0267others(44): Show | 49 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.22-372dupT | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 43962881 | |||||
chr22:43962881
|
A | ATT | 13 | a0001c0002t0001g0022a0001c0004t0001g0122a0001c0004t0001g0154others(10): Show | 15 | HG01175.hp2 HG01433.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.22-373_22-372dupTT | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 43962881 | |||||
chr22:43962881
|
A | ATTT | 7 | a0001c0008t0001g0033a0001c0008t0001g0179a0001c0009t0001g0052others(4): Show | 7 | HG02027.hp2 HG02145.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.22-374_22-372dupTT others(1): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 43962881 | |||||
chr22:43962881
|
A | ATTTT | 8 | a0001c0002t0001g0337a0001c0002t0001g0338a0001c0002t0001g0339others(5): Show | 8 | HG00140.hp2 HG00323.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.22-375_22-372dupTT others(2): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 43962881 | |||||
chr22:43962881
|
A | ATTTTT | 40 | a0001c0002t0001g0188a0001c0008t0001g0178a0001c0008t0001g0181others(37): Show | 42 | HG00408.hp2 HG00609.hp2 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.22-376_22-372dupTT others(3): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 43962881 | |||||
chr22:43962881
|
A | ATTTTTT | 22 | a0001c0008t0001g0175a0002c0001t0001g0020a0002c0001t0001g0202others(19): Show | 23 | HG01257.hp2 HG01361.hp1 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.22-377_22-372dupTT others(4): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 43962881 | |||||
chr22:43962881
|
A | ATTTTTTT others(1): Show |
7 | a0002c0001t0001g0187a0002c0001t0001g0203a0002c0001t0001g0240others(4): Show | 7 | HG01255.hp1 HG02056.hp2 HG02129.hp1 others(4): Show |
intron_variant | MODIFIER | c.22-379_22-372dupTT others(6): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 43962881 | |||||
chr22:43962881
|
A | ATTTTTTT others(3): Show |
1 | a0002c0001t0001g0196 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.22-381_22-372dupTT others(8): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 43962881 | |||||
chr22:43962881
|
A | ATTTTTTT others(6): Show |
2 | a0002c0001t0001g0021a0002c0001t0001g0258 | 3 | HG01123.hp1 HG01993.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.22-384_22-372dupTT others(11): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 43962881 | |||||
chr22:43962881
|
A | ATTTTTTT others(7): Show |
3 | a0002c0001t0001g0006a0002c0001t0001g0244a0002c0001t0001g0245 | 5 | HG01258.hp2 HG01952.hp1 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.22-385_22-372dupTT others(12): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 43962881 | |||||
chr22:43962881
|
A | ATTTTTTT others(8): Show |
1 | a0002c0001t0001g0204 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.22-386_22-372dupTT others(13): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 43962881 | |||||
chr22:43962881
|
A | ATTTTTTT others(12): Show |
1 | a0002c0001t0001g0246 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.22-390_22-372dupTT others(17): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 43962881 | |||||
chr22:43962881
|
AT | A | 43 | a0001c0002t0002g0023a0001c0002t0002g0025a0001c0002t0002g0026others(40): Show | 46 | HG00544.hp1 HG00735.hp2 HG01070.hp1 others(43): Show |
intron_variant | MODIFIER | c.22-372delT | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 43962881 | |||||
chr22:43962881
|
ATTTTTTT others(3): Show |
A | 1 | a0002c0001t0001g0208 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.22-381_22-372delTT others(8): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 43962881 | |||||
chr22:43962881
|
ATTTTTTT others(8): Show |
A | 3 | a0002c0001t0001g0191a0002c0001t0001g0193a0002c0001t0001g0194 | 3 | HG02572.hp2 HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.22-386_22-372delTT others(13): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 43962881 | |||||
chr22:43962881
|
ATTTTTTT others(9): Show |
A | 5 | a0001c0004t0001g0133a0001c0007t0001g0027a0001c0007t0001g0028others(2): Show | 7 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(4): Show |
intron_variant | MODIFIER | c.22-387_22-372delTT others(14): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 43962881 | |||||
chr22:43962881
|
ATTTTTTT others(10): Show |
A | 11 | a0001c0002t0001g0016a0001c0002t0001g0161a0001c0002t0001g0162others(8): Show | 12 | HG01109.hp2 HG01891.hp1 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.22-388_22-372delTT others(15): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 43962881 | |||||
chr22:43962882
|
T | A | 1 | a0001c0004t0001g0144 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.22-404T>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43962882 | ||||||
chr22:43962932
|
G | A | 74 | a0001c0002t0001g0337a0001c0002t0001g0338a0001c0004t0001g0002others(71): Show | 82 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.22-354G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43962932 | ||||||
chr22:43962939
|
G | C | 8 | a0001c0007t0001g0027a0001c0007t0001g0028a0001c0007t0001g0322others(5): Show | 10 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.22-347G>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43962939 | ||||||
chr22:43963117
|
A | G | 71 | a0002c0001t0001g0006a0002c0001t0001g0017a0002c0001t0001g0018others(68): Show | 78 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.22-169A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43963117 | ||||||
chr22:43963126
|
G | A | 1 | a0003c0003t0001g0088 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.22-160G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 1/14 | chr22 | 43963126 | ||||||
chr22:43963433
|
G | T | 2 | a0001c0006t0001g0043a0001c0006t0001g0044 | 2 | HG02451.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.132+37G>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 2/14 | chr22 | 43963433 | ||||||
chr22:43963771
|
T | C | 8 | a0001c0007t0001g0027a0001c0007t0001g0028a0001c0007t0001g0322others(5): Show | 10 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.132+375T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 2/14 | chr22 | 43963771 | ||||||
chr22:43963835
|
C | T | 43 | a0001c0002t0002g0024a0001c0002t0002g0025a0001c0002t0002g0026others(40): Show | 46 | HG00099.hp2 HG00544.hp1 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.132+439C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 2/14 | chr22 | 43963835 | ||||||
chr22:43963849
|
C | T | 8 | a0001c0007t0001g0027a0001c0007t0001g0028a0001c0007t0001g0322others(5): Show | 10 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.132+453C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 2/14 | chr22 | 43963849 | ||||||
chr22:43963865
|
C | A | 1 | a0001c0002t0002g0295 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.132+469C>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 2/14 | chr22 | 43963865 | ||||||
chr22:43963904
|
T | G | 2 | a0003c0003t0001g0007a0003c0003t0001g0046 | 3 | HG00558.hp2 NA19082.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.132+508T>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 2/14 | chr22 | 43963904 | ||||||
chr22:43963909
|
T | TTTTTTAT others(324): Show |
2 | a0001c0002t0001g0165a0001c0002t0001g0166 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.132+517_132+518ins others(331): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr22 | 43963909 | |||||
chr22:43963909
|
T | TTTTTTAT others(324): Show |
4 | a0001c0002t0001g0016a0001c0002t0001g0163a0001c0002t0001g0167others(1): Show | 5 | HG01891.hp1 HG01934.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.132+517_132+518ins others(331): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr22 | 43963909 | |||||
chr22:43963909
|
T | TTTTTTAT others(321): Show |
1 | a0001c0002t0001g0162 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.132+517_132+518ins others(328): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr22 | 43963909 | |||||
chr22:43963909
|
T | TTTTTTAT others(321): Show |
1 | a0001c0002t0001g0161 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.132+517_132+518ins others(328): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr22 | 43963909 | |||||
chr22:43963909
|
T | TTTTTTAT others(321): Show |
1 | a0001c0002t0001g0164 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.132+517_132+518ins others(328): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr22 | 43963909 | |||||
chr22:43963914
|
A | T | 9 | a0001c0002t0001g0016a0001c0002t0001g0161a0001c0002t0001g0162others(6): Show | 10 | HG01891.hp1 HG01934.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.132+518A>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 2/14 | chr22 | 43963914 | ||||||
chr22:43963918
|
T | A | 9 | a0001c0002t0001g0016a0001c0002t0001g0161a0001c0002t0001g0162others(6): Show | 10 | HG01891.hp1 HG01934.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.132+522T>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 2/14 | chr22 | 43963918 | ||||||
chr22:43963965
|
C | T | 2 | a0001c0009t0001g0052a0001c0009t0001g0053 | 2 | HG01433.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.133-487C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 2/14 | chr22 | 43963965 | ||||||
chr22:43964058
|
C | A | 4 | a0001c0007t0001g0027a0001c0007t0001g0028a0001c0007t0001g0322others(1): Show | 6 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.133-394C>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 2/14 | chr22 | 43964058 | ||||||
chr22:43964121
|
T | C | 2 | a0002c0011t0001g0035a0002c0011t0001g0248 | 2 | HG00639.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.133-331T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 2/14 | chr22 | 43964121 | ||||||
chr22:43964127
|
G | A | 71 | a0001c0004t0001g0002a0001c0004t0001g0005a0001c0004t0001g0013others(68): Show | 79 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.133-325G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 2/14 | chr22 | 43964127 | ||||||
chr22:43964130
|
C | A | 71 | a0001c0004t0001g0002a0001c0004t0001g0005a0001c0004t0001g0013others(68): Show | 79 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.133-322C>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 2/14 | chr22 | 43964130 | ||||||
chr22:43964176
|
C | A | 9 | a0001c0002t0001g0016a0001c0002t0001g0161a0001c0002t0001g0162others(6): Show | 10 | HG01891.hp1 HG01934.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.133-276C>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 2/14 | chr22 | 43964176 | ||||||
chr22:43964243
|
A | G | 2 | a0001c0002t0001g0165a0001c0002t0001g0166 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.133-209A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 2/14 | chr22 | 43964243 | ||||||
chr22:43964254
|
A | G | 9 | a0001c0008t0001g0033a0001c0008t0001g0175a0001c0008t0001g0176others(6): Show | 9 | HG01109.hp2 HG02109.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.133-198A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 2/14 | chr22 | 43964254 | ||||||
chr22:43964362
|
C | G | 1 | a0002c0001t0001g0245 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.133-90C>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 2/14 | chr22 | 43964362 | ||||||
chr22:43964611
|
G | A | 2 | a0001c0006t0001g0043a0001c0006t0001g0044 | 2 | HG02451.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.234+58G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43964611 | ||||||
chr22:43964656
|
C | T | 2 | a0001c0002t0002g0312a0001c0002t0002g0313 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.234+103C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43964656 | ||||||
chr22:43964862
|
G | A | 1 | a0001c0002t0001g0337 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.234+309G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43964862 | ||||||
chr22:43964875
|
G | C | 3 | a0001c0002t0001g0337a0001c0002t0001g0338a0001c0002t0001g0339 | 3 | HG02647.hp1 HG02965.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.234+322G>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43964875 | ||||||
chr22:43964936
|
G | A | 1 | a0003c0003t0001g0324 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.234+383G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43964936 | ||||||
chr22:43965005
|
G | C | 1 | a0002c0001t0001g0203 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.234+452G>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43965005 | ||||||
chr22:43965184
|
T | TA | 261 | a0001c0002t0001g0016a0001c0002t0001g0022a0001c0002t0001g0161others(258): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(280): Show |
intron_variant | MODIFIER | c.234+649dupA | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr22 | 43965184 | |||||
chr22:43965184
|
T | TAA | 8 | a0001c0002t0002g0289a0001c0002t0002g0336a0001c0004t0001g0105others(5): Show | 8 | HG01243.hp1 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.234+648_234+649dup others(2): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr22 | 43965184 | |||||
chr22:43965216
|
A | T | 1 | a0001c0007t0003g0320 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.234+663A>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43965216 | ||||||
chr22:43965264
|
G | A | 1 | a0002c0001t0001g0196 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.234+711G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43965264 | ||||||
chr22:43965617
|
C | A | 68 | a0001c0004t0001g0002a0001c0004t0001g0005a0001c0004t0001g0013others(65): Show | 76 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.234+1064C>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43965617 | ||||||
chr22:43965729
|
A | AT | 273 | a0001c0002t0001g0016a0001c0002t0001g0022a0001c0002t0001g0161others(270): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(294): Show |
intron_variant | MODIFIER | c.234+1185dupT | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr22 | 43965729 | |||||
chr22:43965833
|
T | A | 26 | a0001c0007t0001g0027a0001c0007t0001g0028a0001c0007t0001g0322others(23): Show | 29 | HG00280.hp2 HG00621.hp2 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.234+1280T>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43965833 | ||||||
chr22:43965869
|
G | A | 1 | a0001c0007t0001g0326 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.234+1316G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43965869 | ||||||
chr22:43965962
|
C | T | 97 | a0001c0002t0001g0188a0001c0002t0001g0337a0001c0002t0001g0338others(94): Show | 104 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.234+1409C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43965962 | ||||||
chr22:43966298
|
G | A | 8 | a0001c0007t0001g0027a0001c0007t0001g0028a0001c0007t0001g0322others(5): Show | 10 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.234+1745G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43966298 | ||||||
chr22:43966379
|
C | T | 1 | a0001c0013t0001g0321 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.234+1826C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43966379 | ||||||
chr22:43966383
|
G | C | 2 | a0003c0003t0001g0084a0003c0003t0001g0089 | 2 | HG00642.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.234+1830G>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43966383 | ||||||
chr22:43966388
|
G | A | 1 | a0002c0001t0001g0250 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.234+1835G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43966388 | ||||||
chr22:43966605
|
C | T | 1 | a0001c0005t0001g0155 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.234+2052C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43966605 | ||||||
chr22:43966652
|
G | A | 249 | a0001c0002t0001g0016a0001c0002t0001g0022a0001c0002t0001g0161others(246): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.235-2079G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43966652 | ||||||
chr22:43966743
|
G | A | 1 | a0002c0001t0001g0221 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.235-1988G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43966743 | ||||||
chr22:43966808
|
A | AT | 201 | a0001c0002t0001g0016a0001c0002t0001g0022a0001c0002t0001g0161others(198): Show | 215 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.235-1912dupT | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr22 | 43966808 | |||||
chr22:43966808
|
A | ATT | 69 | a0001c0004t0001g0002a0001c0004t0001g0005a0001c0004t0001g0013others(66): Show | 77 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.235-1913_235-1912d others(4): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr22 | 43966808 | |||||
chr22:43966907
|
A | G | 12 | a0001c0005t0001g0029a0001c0005t0001g0155a0001c0005t0001g0328others(9): Show | 13 | HG02055.hp2 HG02280.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.235-1824A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43966907 | ||||||
chr22:43966935
|
C | T | 76 | a0001c0004t0001g0002a0001c0004t0001g0005a0001c0004t0001g0013others(73): Show | 84 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.235-1796C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43966935 | ||||||
chr22:43966961
|
C | G | 7 | a0001c0006t0001g0101a0001c0006t0001g0103a0001c0006t0001g0104others(4): Show | 7 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.235-1770C>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43966961 | ||||||
chr22:43967138
|
A | G | 1 | a0001c0002t0004g0293 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.235-1593A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43967138 | ||||||
chr22:43967257
|
A | G | 1 | a0002c0001t0001g0243 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.235-1474A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43967257 | ||||||
chr22:43967463
|
T | G | 1 | a0001c0006t0001g0103 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.235-1268T>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43967463 | ||||||
chr22:43967585
|
C | T | 2 | a0001c0002t0002g0026a0001c0002t0002g0292 | 3 | HG00735.hp2 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.235-1146C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43967585 | ||||||
chr22:43967739
|
T | TC | 252 | a0001c0002t0001g0016a0001c0002t0001g0022a0001c0002t0001g0161others(249): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(270): Show |
intron_variant | MODIFIER | c.235-991dupC | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr22 | 43967739 | |||||
chr22:43967765
|
T | C | 1 | a0001c0004t0001g0141 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.235-966T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43967765 | ||||||
chr22:43967777
|
G | A | 1 | a0001c0004t0001g0135 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.235-954G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43967777 | ||||||
chr22:43967856
|
C | T | 8 | a0001c0007t0001g0027a0001c0007t0001g0028a0001c0007t0001g0322others(5): Show | 10 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.235-875C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43967856 | ||||||
chr22:43967915
|
A | C | 1 | a0001c0004t0001g0148 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.235-816A>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43967915 | ||||||
chr22:43967943
|
C | T | 3 | a0001c0002t0001g0016a0001c0002t0001g0163a0001c0002t0001g0167 | 4 | HG01891.hp1 HG01934.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.235-788C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43967943 | ||||||
chr22:43968059
|
T | A | 69 | a0001c0004t0001g0002a0001c0004t0001g0005a0001c0004t0001g0013others(66): Show | 77 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.235-672T>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43968059 | ||||||
chr22:43968104
|
G | A | 9 | a0001c0006t0001g0043a0001c0006t0001g0044a0001c0006t0001g0101others(6): Show | 9 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.235-627G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43968104 | ||||||
chr22:43968127
|
C | T | 1 | a0001c0006t0001g0264 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.235-604C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43968127 | ||||||
chr22:43968144
|
T | A | 3 | a0001c0007t0005g0034a0001c0013t0001g0319a0001c0013t0001g0321 | 3 | HG02723.hp2 HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.235-587T>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43968144 | ||||||
chr22:43968221
|
T | C | 2 | a0001c0004t0001g0113a0001c0004t0001g0128 | 2 | NA18949.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.235-510T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43968221 | ||||||
chr22:43968226
|
C | CA | 7 | a0001c0002t0001g0189a0001c0007t0005g0034a0001c0008t0001g0179others(4): Show | 7 | HG02257.hp1 HG02486.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.235-484dupA | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr22 | 43968226 | |||||
chr22:43968226
|
CA | C | 206 | a0001c0002t0001g0188a0001c0002t0001g0337a0001c0002t0001g0338others(203): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.235-484delA | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr22 | 43968226 | |||||
chr22:43968226
|
CAA | C | 7 | a0001c0002t0002g0313a0001c0004t0001g0114a0002c0001t0001g0205others(4): Show | 7 | HG00323.hp1 HG01515.hp1 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.235-485_235-484del others(2): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr22 | 43968226 | |||||
chr22:43968226
|
CAAAAAAA others(8): Show |
C | 11 | a0001c0002t0001g0016a0001c0002t0001g0161a0001c0002t0001g0162others(8): Show | 12 | HG01109.hp2 HG01891.hp1 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.235-498_235-484del others(15): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr22 | 43968226 | |||||
chr22:43968239
|
AAAAAAAA others(9): Show |
A | 4 | a0001c0008t0001g0175a0001c0008t0001g0178a0001c0008t0001g0181others(1): Show | 4 | HG02559.hp1 HG03041.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.235-484_235-469del others(16): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr22 | 43968239 | |||||
chr22:43968264
|
A | AAAAAAAA others(10): Show |
1 | a0001c0004t0001g0032 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.235-455_235-454ins others(17): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr22 | 43968264 | |||||
chr22:43968447
|
G | A | 3 | a0001c0008t0001g0033a0001c0008t0001g0179a0001c0008t0001g0180 | 3 | HG02257.hp1 HG02486.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.235-284G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43968447 | ||||||
chr22:43968487
|
C | T | 4 | a0001c0002t0002g0183a0001c0002t0002g0280a0001c0002t0002g0283others(1): Show | 4 | HG02258.hp1 HG02970.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.235-244C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43968487 | ||||||
chr22:43968534
|
G | A | 1 | a0003c0003t0001g0076 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.235-197G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43968534 | ||||||
chr22:43968615
|
T | G | 3 | a0001c0002t0001g0337a0001c0002t0001g0338a0001c0002t0001g0339 | 3 | HG02647.hp1 HG02965.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.235-116T>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43968615 | ||||||
chr22:43968677
|
T | C | 3 | a0001c0007t0005g0034a0001c0013t0001g0319a0001c0013t0001g0321 | 3 | HG02723.hp2 HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.235-54T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43968677 | ||||||
chr22:43968714
|
C | T | 256 | a0001c0002t0001g0016a0001c0002t0001g0022a0001c0002t0001g0161others(253): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.235-17C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43968714 | ||||||
chr22:43968716
|
T | C | 4 | a0001c0004t0001g0036a0001c0004t0001g0116a0001c0004t0001g0142others(1): Show | 4 | HG00735.hp1 NA18971.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.235-15T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 3/14 | chr22 | 43968716 | ||||||
chr22:43968828
|
G | T | 1 | a0001c0002t0001g0189 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.322+10G>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 4/14 | chr22 | 43968828 | ||||||
chr22:43968914
|
T | C | 258 | a0001c0002t0001g0016a0001c0002t0001g0022a0001c0002t0001g0161others(255): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.322+96T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 4/14 | chr22 | 43968914 | ||||||
chr22:43969187
|
C | G | 1 | a0002c0001t0001g0196 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.322+369C>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 4/14 | chr22 | 43969187 | ||||||
chr22:43969352
|
G | C | 259 | a0001c0002t0001g0016a0001c0002t0001g0022a0001c0002t0001g0161others(256): Show | 282 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.322+534G>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 4/14 | chr22 | 43969352 | ||||||
chr22:43969523
|
C | T | 1 | a0003c0014t0001g0074 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.322+705C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 4/14 | chr22 | 43969523 | ||||||
chr22:43969542
|
A | C | 1 | a0001c0002t0002g0291 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.322+724A>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 4/14 | chr22 | 43969542 | ||||||
chr22:43969635
|
C | T | 1 | a0003c0003t0001g0111 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.322+817C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 4/14 | chr22 | 43969635 | ||||||
chr22:43969808
|
T | G | 11 | a0001c0002t0001g0016a0001c0002t0001g0161a0001c0002t0001g0162others(8): Show | 12 | HG01109.hp2 HG01891.hp1 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.322+990T>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 4/14 | chr22 | 43969808 | ||||||
chr22:43969862
|
G | A | 251 | a0001c0002t0001g0016a0001c0002t0001g0022a0001c0002t0001g0161others(248): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(269): Show |
intron_variant | MODIFIER | c.322+1044G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 4/14 | chr22 | 43969862 | ||||||
chr22:43969899
|
T | A | 1 | a0002c0001t0001g0261 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.322+1081T>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 4/14 | chr22 | 43969899 | ||||||
chr22:43970101
|
C | T | 6 | a0001c0002t0001g0022a0001c0002t0001g0265a0001c0002t0001g0266others(3): Show | 7 | HG00423.hp1 NA18963.hp2 NA18965.hp2 others(4): Show |
intron_variant | MODIFIER | c.322+1283C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 4/14 | chr22 | 43970101 | ||||||
chr22:43970115
|
G | A | 1 | a0001c0002t0002g0285 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.322+1297G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 4/14 | chr22 | 43970115 | ||||||
chr22:43970137
|
C | T | 1 | a0001c0004t0001g0157 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.322+1319C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 4/14 | chr22 | 43970137 | ||||||
chr22:43970255
|
G | A | 8 | a0001c0007t0001g0027a0001c0007t0001g0028a0001c0007t0001g0322others(5): Show | 10 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.322+1437G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 4/14 | chr22 | 43970255 | ||||||
chr22:43970260
|
G | A | 2 | a0003c0003t0001g0055a0003c0003t0001g0068 | 2 | NA19007.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.322+1442G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 4/14 | chr22 | 43970260 | ||||||
chr22:43970454
|
G | A | 1 | a0001c0004t0001g0031 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.322+1636G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 4/14 | chr22 | 43970454 | ||||||
chr22:43970797
|
C | T | 11 | a0001c0002t0001g0016a0001c0002t0001g0161a0001c0002t0001g0162others(8): Show | 12 | HG01109.hp2 HG01891.hp1 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.323-1439C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 4/14 | chr22 | 43970797 | ||||||
chr22:43970818
|
A | G | 4 | a0001c0005t0001g0328a0001c0005t0001g0329a0001c0005t0001g0330others(1): Show | 4 | HG02615.hp2 HG02965.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.323-1418A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 4/14 | chr22 | 43970818 | ||||||
chr22:43970929
|
A | G | 261 | a0001c0002t0001g0016a0001c0002t0001g0022a0001c0002t0001g0161others(258): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.323-1307A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 4/14 | chr22 | 43970929 | ||||||
chr22:43970994
|
G | A | 7 | a0001c0002t0002g0302a0001c0002t0002g0303a0001c0002t0002g0316others(4): Show | 9 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.323-1242G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 4/14 | chr22 | 43970994 | ||||||
chr22:43971081
|
T | G | 3 | a0001c0002t0002g0026a0001c0002t0002g0292a0001c0002t0002g0296 | 4 | HG00735.hp2 HG01192.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.323-1155T>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 4/14 | chr22 | 43971081 | ||||||
chr22:43971184
|
C | T | 3 | a0001c0006t0001g0043a0001c0006t0001g0044a0002c0012t0001g0042 | 3 | HG02451.hp1 HG03098.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.323-1052C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 4/14 | chr22 | 43971184 | ||||||
chr22:43971322
|
C | T | 1 | a0002c0001t0001g0205 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.323-914C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 4/14 | chr22 | 43971322 | ||||||
chr22:43971323
|
G | T | 9 | a0001c0002t0001g0016a0001c0002t0001g0161a0001c0002t0001g0162others(6): Show | 10 | HG01891.hp1 HG01934.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.323-913G>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 4/14 | chr22 | 43971323 | ||||||
chr22:43971369
|
C | T | 58 | a0001c0002t0001g0022a0001c0002t0001g0189a0001c0002t0001g0265others(55): Show | 63 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.323-867C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 4/14 | chr22 | 43971369 | ||||||
chr22:43971538
|
G | A | 7 | a0001c0006t0001g0101a0001c0006t0001g0103a0001c0006t0001g0104others(4): Show | 7 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.323-698G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 4/14 | chr22 | 43971538 | ||||||
chr22:43971749
|
C | T | 3 | a0001c0007t0005g0034a0001c0013t0001g0319a0001c0013t0001g0321 | 3 | HG02723.hp2 HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.323-487C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 4/14 | chr22 | 43971749 | ||||||
chr22:43971943
|
C | T | 1 | a0001c0002t0002g0287 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.323-293C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 4/14 | chr22 | 43971943 | ||||||
chr22:43971992
|
CTCAGCCC others(3): Show |
C | 1 | a0001c0004t0001g0140 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.323-242_323-233del others(10): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr22 | 43971992 | |||||
chr22:43972159
|
T | C | 49 | a0001c0002t0002g0023a0001c0002t0002g0024a0001c0002t0002g0025others(46): Show | 53 | HG00099.hp2 HG00544.hp1 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.323-77T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 4/14 | chr22 | 43972159 | ||||||
chr22:43972493
|
C | T | 6 | a0001c0002t0001g0016a0001c0002t0001g0163a0001c0002t0001g0165others(3): Show | 7 | HG01891.hp1 HG01934.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.429+151C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 5/14 | chr22 | 43972493 | ||||||
chr22:43972704
|
G | A | 4 | a0001c0007t0001g0027a0001c0007t0001g0028a0001c0007t0001g0322others(1): Show | 6 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.430-167G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 5/14 | chr22 | 43972704 | ||||||
chr22:43972848
|
A | AT | 176 | a0001c0002t0001g0016a0001c0002t0001g0022a0001c0002t0001g0161others(173): Show | 189 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.430-11dupT | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr22 | 43972848 | |||||
chr22:43972861
|
C | T | 248 | a0001c0002t0001g0016a0001c0002t0001g0022a0001c0002t0001g0161others(245): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.430-10C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 5/14 | chr22 | 43972861 | ||||||
chr22:43973153
|
G | A | 1 | a0001c0002t0002g0284 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.561-83G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 6/14 | chr22 | 43973153 | ||||||
chr22:43973357
|
G | A | 9 | a0001c0002t0001g0016a0001c0002t0001g0161a0001c0002t0001g0162others(6): Show | 10 | HG01891.hp1 HG01934.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.648+34G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43973357 | ||||||
chr22:43973411
|
G | A | 5 | a0002c0001t0001g0018a0002c0001t0001g0206a0002c0001t0001g0210others(2): Show | 6 | HG00621.hp2 HG04184.hp2 NA18947.hp1 others(3): Show |
intron_variant | MODIFIER | c.648+88G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43973411 | ||||||
chr22:43973449
|
C | T | 152 | a0001c0002t0001g0022a0001c0002t0001g0188a0001c0002t0001g0189others(149): Show | 164 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.648+126C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43973449 | ||||||
chr22:43973500
|
G | T | 9 | a0001c0002t0001g0016a0001c0002t0001g0161a0001c0002t0001g0162others(6): Show | 10 | HG01891.hp1 HG01934.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.648+177G>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43973500 | ||||||
chr22:43973549
|
C | T | 256 | a0001c0002t0001g0016a0001c0002t0001g0022a0001c0002t0001g0161others(253): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.648+226C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43973549 | ||||||
chr22:43973748
|
G | A | 3 | a0001c0010t0001g0124a0001c0010t0001g0136a0001c0010t0001g0145 | 3 | HG02615.hp1 HG02895.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.648+425G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43973748 | ||||||
chr22:43973825
|
C | T | 1 | a0001c0007t0005g0034 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.648+502C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43973825 | ||||||
chr22:43973899
|
C | T | 9 | a0003c0003t0001g0049a0003c0003t0001g0062a0003c0003t0001g0073others(6): Show | 9 | HG00621.hp1 HG02145.hp1 NA18949.hp2 others(6): Show |
intron_variant | MODIFIER | c.648+576C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43973899 | ||||||
chr22:43974024
|
CT | C | 248 | a0001c0002t0001g0016a0001c0002t0001g0022a0001c0002t0001g0161others(245): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.648+712delT | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr22 | 43974024 | |||||
chr22:43974035
|
T | C | 3 | a0001c0002t0001g0337a0001c0002t0001g0338a0001c0002t0001g0339 | 3 | HG02647.hp1 HG02965.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.648+712T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43974035 | ||||||
chr22:43974047
|
C | T | 7 | a0001c0007t0001g0027a0001c0007t0001g0028a0001c0007t0001g0322others(4): Show | 9 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.648+724C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43974047 | ||||||
chr22:43974062
|
C | T | 3 | a0001c0007t0005g0034a0001c0013t0001g0319a0001c0013t0001g0321 | 3 | HG02723.hp2 HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.648+739C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43974062 | ||||||
chr22:43974266
|
C | G | 1 | a0002c0001t0001g0242 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.648+943C>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43974266 | ||||||
chr22:43974295
|
C | G | 1 | a0001c0004t0001g0140 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.648+972C>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43974295 | ||||||
chr22:43974295
|
C | T | 68 | a0001c0004t0001g0002a0001c0004t0001g0005a0001c0004t0001g0013others(65): Show | 76 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.648+972C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43974295 | ||||||
chr22:43974357
|
A | T | 1 | a0003c0003t0001g0054 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.648+1034A>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43974357 | ||||||
chr22:43974396
|
G | A | 4 | a0001c0008t0001g0175a0001c0008t0001g0178a0001c0008t0001g0181others(1): Show | 4 | HG02559.hp1 HG03041.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.648+1073G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43974396 | ||||||
chr22:43974456
|
T | G | 258 | a0001c0002t0001g0016a0001c0002t0001g0022a0001c0002t0001g0161others(255): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.648+1133T>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43974456 | ||||||
chr22:43974457
|
T | C | 258 | a0001c0002t0001g0016a0001c0002t0001g0022a0001c0002t0001g0161others(255): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.648+1134T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43974457 | ||||||
chr22:43974548
|
A | C | 2 | a0002c0011t0001g0035a0002c0011t0001g0248 | 2 | HG00639.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.648+1225A>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43974548 | ||||||
chr22:43974559
|
A | C | 7 | a0001c0007t0001g0027a0001c0007t0001g0028a0001c0007t0001g0322others(4): Show | 9 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.648+1236A>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43974559 | ||||||
chr22:43974735
|
T | C | 274 | a0001c0002t0001g0016a0001c0002t0001g0022a0001c0002t0001g0161others(271): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(295): Show |
intron_variant | MODIFIER | c.649-1320T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43974735 | ||||||
chr22:43974781
|
G | A | 2 | a0001c0004t0001g0115a0001c0004t0001g0130 | 2 | HG03927.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.649-1274G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43974781 | ||||||
chr22:43974786
|
C | T | 1 | a0001c0002t0002g0274 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.649-1269C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43974786 | ||||||
chr22:43974788
|
C | T | 7 | a0001c0006t0001g0101a0001c0006t0001g0103a0001c0006t0001g0104others(4): Show | 7 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.649-1267C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43974788 | ||||||
chr22:43975060
|
C | T | 1 | a0001c0004t0001g0142 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.649-995C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43975060 | ||||||
chr22:43975073
|
G | T | 1 | a0001c0002t0001g0188 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.649-982G>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43975073 | ||||||
chr22:43975075
|
A | G | 14 | a0001c0006t0001g0101a0001c0006t0001g0103a0001c0006t0001g0104others(11): Show | 16 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.649-980A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43975075 | ||||||
chr22:43975100
|
A | G | 1 | a0003c0003t0001g0111 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.649-955A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43975100 | ||||||
chr22:43975127
|
G | C | 4 | a0002c0001t0001g0240a0002c0001t0001g0258a0002c0012t0001g0149others(1): Show | 4 | HG00280.hp1 HG01255.hp1 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.649-928G>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43975127 | ||||||
chr22:43975150
|
G | A | 4 | a0001c0007t0001g0027a0001c0007t0001g0028a0001c0007t0001g0322others(1): Show | 6 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.649-905G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43975150 | ||||||
chr22:43975207
|
C | T | 1 | a0001c0004t0001g0142 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.649-848C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43975207 | ||||||
chr22:43975363
|
A | G | 247 | a0001c0002t0001g0016a0001c0002t0001g0022a0001c0002t0001g0161others(244): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.649-692A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43975363 | ||||||
chr22:43975408
|
C | A | 1 | a0001c0002t0002g0287 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.649-647C>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43975408 | ||||||
chr22:43975432
|
G | A | 247 | a0001c0002t0001g0016a0001c0002t0001g0022a0001c0002t0001g0161others(244): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.649-623G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43975432 | ||||||
chr22:43975446
|
A | C | 3 | a0001c0008t0001g0033a0001c0008t0001g0179a0001c0008t0001g0180 | 3 | HG02257.hp1 HG02486.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.649-609A>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43975446 | ||||||
chr22:43975502
|
G | C | 4 | a0001c0002t0001g0188a0001c0002t0001g0337a0001c0002t0001g0338others(1): Show | 4 | HG02647.hp1 HG02965.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.649-553G>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43975502 | ||||||
chr22:43975526
|
A | G | 90 | a0002c0001t0001g0006a0002c0001t0001g0017a0002c0001t0001g0018others(87): Show | 97 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.649-529A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43975526 | ||||||
chr22:43975575
|
G | C | 1 | a0001c0008t0001g0182 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.649-480G>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43975575 | ||||||
chr22:43975602
|
G | A | 1 | a0003c0003t0001g0067 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.649-453G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43975602 | ||||||
chr22:43975691
|
C | T | 4 | a0003c0003t0001g0001a0003c0003t0001g0054a0003c0003t0001g0058others(1): Show | 8 | HG01071.hp2 HG01123.hp2 HG01358.hp2 others(5): Show |
intron_variant | MODIFIER | c.649-364C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43975691 | ||||||
chr22:43975845
|
C | A | 1 | a0002c0001t0001g0220 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.649-210C>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43975845 | ||||||
chr22:43975845
|
C | G | 249 | a0001c0002t0001g0016a0001c0002t0001g0022a0001c0002t0001g0161others(246): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.649-210C>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 7/14 | chr22 | 43975845 | ||||||
chr22:43976189
|
G | A | 179 | a0001c0002t0001g0016a0001c0002t0001g0022a0001c0002t0001g0161others(176): Show | 192 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(189): Show |
splice_region_variant&intron_variant | LOW | c.777+6G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 8/14 | chr22 | 43976189 | ||||||
chr22:43976310
|
C | T | 178 | a0001c0002t0001g0016a0001c0002t0001g0022a0001c0002t0001g0161others(175): Show | 191 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.777+127C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 8/14 | chr22 | 43976310 | ||||||
chr22:43976336
|
G | T | 1 | a0001c0002t0002g0290 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.777+153G>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 8/14 | chr22 | 43976336 | ||||||
chr22:43976349
|
C | T | 1 | a0001c0004t0001g0130 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.777+166C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 8/14 | chr22 | 43976349 | ||||||
chr22:43976376
|
G | T | 1 | a0001c0007t0003g0320 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.777+193G>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 8/14 | chr22 | 43976376 | ||||||
chr22:43976406
|
C | G | 1 | a0001c0006t0001g0109 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.777+223C>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 8/14 | chr22 | 43976406 | ||||||
chr22:43976431
|
A | G | 3 | a0001c0009t0001g0052a0001c0009t0001g0053a0002c0011t0001g0230 | 3 | HG01433.hp1 HG02922.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.777+248A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 8/14 | chr22 | 43976431 | ||||||
chr22:43976451
|
C | T | 178 | a0001c0002t0001g0016a0001c0002t0001g0022a0001c0002t0001g0161others(175): Show | 191 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.777+268C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 8/14 | chr22 | 43976451 | ||||||
chr22:43976617
|
AAGGGCTC others(22): Show |
A | 1 | a0001c0004t0001g0120 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.778-130_778-102del others(29): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr22 | 43976617 | |||||
chr22:43976645
|
A | G | 7 | a0001c0006t0001g0101a0001c0006t0001g0103a0001c0006t0001g0104others(4): Show | 7 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.778-105A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 8/14 | chr22 | 43976645 | ||||||
chr22:43976941
|
T | C | 9 | a0001c0008t0001g0033a0001c0008t0001g0175a0001c0008t0001g0176others(6): Show | 9 | HG01109.hp2 HG02109.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.849+120T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 9/14 | chr22 | 43976941 | ||||||
chr22:43977072
|
A | G | 2 | a0001c0009t0001g0052a0001c0009t0001g0053 | 2 | HG01433.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.849+251A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 9/14 | chr22 | 43977072 | ||||||
chr22:43977177
|
C | T | 1 | a0001c0010t0001g0136 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.849+356C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 9/14 | chr22 | 43977177 | ||||||
chr22:43977213
|
A | G | 2 | a0001c0005t0001g0329a0001c0005t0001g0330 | 2 | HG02965.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.849+392A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 9/14 | chr22 | 43977213 | ||||||
chr22:43977251
|
G | A | 3 | a0001c0002t0001g0337a0001c0002t0001g0338a0001c0002t0001g0339 | 3 | HG02647.hp1 HG02965.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.849+430G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 9/14 | chr22 | 43977251 | ||||||
chr22:43977282
|
T | G | 1 | a0002c0001t0001g0233 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.849+461T>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 9/14 | chr22 | 43977282 | ||||||
chr22:43977456
|
G | A | 3 | a0001c0007t0005g0034a0001c0013t0001g0319a0001c0013t0001g0321 | 3 | HG02723.hp2 HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.850-416G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 9/14 | chr22 | 43977456 | ||||||
chr22:43977580
|
C | T | 1 | a0001c0005t0001g0155 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.850-292C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 9/14 | chr22 | 43977580 | ||||||
chr22:43977699
|
G | A | 71 | a0001c0004t0001g0002a0001c0004t0001g0005a0001c0004t0001g0013others(68): Show | 79 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.850-173G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 9/14 | chr22 | 43977699 | ||||||
chr22:43977722
|
A | G | 4 | a0001c0006t0001g0043a0001c0006t0001g0044a0001c0007t0001g0326others(1): Show | 4 | HG02451.hp1 HG03098.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.850-150A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 9/14 | chr22 | 43977722 | ||||||
chr22:43977779
|
C | T | 2 | a0003c0003t0001g0059a0003c0003t0001g0061 | 2 | HG01169.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.850-93C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 9/14 | chr22 | 43977779 | ||||||
chr22:43978065
|
G | T | 7 | a0001c0006t0001g0101a0001c0006t0001g0103a0001c0006t0001g0104others(4): Show | 7 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.936+107G>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43978065 | ||||||
chr22:43978067
|
G | A | 4 | a0001c0007t0001g0027a0001c0007t0001g0028a0001c0007t0001g0322others(1): Show | 6 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.936+109G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43978067 | ||||||
chr22:43978209
|
T | G | 1 | a0002c0001t0001g0277 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.936+251T>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43978209 | ||||||
chr22:43978315
|
G | T | 72 | a0001c0004t0001g0002a0001c0004t0001g0005a0001c0004t0001g0013others(69): Show | 80 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.936+357G>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43978315 | ||||||
chr22:43978343
|
G | A | 4 | a0001c0008t0001g0175a0001c0008t0001g0178a0001c0008t0001g0181others(1): Show | 4 | HG02559.hp1 HG03041.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.936+385G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43978343 | ||||||
chr22:43978378
|
T | C | 1 | a0001c0002t0002g0283 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.936+420T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43978378 | ||||||
chr22:43978387
|
A | G | 254 | a0001c0002t0001g0016a0001c0002t0001g0022a0001c0002t0001g0161others(251): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(272): Show |
intron_variant | MODIFIER | c.936+429A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43978387 | ||||||
chr22:43978432
|
C | CAAAA | 20 | a0001c0002t0001g0268a0001c0002t0002g0274a0001c0002t0004g0293others(17): Show | 20 | HG01496.hp1 HG02027.hp1 HG02080.hp1 others(17): Show |
intron_variant | MODIFIER | c.936+492_936+495dup others(4): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43978432 | |||||
chr22:43978432
|
C | CAAAAA | 189 | a0001c0002t0001g0022a0001c0002t0001g0166a0001c0002t0001g0189others(186): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.936+491_936+495dup others(5): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43978432 | |||||
chr22:43978432
|
C | CAAAAAA | 35 | a0001c0002t0001g0016a0001c0002t0001g0162a0001c0002t0001g0163others(32): Show | 36 | HG00438.hp2 HG00544.hp2 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.936+490_936+495dup others(6): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43978432 | |||||
chr22:43978432
|
CA | C | 7 | a0001c0007t0001g0027a0001c0007t0001g0028a0001c0007t0001g0322others(4): Show | 9 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.936+495delA | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43978432 | |||||
chr22:43978636
|
A | T | 7 | a0001c0008t0001g0033a0001c0008t0001g0175a0001c0008t0001g0178others(4): Show | 7 | HG02257.hp1 HG02486.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.936+678A>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43978636 | ||||||
chr22:43978636
|
AT | A | 9 | a0001c0004t0001g0120a0001c0004t0001g0140a0001c0004t0001g0147others(6): Show | 9 | HG01167.hp2 HG01943.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.936+693delT | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43978636 | |||||
chr22:43978637
|
T | A | 1 | a0001c0009t0001g0053 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.936+679T>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43978637 | ||||||
chr22:43978704
|
A | T | 254 | a0001c0002t0001g0016a0001c0002t0001g0022a0001c0002t0001g0161others(251): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(272): Show |
intron_variant | MODIFIER | c.936+746A>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43978704 | ||||||
chr22:43978751
|
G | A | 1 | a0002c0001t0001g0257 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.936+793G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43978751 | ||||||
chr22:43978883
|
G | T | 9 | a0001c0002t0001g0016a0001c0002t0001g0161a0001c0002t0001g0162others(6): Show | 10 | HG01891.hp1 HG01934.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.936+925G>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43978883 | ||||||
chr22:43979196
|
A | C | 1 | a0003c0016t0001g0100 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.936+1238A>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43979196 | ||||||
chr22:43979364
|
C | T | 254 | a0001c0002t0001g0016a0001c0002t0001g0022a0001c0002t0001g0161others(251): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(272): Show |
intron_variant | MODIFIER | c.936+1406C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43979364 | ||||||
chr22:43979367
|
A | C | 259 | a0001c0002t0001g0016a0001c0002t0001g0022a0001c0002t0001g0161others(256): Show | 282 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.936+1409A>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43979367 | ||||||
chr22:43979395
|
C | A | 182 | a0001c0002t0001g0016a0001c0002t0001g0022a0001c0002t0001g0161others(179): Show | 195 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.936+1437C>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43979395 | ||||||
chr22:43979558
|
C | T | 49 | a0001c0002t0002g0023a0001c0002t0002g0024a0001c0002t0002g0025others(46): Show | 53 | HG00099.hp2 HG00544.hp1 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.936+1600C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43979558 | ||||||
chr22:43979582
|
T | A | 1 | a0002c0012t0001g0153 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.936+1624T>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43979582 | ||||||
chr22:43979601
|
G | A | 2 | a0001c0004t0001g0132a0001c0004t0001g0143 | 2 | NA18953.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.936+1643G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43979601 | ||||||
chr22:43979627
|
T | C | 254 | a0001c0002t0001g0016a0001c0002t0001g0022a0001c0002t0001g0161others(251): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(272): Show |
intron_variant | MODIFIER | c.936+1669T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43979627 | ||||||
chr22:43979637
|
T | C | 1 | a0001c0004t0001g0120 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.936+1679T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43979637 | ||||||
chr22:43979862
|
C | T | 182 | a0001c0002t0001g0016a0001c0002t0001g0022a0001c0002t0001g0161others(179): Show | 195 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.937-1529C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43979862 | ||||||
chr22:43979981
|
A | C | 1 | a0002c0001t0001g0201 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.937-1410A>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43979981 | ||||||
chr22:43980022
|
C | T | 7 | a0001c0006t0001g0101a0001c0006t0001g0103a0001c0006t0001g0104others(4): Show | 7 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.937-1369C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43980022 | ||||||
chr22:43980065
|
C | T | 1 | a0001c0008t0001g0178 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.937-1326C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43980065 | ||||||
chr22:43980090
|
A | G | 182 | a0001c0002t0001g0016a0001c0002t0001g0022a0001c0002t0001g0161others(179): Show | 195 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.937-1301A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43980090 | ||||||
chr22:43980136
|
A | ACACATCC others(623): Show |
1 | a0002c0001t0001g0205 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.937-1253_937-1252i others(632): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(593): Show |
1 | a0003c0003t0001g0058 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.937-1228_937-1227i others(602): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(597): Show |
3 | a0003c0003t0001g0001a0003c0003t0001g0054a0003c0003t0001g0092 | 7 | HG01071.hp2 HG01123.hp2 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.937-1228_937-1227i others(606): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(613): Show |
1 | a0002c0001t0001g0050 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.937-1228_937-1227i others(622): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(917): Show |
2 | a0001c0007t0001g0027a0001c0007t0001g0028 | 4 | HG00280.hp2 HG00733.hp2 HG01109.hp1 others(1): Show |
intron_variant | MODIFIER | c.937-1228_937-1227i others(926): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(921): Show |
2 | a0001c0007t0001g0322a0001c0007t0001g0323 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.937-1228_937-1227i others(930): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(625): Show |
8 | a0002c0001t0001g0038a0002c0001t0001g0039a0002c0001t0001g0206others(5): Show | 8 | HG00408.hp2 HG01243.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.937-1228_937-1227i others(634): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(625): Show |
1 | a0002c0001t0001g0198 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.937-1228_937-1227i others(634): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(617): Show |
3 | a0002c0001t0001g0202a0002c0001t0001g0214a0002c0001t0001g0235 | 3 | HG00741.hp1 HG02056.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.937-1228_937-1227i others(626): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(621): Show |
2 | a0002c0001t0001g0231a0002c0001t0001g0252 | 2 | HG02027.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.937-1228_937-1227i others(630): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(621): Show |
49 | a0002c0001t0001g0006a0002c0001t0001g0017a0002c0001t0001g0018others(46): Show | 55 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.937-1228_937-1227i others(630): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(625): Show |
1 | a0002c0001t0001g0249 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.937-1228_937-1227i others(634): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(617): Show |
2 | a0002c0001t0001g0191a0002c0001t0001g0194 | 2 | HG02572.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.937-1228_937-1227i others(626): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(622): Show |
1 | a0002c0001t0001g0260 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.937-1228_937-1227i others(631): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(629): Show |
1 | a0002c0001t0001g0262 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.937-1228_937-1227i others(638): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(625): Show |
2 | a0002c0001t0001g0200a0002c0001t0001g0276 | 2 | NA18971.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.937-1228_937-1227i others(634): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(617): Show |
1 | a0002c0012t0001g0042 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.937-1228_937-1227i others(626): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(621): Show |
1 | a0002c0001t0001g0197 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.937-1228_937-1227i others(630): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(617): Show |
5 | a0002c0001t0001g0019a0002c0001t0001g0241a0002c0001t0001g0250others(2): Show | 6 | HG02015.hp1 HG03704.hp1 NA18946.hp1 others(3): Show |
intron_variant | MODIFIER | c.937-1228_937-1227i others(626): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(621): Show |
1 | a0001c0006t0001g0110 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.937-1228_937-1227i others(630): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(625): Show |
6 | a0002c0001t0001g0203a0002c0001t0001g0240a0002c0001t0001g0243others(3): Show | 6 | HG01255.hp1 HG02056.hp2 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.937-1228_937-1227i others(634): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(613): Show |
1 | a0002c0001t0001g0192 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.937-1228_937-1227i others(622): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(613): Show |
1 | a0001c0002t0001g0266 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.937-1228_937-1227i others(622): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(617): Show |
6 | a0001c0002t0001g0022a0001c0002t0001g0265a0001c0002t0001g0267others(3): Show | 7 | HG00423.hp1 HG04204.hp1 NA18963.hp2 others(4): Show |
intron_variant | MODIFIER | c.937-1228_937-1227i others(626): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(617): Show |
1 | a0002c0001t0001g0193 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.937-1228_937-1227i others(626): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(617): Show |
1 | a0002c0001t0001g0233 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.937-1228_937-1227i others(626): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(609): Show |
1 | a0003c0003t0001g0009 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.937-1228_937-1227i others(618): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(605): Show |
4 | a0001c0020t0001g0327a0003c0003t0001g0056a0003c0003t0001g0063others(1): Show | 4 | HG02145.hp2 HG02647.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.937-1228_937-1227i others(614): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(601): Show |
1 | a0003c0003t0001g0076 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.937-1228_937-1227i others(610): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(617): Show |
3 | a0003c0003t0001g0057a0003c0003t0001g0084a0003c0003t0001g0089 | 3 | HG00642.hp1 HG01081.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.937-1228_937-1227i others(626): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(613): Show |
28 | a0003c0003t0001g0003a0003c0003t0001g0004a0003c0003t0001g0008others(25): Show | 36 | HG00140.hp1 HG00408.hp1 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.937-1228_937-1227i others(622): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(617): Show |
1 | a0003c0003t0001g0077 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.937-1228_937-1227i others(626): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(605): Show |
1 | a0004c0015t0001g0078 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.937-1228_937-1227i others(614): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(609): Show |
12 | a0003c0003t0001g0007a0003c0003t0001g0046a0003c0003t0001g0049others(9): Show | 13 | HG00558.hp2 HG01169.hp1 HG02015.hp2 others(10): Show |
intron_variant | MODIFIER | c.937-1228_937-1227i others(618): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(605): Show |
1 | a0003c0003t0001g0091 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.937-1228_937-1227i others(614): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(609): Show |
1 | a0003c0003t0001g0067 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.937-1228_937-1227i others(618): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(613): Show |
1 | a0003c0003t0001g0061 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.937-1228_937-1227i others(622): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(613): Show |
1 | a0003c0003t0001g0111 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.937-1228_937-1227i others(622): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(609): Show |
1 | a0001c0009t0001g0052 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.937-1228_937-1227i others(618): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(941): Show |
1 | a0001c0007t0003g0320 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.937-1228_937-1227i others(950): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(621): Show |
1 | a0001c0002t0001g0338 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.937-1228_937-1227i others(630): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(621): Show |
1 | a0001c0002t0001g0337 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.937-1228_937-1227i others(630): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(629): Show |
1 | a0001c0002t0001g0339 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.937-1228_937-1227i others(638): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(625): Show |
3 | a0001c0002t0002g0023a0001c0002t0002g0040a0001c0002t0002g0272 | 4 | HG02258.hp2 HG02717.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.937-1228_937-1227i others(634): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(625): Show |
1 | a0002c0001t0001g0196 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.937-1228_937-1227i others(634): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(621): Show |
2 | a0001c0006t0001g0104a0001c0006t0001g0107 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.937-1228_937-1227i others(630): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(625): Show |
4 | a0001c0006t0001g0101a0001c0006t0001g0103a0001c0006t0001g0108others(1): Show | 4 | HG02055.hp1 HG02818.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.937-1228_937-1227i others(634): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(625): Show |
1 | a0001c0002t0001g0188 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.937-1228_937-1227i others(634): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(629): Show |
1 | a0001c0008t0001g0175 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.937-1228_937-1227i others(638): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(625): Show |
1 | a0001c0008t0001g0180 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.937-1228_937-1227i others(634): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(585): Show |
1 | a0001c0002t0002g0283 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.937-1228_937-1227i others(594): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(581): Show |
1 | a0001c0002t0002g0294 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.937-1228_937-1227i others(590): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(581): Show |
2 | a0001c0002t0002g0183a0001c0002t0002g0280 | 2 | HG02258.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.937-1228_937-1227i others(590): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(585): Show |
1 | a0001c0002t0002g0288 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.937-1228_937-1227i others(594): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(597): Show |
1 | a0001c0002t0002g0314 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.937-1228_937-1227i others(606): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(581): Show |
1 | a0001c0002t0002g0285 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.937-1228_937-1227i others(590): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(593): Show |
4 | a0001c0002t0002g0295a0001c0002t0002g0304a0001c0002t0002g0305others(1): Show | 4 | HG00099.hp2 HG01243.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.937-1228_937-1227i others(602): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(581): Show |
10 | a0001c0002t0002g0185a0001c0002t0002g0286a0001c0002t0002g0290others(7): Show | 10 | HG02486.hp1 HG02572.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.937-1228_937-1227i others(590): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(597): Show |
18 | a0001c0002t0002g0025a0001c0002t0002g0026a0001c0002t0002g0184others(15): Show | 20 | HG00544.hp1 HG00558.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.937-1228_937-1227i others(606): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(601): Show |
1 | a0001c0002t0002g0297 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.937-1228_937-1227i others(610): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(593): Show |
5 | a0001c0002t0002g0024a0001c0002t0002g0287a0001c0002t0002g0302others(2): Show | 6 | HG04199.hp2 NA18972.hp1 NA18981.hp2 others(3): Show |
intron_variant | MODIFIER | c.937-1228_937-1227i others(602): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(629): Show |
2 | a0001c0002t0002g0270a0001c0002t0002g0271 | 2 | HG03486.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.937-1228_937-1227i others(638): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(593): Show |
1 | a0001c0004t0001g0045 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.937-1228_937-1227i others(602): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(605): Show |
2 | a0002c0011t0001g0035a0002c0011t0001g0248 | 2 | HG00639.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.937-1228_937-1227i others(614): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(605): Show |
1 | a0001c0004t0001g0173 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.937-1228_937-1227i others(614): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(593): Show |
1 | a0001c0004t0001g0147 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.937-1228_937-1227i others(602): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(597): Show |
1 | a0001c0010t0001g0124 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.937-1228_937-1227i others(606): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(601): Show |
2 | a0001c0010t0001g0136a0001c0010t0001g0145 | 2 | HG02615.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.937-1228_937-1227i others(610): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(601): Show |
57 | a0001c0004t0001g0002a0001c0004t0001g0005a0001c0004t0001g0013others(54): Show | 65 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.937-1228_937-1227i others(610): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(605): Show |
2 | a0001c0004t0001g0150a0002c0012t0001g0149 | 2 | HG01433.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.937-1228_937-1227i others(614): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(597): Show |
2 | a0001c0004t0001g0146a0001c0004t0002g0037 | 2 | HG02257.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.937-1228_937-1227i others(606): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(597): Show |
1 | a0001c0009t0001g0053 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.937-1228_937-1227i others(606): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(617): Show |
5 | a0001c0005t0001g0029a0001c0005t0001g0329a0001c0005t0001g0330others(2): Show | 6 | HG02055.hp2 HG02886.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.937-1228_937-1227i others(626): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(613): Show |
4 | a0001c0005t0001g0328a0001c0005t0001g0331a0001c0005t0001g0332others(1): Show | 4 | HG02280.hp1 HG02615.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.937-1228_937-1227i others(622): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(597): Show |
1 | a0002c0011t0001g0230 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.937-1228_937-1227i others(606): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(901): Show |
1 | a0001c0004t0001g0159 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.937-1228_937-1227i others(910): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(613): Show |
1 | a0001c0005t0001g0155 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.937-1228_937-1227i others(622): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(606): Show |
1 | a0001c0004t0001g0120 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.937-1228_937-1227i others(615): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(605): Show |
2 | a0001c0002t0001g0016a0001c0002t0001g0163 | 3 | HG01891.hp1 HG02280.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.937-1228_937-1227i others(614): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(609): Show |
2 | a0001c0002t0001g0165a0001c0002t0001g0166 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.937-1228_937-1227i others(618): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(597): Show |
1 | a0001c0008t0001g0176 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.937-1228_937-1227i others(606): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(605): Show |
3 | a0001c0002t0001g0161a0001c0002t0001g0168a0001c0008t0001g0177 | 3 | HG01109.hp2 HG02630.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.937-1228_937-1227i others(614): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(609): Show |
2 | a0001c0002t0001g0162a0001c0002t0001g0164 | 2 | HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.937-1228_937-1227i others(618): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(613): Show |
1 | a0001c0013t0001g0321 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.937-1228_937-1227i others(622): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(621): Show |
1 | a0001c0007t0005g0034 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.937-1228_937-1227i others(630): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(629): Show |
2 | a0001c0008t0001g0178a0001c0008t0001g0182 | 2 | HG02559.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.937-1228_937-1227i others(638): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(633): Show |
3 | a0001c0008t0001g0033a0001c0008t0001g0179a0001c0008t0001g0181 | 3 | HG02257.hp1 HG02717.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.937-1228_937-1227i others(642): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(625): Show |
1 | a0001c0013t0001g0319 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.937-1228_937-1227i others(634): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(625): Show |
1 | a0001c0007t0001g0326 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.937-1228_937-1227i others(634): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(629): Show |
1 | a0001c0006t0001g0043 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.937-1228_937-1227i others(638): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(625): Show |
1 | a0001c0006t0001g0044 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.937-1228_937-1227i others(634): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(605): Show |
3 | a0001c0004t0001g0135a0001c0004t0001g0156a0001c0004t0001g0158 | 3 | HG01346.hp2 NA18979.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.937-1228_937-1227i others(614): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980136
|
A | ACATCCAT others(609): Show |
1 | a0001c0002t0001g0167 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.937-1228_937-1227i others(618): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980136 | |||||
chr22:43980139
|
T | TCCATCCA others(605): Show |
3 | a0003c0003t0001g0011a0003c0003t0001g0048a0003c0003t0001g0087 | 4 | HG00642.hp2 HG01346.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.937-1228_937-1227i others(614): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980139 | |||||
chr22:43980139
|
T | TCCATCCA others(613): Show |
1 | a0003c0003t0001g0088 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.937-1228_937-1227i others(622): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980139 | |||||
chr22:43980139
|
T | TCCATCCA others(609): Show |
1 | a0001c0002t0001g0189 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.937-1228_937-1227i others(618): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980139 | |||||
chr22:43980161
|
C | CATCCATC others(609): Show |
1 | a0003c0003t0001g0051 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.937-1228_937-1227i others(618): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr22 | 43980161 | |||||
chr22:43980455
|
C | T | 187 | a0001c0002t0001g0016a0001c0002t0001g0022a0001c0002t0001g0161others(184): Show | 202 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.937-936C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43980455 | ||||||
chr22:43980479
|
G | A | 1 | a0001c0004t0001g0120 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.937-912G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43980479 | ||||||
chr22:43980512
|
C | T | 1 | a0003c0003t0001g0077 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.937-879C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43980512 | ||||||
chr22:43980582
|
C | A | 11 | a0001c0002t0001g0016a0001c0002t0001g0161a0001c0002t0001g0162others(8): Show | 12 | HG01109.hp2 HG01891.hp1 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.937-809C>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43980582 | ||||||
chr22:43980595
|
G | A | 1 | a0001c0005t0001g0155 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.937-796G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43980595 | ||||||
chr22:43980610
|
T | A | 11 | a0001c0002t0001g0022a0001c0002t0001g0189a0001c0002t0001g0265others(8): Show | 12 | HG00423.hp1 HG02451.hp1 HG03098.hp1 others(9): Show |
intron_variant | MODIFIER | c.937-781T>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43980610 | ||||||
chr22:43980634
|
G | C | 1 | a0001c0007t0003g0320 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.937-757G>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43980634 | ||||||
chr22:43980903
|
G | T | 1 | a0001c0004t0001g0120 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.937-488G>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43980903 | ||||||
chr22:43980944
|
T | C | 1 | a0001c0004t0001g0045 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.937-447T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43980944 | ||||||
chr22:43981015
|
A | T | 1 | a0001c0004t0001g0120 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.937-376A>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43981015 | ||||||
chr22:43981133
|
G | A | 10 | a0001c0005t0001g0029a0001c0005t0001g0328a0001c0005t0001g0329others(7): Show | 11 | HG02055.hp2 HG02280.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.937-258G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43981133 | ||||||
chr22:43981144
|
G | A | 1 | a0001c0004t0001g0140 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.937-247G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43981144 | ||||||
chr22:43981155
|
G | A | 1 | a0001c0008t0001g0177 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.937-236G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43981155 | ||||||
chr22:43981297
|
C | T | 1 | a0001c0002t0001g0269 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.937-94C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43981297 | ||||||
chr22:43981341
|
G | T | 4 | a0001c0007t0001g0027a0001c0007t0001g0028a0001c0007t0001g0322others(1): Show | 6 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.937-50G>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 10/14 | chr22 | 43981341 | ||||||
chr22:43981562
|
A | G | 188 | a0001c0002t0001g0016a0001c0002t0001g0022a0001c0002t0001g0161others(185): Show | 203 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.1007+101A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 11/14 | chr22 | 43981562 | ||||||
chr22:43981563
|
T | C | 2 | a0003c0003t0001g0076a0003c0003t0001g0096 | 2 | HG03831.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1007+102T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 11/14 | chr22 | 43981563 | ||||||
chr22:43981677
|
A | C | 63 | a0001c0002t0001g0022a0001c0002t0001g0189a0001c0002t0001g0265others(60): Show | 68 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.1007+216A>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 11/14 | chr22 | 43981677 | ||||||
chr22:43981680
|
G | A | 1 | a0001c0004t0001g0137 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1007+219G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 11/14 | chr22 | 43981680 | ||||||
chr22:43981842
|
A | C | 3 | a0001c0009t0001g0052a0001c0009t0001g0053a0002c0011t0001g0230 | 3 | HG01433.hp1 HG02922.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1007+381A>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 11/14 | chr22 | 43981842 | ||||||
chr22:43982072
|
G | A | 1 | a0002c0001t0001g0203 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1007+611G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 11/14 | chr22 | 43982072 | ||||||
chr22:43982103
|
A | C | 4 | a0003c0003t0001g0001a0003c0003t0001g0054a0003c0003t0001g0058others(1): Show | 8 | HG01071.hp2 HG01123.hp2 HG01358.hp2 others(5): Show |
intron_variant | MODIFIER | c.1007+642A>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 11/14 | chr22 | 43982103 | ||||||
chr22:43982119
|
C | T | 115 | a0001c0002t0001g0016a0001c0002t0001g0161a0001c0002t0001g0162others(112): Show | 123 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.1007+658C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 11/14 | chr22 | 43982119 | ||||||
chr22:43982342
|
C | T | 1 | a0002c0001t0001g0233 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1007+881C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 11/14 | chr22 | 43982342 | ||||||
chr22:43982350
|
G | A | 2 | a0001c0006t0001g0104a0001c0006t0001g0107 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1007+889G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 11/14 | chr22 | 43982350 | ||||||
chr22:43982426
|
T | G | 1 | a0003c0003t0001g0077 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1007+965T>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 11/14 | chr22 | 43982426 | ||||||
chr22:43982447
|
G | A | 4 | a0001c0004t0001g0036a0001c0004t0001g0116a0001c0004t0001g0142others(1): Show | 4 | HG00735.hp1 NA18971.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.1007+986G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 11/14 | chr22 | 43982447 | ||||||
chr22:43982488
|
C | T | 2 | a0001c0004t0001g0013a0001c0004t0001g0119 | 3 | NA18952.hp1 NA18963.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1007+1027C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 11/14 | chr22 | 43982488 | ||||||
chr22:43982522
|
C | T | 2 | a0003c0003t0001g0084a0003c0003t0001g0089 | 2 | HG00642.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.1007+1061C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 11/14 | chr22 | 43982522 | ||||||
chr22:43982626
|
T | C | 2 | a0001c0002t0002g0270a0001c0002t0002g0271 | 2 | HG03486.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1007+1165T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 11/14 | chr22 | 43982626 | ||||||
chr22:43982704
|
C | T | 1 | a0002c0001t0001g0219 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1008-1229C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 11/14 | chr22 | 43982704 | ||||||
chr22:43982790
|
C | T | 3 | a0002c0001t0001g0196a0002c0001t0001g0204a0002c0001t0001g0209 | 3 | HG01099.hp2 HG01261.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.1008-1143C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 11/14 | chr22 | 43982790 | ||||||
chr22:43982792
|
C | A | 112 | a0001c0002t0001g0016a0001c0002t0001g0161a0001c0002t0001g0162others(109): Show | 120 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.1008-1141C>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 11/14 | chr22 | 43982792 | ||||||
chr22:43982824
|
C | A | 1 | a0001c0007t0003g0320 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1008-1109C>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 11/14 | chr22 | 43982824 | ||||||
chr22:43982929
|
C | T | 115 | a0001c0002t0001g0016a0001c0002t0001g0161a0001c0002t0001g0162others(112): Show | 123 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.1008-1004C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 11/14 | chr22 | 43982929 | ||||||
chr22:43982958
|
C | T | 1 | a0002c0001t0001g0245 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1008-975C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 11/14 | chr22 | 43982958 | ||||||
chr22:43983171
|
G | A | 7 | a0001c0006t0001g0101a0001c0006t0001g0103a0001c0006t0001g0104others(4): Show | 7 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.1008-762G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 11/14 | chr22 | 43983171 | ||||||
chr22:43983251
|
A | C | 1 | a0001c0004t0001g0128 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1008-682A>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 11/14 | chr22 | 43983251 | ||||||
chr22:43983627
|
C | G | 2 | a0001c0013t0001g0319a0001c0013t0001g0321 | 2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1008-306C>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 11/14 | chr22 | 43983627 | ||||||
chr22:43983685
|
G | C | 129 | a0001c0002t0001g0016a0001c0002t0001g0161a0001c0002t0001g0162others(126): Show | 139 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.1008-248G>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 11/14 | chr22 | 43983685 | ||||||
chr22:43983772
|
T | C | 2 | a0002c0001t0001g0223a0002c0001t0001g0234 | 2 | HG01257.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1008-161T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 11/14 | chr22 | 43983772 | ||||||
chr22:43983851
|
CAT | C | 9 | a0001c0006t0001g0043a0001c0006t0001g0044a0001c0006t0001g0101others(6): Show | 9 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1008-81_1008-80del others(2): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 11/14 | chr22 | 43983851 | ||||||
chr22:43983860
|
C | A | 115 | a0001c0002t0001g0016a0001c0002t0001g0161a0001c0002t0001g0162others(112): Show | 123 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.1008-73C>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 11/14 | chr22 | 43983860 | ||||||
chr22:43984043
|
G | A | 1 | a0002c0011t0001g0248 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1075+43G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43984043 | ||||||
chr22:43984129
|
A | G | 114 | a0001c0002t0001g0016a0001c0002t0001g0161a0001c0002t0001g0162others(111): Show | 122 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.1075+129A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43984129 | ||||||
chr22:43984153
|
T | C | 60 | a0001c0002t0001g0022a0001c0002t0001g0189a0001c0002t0001g0265others(57): Show | 65 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.1075+153T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43984153 | ||||||
chr22:43984290
|
G | GCTTC | 116 | a0001c0002t0001g0016a0001c0002t0001g0161a0001c0002t0001g0162others(113): Show | 124 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.1075+293_1075+296d others(6): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 43984290 | |||||
chr22:43984301
|
T | C | 1 | a0002c0001t0001g0192 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1075+301T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43984301 | ||||||
chr22:43984312
|
A | G | 1 | a0001c0008t0001g0175 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1075+312A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43984312 | ||||||
chr22:43984373
|
C | T | 2 | a0001c0002t0001g0189a0001c0007t0001g0326 | 2 | HG03195.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1075+373C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43984373 | ||||||
chr22:43984721
|
C | T | 2 | a0001c0002t0002g0282a0001c0002t0002g0297 | 2 | HG01261.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.1075+721C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43984721 | ||||||
chr22:43984754
|
G | A | 1 | a0001c0009t0001g0052 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1075+754G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43984754 | ||||||
chr22:43984769
|
C | T | 11 | a0001c0002t0001g0016a0001c0002t0001g0161a0001c0002t0001g0162others(8): Show | 12 | HG01109.hp2 HG01891.hp1 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.1075+769C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43984769 | ||||||
chr22:43984776
|
A | G | 18 | a0001c0002t0001g0016a0001c0002t0001g0161a0001c0002t0001g0162others(15): Show | 19 | HG01109.hp2 HG01891.hp1 HG01934.hp2 others(16): Show |
intron_variant | MODIFIER | c.1075+776A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43984776 | ||||||
chr22:43984831
|
TATGTTGG others(1403): Show |
T | 7 | a0001c0006t0001g0101a0001c0006t0001g0103a0001c0006t0001g0104others(4): Show | 7 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.1075+843_1075+2252 others(3): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 43984831 | |||||
chr22:43984887
|
T | C | 115 | a0001c0002t0001g0016a0001c0002t0001g0161a0001c0002t0001g0162others(112): Show | 123 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.1075+887T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43984887 | ||||||
chr22:43985008
|
C | T | 3 | a0001c0006t0001g0043a0001c0006t0001g0044a0002c0012t0001g0042 | 3 | HG02451.hp1 HG03098.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1075+1008C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43985008 | ||||||
chr22:43985131
|
AC | A | 4 | a0001c0002t0001g0188a0001c0002t0001g0337a0001c0002t0001g0338others(1): Show | 4 | HG02647.hp1 HG02965.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1075+1136delC | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 43985131 | |||||
chr22:43985297
|
T | A | 1 | a0003c0003t0001g0095 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1075+1297T>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43985297 | ||||||
chr22:43985343
|
G | C | 327 | a0001c0002t0001g0016a0001c0002t0001g0022a0001c0002t0001g0161others(324): Show | 365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.1075+1343G>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43985343 | ||||||
chr22:43985415
|
C | A | 1 | a0003c0003t0001g0095 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1075+1415C>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43985415 | ||||||
chr22:43985460
|
T | C | 116 | a0001c0002t0001g0016a0001c0002t0001g0161a0001c0002t0001g0162others(113): Show | 124 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.1075+1460T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43985460 | ||||||
chr22:43985602
|
C | T | 89 | a0001c0002t0002g0278a0002c0001t0001g0006a0002c0001t0001g0017others(86): Show | 96 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.1075+1602C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43985602 | ||||||
chr22:43985665
|
C | T | 253 | a0001c0002t0001g0016a0001c0002t0001g0022a0001c0002t0001g0161others(250): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(273): Show |
intron_variant | MODIFIER | c.1075+1665C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43985665 | ||||||
chr22:43985983
|
C | T | 3 | a0001c0008t0001g0033a0001c0008t0001g0179a0001c0008t0001g0180 | 3 | HG02257.hp1 HG02486.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1075+1983C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43985983 | ||||||
chr22:43986012
|
T | TTTTA | 11 | a0001c0002t0001g0016a0001c0002t0001g0161a0001c0002t0001g0162others(8): Show | 12 | HG01109.hp2 HG01891.hp1 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.1075+2028_1075+203 others(8): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 43986012 | |||||
chr22:43986021
|
T | G | 1 | a0003c0003t0001g0079 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1075+2021T>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43986021 | ||||||
chr22:43986043
|
C | CT | 14 | a0001c0004t0001g0005a0001c0004t0001g0113a0001c0004t0001g0118others(11): Show | 16 | HG00609.hp1 HG01175.hp1 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.1075+2060dupT | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 43986043 | |||||
chr22:43986045
|
T | TTC | 12 | a0001c0002t0001g0016a0001c0002t0001g0161a0001c0002t0001g0162others(9): Show | 13 | HG01109.hp2 HG01891.hp1 HG01934.hp2 others(10): Show |
intron_variant | MODIFIER | c.1075+2046_1075+204 others(6): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 43986045 | |||||
chr22:43986046
|
T | TC | 163 | a0001c0002t0001g0022a0001c0002t0001g0166a0001c0002t0001g0188others(160): Show | 175 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.1075+2046_1075+204 others(5): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43986046 | ||||||
chr22:43986064
|
ATGGAGTC others(6): Show |
A | 178 | a0001c0002t0001g0016a0001c0002t0001g0022a0001c0002t0001g0161others(175): Show | 191 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.1075+2067_1075+207 others(17): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 43986064 | |||||
chr22:43986124
|
C | A | 174 | a0001c0002t0001g0016a0001c0002t0001g0022a0001c0002t0001g0161others(171): Show | 187 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.1075+2124C>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43986124 | ||||||
chr22:43986191
|
G | A | 1 | a0001c0002t0001g0188 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1075+2191G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43986191 | ||||||
chr22:43986192
|
C | T | 39 | a0001c0002t0001g0016a0001c0002t0001g0161a0001c0002t0001g0162others(36): Show | 40 | HG01109.hp2 HG01243.hp1 HG01891.hp1 others(37): Show |
intron_variant | MODIFIER | c.1075+2192C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43986192 | ||||||
chr22:43986254
|
C | A | 1 | a0002c0001t0001g0227 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1075+2254C>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43986254 | ||||||
chr22:43986276
|
G | A | 3 | a0001c0009t0001g0053a0001c0013t0001g0319a0001c0013t0001g0321 | 3 | HG01433.hp1 HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1075+2276G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43986276 | ||||||
chr22:43986287
|
G | A | 1 | a0001c0010t0001g0145 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1075+2287G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43986287 | ||||||
chr22:43986367
|
A | C | 53 | a0001c0002t0002g0023a0001c0002t0002g0024a0001c0002t0002g0025others(50): Show | 57 | HG00099.hp2 HG00544.hp1 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.1075+2367A>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43986367 | ||||||
chr22:43986455
|
A | G | 1 | a0001c0007t0003g0320 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1075+2455A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43986455 | ||||||
chr22:43986457
|
A | G | 3 | a0001c0004t0001g0036a0001c0004t0001g0116a0001c0004t0002g0037 | 3 | NA18971.hp1 NA19062.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1075+2457A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43986457 | ||||||
chr22:43986653
|
C | T | 174 | a0001c0002t0001g0016a0001c0002t0001g0022a0001c0002t0001g0161others(171): Show | 188 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.1076-2458C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43986653 | ||||||
chr22:43986804
|
T | C | 187 | a0001c0002t0001g0016a0001c0002t0001g0022a0001c0002t0001g0161others(184): Show | 203 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.1076-2307T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43986804 | ||||||
chr22:43986825
|
T | G | 18 | a0001c0002t0001g0016a0001c0002t0001g0161a0001c0002t0001g0162others(15): Show | 19 | HG01109.hp2 HG01891.hp1 HG01934.hp2 others(16): Show |
intron_variant | MODIFIER | c.1076-2286T>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43986825 | ||||||
chr22:43986844
|
C | T | 1 | a0001c0002t0002g0026 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1076-2267C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43986844 | ||||||
chr22:43986899
|
T | C | 1 | a0002c0001t0001g0262 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1076-2212T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43986899 | ||||||
chr22:43986973
|
G | A | 62 | a0001c0002t0001g0022a0001c0002t0001g0189a0001c0002t0001g0265others(59): Show | 67 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.1076-2138G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43986973 | ||||||
chr22:43987190
|
T | C | 8 | a0001c0007t0001g0027a0001c0007t0001g0028a0001c0007t0001g0322others(5): Show | 10 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.1076-1921T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43987190 | ||||||
chr22:43987242
|
A | G | 1 | a0001c0008t0001g0175 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1076-1869A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43987242 | ||||||
chr22:43987508
|
G | A | 1 | a0001c0004t0001g0156 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1076-1603G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43987508 | ||||||
chr22:43987520
|
C | T | 187 | a0001c0002t0001g0016a0001c0002t0001g0022a0001c0002t0001g0161others(184): Show | 203 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.1076-1591C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43987520 | ||||||
chr22:43987523
|
G | C | 4 | a0003c0003t0001g0001a0003c0003t0001g0054a0003c0003t0001g0058others(1): Show | 8 | HG01071.hp2 HG01123.hp2 HG01358.hp2 others(5): Show |
intron_variant | MODIFIER | c.1076-1588G>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43987523 | ||||||
chr22:43987552
|
G | C | 187 | a0001c0002t0001g0016a0001c0002t0001g0022a0001c0002t0001g0161others(184): Show | 203 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.1076-1559G>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43987552 | ||||||
chr22:43987560
|
G | A | 1 | a0001c0004t0001g0148 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1076-1551G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43987560 | ||||||
chr22:43987622
|
T | C | 8 | a0001c0007t0001g0027a0001c0007t0001g0028a0001c0007t0001g0322others(5): Show | 10 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.1076-1489T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43987622 | ||||||
chr22:43987737
|
C | G | 195 | a0001c0002t0001g0016a0001c0002t0001g0022a0001c0002t0001g0161others(192): Show | 211 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.1076-1374C>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43987737 | ||||||
chr22:43987793
|
A | T | 2 | a0001c0004t0001g0013a0001c0004t0001g0119 | 3 | NA18952.hp1 NA18963.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1076-1318A>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43987793 | ||||||
chr22:43987880
|
A | AG | 4 | a0001c0007t0003g0320a0001c0010t0001g0124a0001c0010t0001g0136others(1): Show | 4 | HG02615.hp1 HG02809.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1076-1230dupG | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 43987880 | |||||
chr22:43987898
|
G | GTA | 18 | a0001c0004t0001g0134a0001c0005t0001g0029a0001c0005t0001g0328others(15): Show | 22 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.1076-1198_1076-119 others(6): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 43987898 | |||||
chr22:43987898
|
G | GTATA | 143 | a0001c0002t0001g0022a0001c0002t0001g0265a0001c0002t0001g0266others(140): Show | 154 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.1076-1200_1076-119 others(8): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 43987898 | |||||
chr22:43987898
|
G | GTATATA | 16 | a0001c0002t0001g0016a0001c0002t0001g0163a0001c0002t0001g0165others(13): Show | 17 | HG00639.hp1 HG01099.hp2 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.1076-1202_1076-119 others(10): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 43987898 | |||||
chr22:43987898
|
G | GTATATAT others(1): Show |
3 | a0001c0002t0001g0188a0001c0008t0001g0179a0001c0008t0001g0180 | 3 | HG02257.hp1 HG02486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1076-1204_1076-119 others(12): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 43987898 | |||||
chr22:43987898
|
G | GTATATAT others(3): Show |
2 | a0001c0002t0004g0293a0001c0008t0001g0033 | 2 | HG02717.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1076-1206_1076-119 others(14): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 43987898 | |||||
chr22:43987898
|
G | GTATATAT others(5): Show |
3 | a0001c0002t0001g0161a0001c0002t0001g0162a0001c0002t0001g0164 | 3 | HG02622.hp1 HG02809.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1076-1208_1076-119 others(16): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 43987898 | |||||
chr22:43987898
|
G | GTATATAT others(7): Show |
2 | a0001c0008t0001g0176a0001c0008t0001g0177 | 2 | HG01109.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.1076-1210_1076-119 others(18): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 43987898 | |||||
chr22:43987898
|
G | GTGTA | 3 | a0002c0001t0001g0018a0002c0001t0001g0206a0002c0001t0001g0232 | 4 | NA18947.hp1 NA18970.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.1076-1212_1076-121 others(8): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 43987898 | |||||
chr22:43987913
|
T | C | 9 | a0003c0003t0001g0049a0003c0003t0001g0062a0003c0003t0001g0073others(6): Show | 9 | HG00621.hp1 HG02145.hp1 NA18949.hp2 others(6): Show |
intron_variant | MODIFIER | c.1076-1198T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43987913 | ||||||
chr22:43987913
|
T | TATACAC | 4 | a0001c0008t0001g0175a0001c0008t0001g0178a0001c0008t0001g0181others(1): Show | 4 | HG02559.hp1 HG03041.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1076-1197_1076-119 others(10): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 43987913 | |||||
chr22:43987913
|
T | TATATATA others(7): Show |
1 | a0001c0007t0005g0034 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1076-1197_1076-119 others(18): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 43987913 | |||||
chr22:43987921
|
C | G | 1 | a0001c0004t0001g0318 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1076-1190C>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43987921 | ||||||
chr22:43988017
|
T | A | 1 | a0001c0004t0001g0114 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1076-1094T>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43988017 | ||||||
chr22:43988399
|
C | G | 51 | a0001c0002t0002g0023a0001c0002t0002g0024a0001c0002t0002g0025others(48): Show | 55 | HG00099.hp2 HG00544.hp1 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.1076-712C>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43988399 | ||||||
chr22:43988488
|
G | GT | 5 | a0003c0003t0001g0004a0003c0003t0001g0008a0003c0003t0001g0009others(2): Show | 9 | HG01099.hp1 HG01167.hp2 HG01515.hp2 others(6): Show |
intron_variant | MODIFIER | c.1076-618dupT | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 43988488 | |||||
chr22:43988545
|
G | A | 2 | a0002c0001t0001g0038a0002c0001t0001g0039 | 2 | HG01243.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1076-566G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43988545 | ||||||
chr22:43988741
|
T | G | 7 | a0001c0008t0001g0033a0001c0008t0001g0175a0001c0008t0001g0178others(4): Show | 7 | HG02257.hp1 HG02486.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1076-370T>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43988741 | ||||||
chr22:43988920
|
C | T | 2 | a0001c0002t0004g0293a0001c0007t0005g0034 | 2 | HG03195.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1076-191C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43988920 | ||||||
chr22:43989001
|
G | C | 61 | a0001c0002t0001g0022a0001c0002t0001g0189a0001c0002t0001g0265others(58): Show | 66 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.1076-110G>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 12/14 | chr22 | 43989001 | ||||||
chr22:43989268
|
C | T | 4 | a0003c0003t0001g0001a0003c0003t0001g0054a0003c0003t0001g0058others(1): Show | 8 | HG01071.hp2 HG01123.hp2 HG01358.hp2 others(5): Show |
intron_variant | MODIFIER | c.1222+11C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 13/14 | chr22 | 43989268 | ||||||
chr22:43989276
|
A | T | 1 | a0003c0003t0001g0058 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1222+19A>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 13/14 | chr22 | 43989276 | ||||||
chr22:43989339
|
C | CT | 70 | a0001c0002t0001g0022a0001c0002t0001g0189a0001c0002t0001g0265others(67): Show | 75 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.1222+98dupT | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 43989339 | |||||
chr22:43989339
|
C | CTT | 115 | a0001c0002t0001g0016a0001c0002t0001g0161a0001c0002t0001g0162others(112): Show | 126 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.1222+97_1222+98dup others(2): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 43989339 | |||||
chr22:43989661
|
A | G | 1 | a0003c0003t0001g0064 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1222+404A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 13/14 | chr22 | 43989661 | ||||||
chr22:43989703
|
T | C | 8 | a0001c0007t0001g0027a0001c0007t0001g0028a0001c0007t0001g0322others(5): Show | 10 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.1222+446T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 13/14 | chr22 | 43989703 | ||||||
chr22:43989714
|
A | G | 98 | a0001c0002t0001g0188a0001c0002t0001g0337a0001c0002t0001g0338others(95): Show | 106 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.1222+457A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 13/14 | chr22 | 43989714 | ||||||
chr22:43989788
|
C | T | 1 | a0002c0001t0001g0205 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1223-477C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 13/14 | chr22 | 43989788 | ||||||
chr22:43989799
|
CTGTT | C | 29 | a0001c0002t0002g0024a0001c0002t0002g0025a0001c0002t0002g0026others(26): Show | 32 | HG00099.hp2 HG00544.hp1 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.1223-462_1223-459d others(6): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 43989799 | |||||
chr22:43990409
|
A | ACGTGTTG others(9): Show |
1 | a0001c0002t0001g0188 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1364+4_1364+19dupC others(15): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr22 | 43990409 | |||||
chr22:43990549
|
T | C | 2 | a0001c0002t0004g0293a0001c0007t0005g0034 | 2 | HG03195.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1364+143T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43990549 | ||||||
chr22:43990758
|
G | A | 20 | a0001c0002t0001g0016a0001c0002t0001g0161a0001c0002t0001g0162others(17): Show | 21 | HG01109.hp2 HG01891.hp1 HG01934.hp2 others(18): Show |
intron_variant | MODIFIER | c.1364+352G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43990758 | ||||||
chr22:43990980
|
A | AT | 254 | a0001c0002t0001g0016a0001c0002t0001g0022a0001c0002t0001g0162others(251): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.1364+588dupT | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr22 | 43990980 | |||||
chr22:43990980
|
A | ATT | 9 | a0001c0002t0001g0189a0001c0004t0001g0171a0001c0006t0001g0101others(6): Show | 9 | HG01167.hp1 HG01169.hp2 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.1364+587_1364+588d others(4): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr22 | 43990980 | |||||
chr22:43991061
|
C | G | 1 | a0001c0007t0005g0034 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1364+655C>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43991061 | ||||||
chr22:43991186
|
C | G | 2 | a0001c0009t0001g0052a0001c0009t0001g0053 | 2 | HG01433.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1364+780C>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43991186 | ||||||
chr22:43991212
|
G | A | 1 | a0002c0001t0001g0196 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1364+806G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43991212 | ||||||
chr22:43991228
|
A | G | 186 | a0001c0002t0001g0016a0001c0002t0001g0022a0001c0002t0001g0161others(183): Show | 202 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.1364+822A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43991228 | ||||||
chr22:43991267
|
C | T | 1 | a0002c0001t0001g0199 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1364+861C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43991267 | ||||||
chr22:43991275
|
A | AT | 23 | a0001c0002t0002g0023a0001c0002t0002g0040a0001c0002t0002g0185others(20): Show | 24 | HG00438.hp2 HG00558.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.1364+890dupT | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr22 | 43991275 | |||||
chr22:43991275
|
AT | A | 8 | a0001c0002t0002g0300a0001c0002t0002g0301a0001c0002t0002g0309others(5): Show | 8 | HG00621.hp1 HG01070.hp1 HG01167.hp2 others(5): Show |
intron_variant | MODIFIER | c.1364+890delT | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr22 | 43991275 | |||||
chr22:43991324
|
C | G | 2 | a0001c0006t0001g0043a0001c0006t0001g0044 | 2 | HG02451.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1364+918C>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43991324 | ||||||
chr22:43991411
|
G | A | 3 | a0002c0001t0001g0214a0002c0001t0001g0227a0002c0001t0001g0238 | 3 | HG00639.hp2 HG00741.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.1364+1005G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43991411 | ||||||
chr22:43991418
|
C | T | 8 | a0001c0007t0001g0027a0001c0007t0001g0028a0001c0007t0001g0322others(5): Show | 10 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.1364+1012C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43991418 | ||||||
chr22:43991426
|
G | A | 1 | a0002c0001t0001g0229 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1364+1020G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43991426 | ||||||
chr22:43991501
|
C | G | 3 | a0002c0001t0001g0196a0002c0001t0001g0204a0002c0001t0001g0209 | 3 | HG01099.hp2 HG01261.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.1364+1095C>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43991501 | ||||||
chr22:43991837
|
CTCT | C | 3 | a0001c0008t0001g0033a0001c0008t0001g0179a0001c0008t0001g0180 | 3 | HG02257.hp1 HG02486.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1364+1436_1364+143 others(7): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr22 | 43991837 | |||||
chr22:43991873
|
C | T | 1 | a0002c0001t0001g0191 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1364+1467C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43991873 | ||||||
chr22:43992052
|
C | CTA | 187 | a0001c0002t0001g0016a0001c0002t0001g0022a0001c0002t0001g0161others(184): Show | 203 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.1364+1647_1364+164 others(6): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr22 | 43992052 | |||||
chr22:43992064
|
T | C | 5 | a0001c0008t0001g0033a0001c0008t0001g0176a0001c0008t0001g0177others(2): Show | 5 | HG01109.hp2 HG02109.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1364+1658T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43992064 | ||||||
chr22:43992116
|
G | C | 280 | a0001c0002t0001g0016a0001c0002t0001g0022a0001c0002t0001g0161others(277): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(302): Show |
intron_variant | MODIFIER | c.1364+1710G>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43992116 | ||||||
chr22:43992239
|
T | C | 6 | a0001c0002t0001g0016a0001c0002t0001g0163a0001c0002t0001g0165others(3): Show | 7 | HG01891.hp1 HG01934.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1364+1833T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43992239 | ||||||
chr22:43992328
|
C | T | 337 | a0001c0002t0001g0016a0001c0002t0001g0022a0001c0002t0001g0161others(334): Show | 376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.1364+1922C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43992328 | ||||||
chr22:43992366
|
G | A | 12 | a0001c0002t0001g0016a0001c0002t0001g0161a0001c0002t0001g0162others(9): Show | 13 | HG01891.hp1 HG01934.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.1364+1960G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43992366 | ||||||
chr22:43992367
|
C | T | 1 | a0002c0012t0001g0149 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1364+1961C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43992367 | ||||||
chr22:43992390
|
G | A | 1 | a0001c0002t0002g0314 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1364+1984G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43992390 | ||||||
chr22:43992401
|
G | T | 3 | a0001c0004t0001g0121a0001c0004t0001g0317a0001c0004t0001g0318 | 3 | HG01358.hp1 HG02602.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.1364+1995G>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43992401 | ||||||
chr22:43992438
|
G | A | 8 | a0001c0005t0001g0029a0001c0005t0001g0328a0001c0005t0001g0329others(5): Show | 9 | HG02055.hp2 HG02615.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1364+2032G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43992438 | ||||||
chr22:43992457
|
G | A | 81 | a0001c0004t0001g0002a0001c0004t0001g0005a0001c0004t0001g0013others(78): Show | 90 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.1364+2051G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43992457 | ||||||
chr22:43992537
|
A | G | 187 | a0001c0002t0001g0016a0001c0002t0001g0022a0001c0002t0001g0161others(184): Show | 203 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.1364+2131A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43992537 | ||||||
chr22:43992728
|
C | A | 3 | a0001c0008t0001g0033a0001c0008t0001g0179a0001c0008t0001g0180 | 3 | HG02257.hp1 HG02486.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1364+2322C>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43992728 | ||||||
chr22:43992797
|
G | A | 2 | a0001c0002t0004g0293a0001c0007t0005g0034 | 2 | HG03195.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1364+2391G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43992797 | ||||||
chr22:43992937
|
T | C | 97 | a0001c0002t0001g0337a0001c0002t0001g0338a0001c0002t0001g0339others(94): Show | 105 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.1364+2531T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43992937 | ||||||
chr22:43993017
|
A | G | 1 | a0001c0008t0001g0175 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1364+2611A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43993017 | ||||||
chr22:43993018
|
G | A | 1 | a0001c0002t0002g0314 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1364+2612G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43993018 | ||||||
chr22:43993039
|
A | G | 2 | a0003c0003t0001g0059a0003c0003t0001g0061 | 2 | HG01169.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.1364+2633A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43993039 | ||||||
chr22:43993085
|
G | A | 2 | a0001c0002t0001g0189a0001c0007t0001g0326 | 2 | HG03195.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1364+2679G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43993085 | ||||||
chr22:43993229
|
C | G | 1 | a0002c0001t0001g0195 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1364+2823C>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43993229 | ||||||
chr22:43993274
|
G | A | 8 | a0001c0002t0001g0022a0001c0002t0001g0265a0001c0002t0001g0266others(5): Show | 9 | HG00423.hp1 HG04204.hp1 NA18963.hp2 others(6): Show |
intron_variant | MODIFIER | c.1364+2868G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43993274 | ||||||
chr22:43993373
|
CGGCTTTT others(27): Show |
C | 1 | a0001c0006t0001g0043 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1365-2963_1365-293 others(38): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr22 | 43993373 | |||||
chr22:43993512
|
G | A | 58 | a0001c0002t0001g0022a0001c0002t0001g0189a0001c0002t0001g0265others(55): Show | 63 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.1365-2826G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43993512 | ||||||
chr22:43993520
|
C | T | 3 | a0001c0008t0001g0033a0001c0008t0001g0179a0001c0008t0001g0180 | 3 | HG02257.hp1 HG02486.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1365-2818C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43993520 | ||||||
chr22:43993634
|
T | C | 186 | a0001c0002t0001g0016a0001c0002t0001g0022a0001c0002t0001g0161others(183): Show | 202 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.1365-2704T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43993634 | ||||||
chr22:43993638
|
C | T | 6 | a0001c0002t0002g0274a0001c0002t0002g0300a0001c0002t0002g0304others(3): Show | 6 | HG00099.hp2 HG01070.hp1 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.1365-2700C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43993638 | ||||||
chr22:43993676
|
C | T | 1 | a0001c0002t0001g0188 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1365-2662C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43993676 | ||||||
chr22:43993914
|
G | A | 2 | a0001c0002t0002g0274a0001c0004t0001g0151 | 2 | HG02074.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.1365-2424G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43993914 | ||||||
chr22:43993929
|
C | T | 3 | a0001c0008t0001g0178a0001c0008t0001g0181a0001c0008t0001g0182 | 3 | HG02559.hp1 HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1365-2409C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43993929 | ||||||
chr22:43993982
|
C | T | 1 | a0002c0001t0001g0247 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1365-2356C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43993982 | ||||||
chr22:43994145
|
A | AGC | 3 | a0001c0010t0001g0124a0001c0010t0001g0136a0001c0010t0001g0145 | 3 | HG02615.hp1 HG02895.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1365-2192_1365-219 others(6): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr22 | 43994145 | |||||
chr22:43994168
|
G | A | 58 | a0001c0002t0001g0022a0001c0002t0001g0189a0001c0002t0001g0265others(55): Show | 63 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.1365-2170G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43994168 | ||||||
chr22:43994195
|
G | C | 1 | a0005c0019t0007g0236 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1365-2143G>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43994195 | ||||||
chr22:43994247
|
C | T | 1 | a0001c0002t0002g0289 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1365-2091C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43994247 | ||||||
chr22:43994341
|
GT | G | 12 | a0001c0002t0001g0016a0001c0002t0001g0161a0001c0002t0001g0162others(9): Show | 13 | HG01891.hp1 HG01934.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.1365-1996delT | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43994341 | ||||||
chr22:43994356
|
T | C | 277 | a0001c0002t0001g0016a0001c0002t0001g0022a0001c0002t0001g0161others(274): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(299): Show |
intron_variant | MODIFIER | c.1365-1982T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43994356 | ||||||
chr22:43994405
|
C | T | 2 | a0001c0004t0001g0132a0001c0004t0001g0143 | 2 | NA18953.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.1365-1933C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43994405 | ||||||
chr22:43994457
|
G | A | 1 | a0001c0006t0001g0264 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1365-1881G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43994457 | ||||||
chr22:43994475
|
T | G | 1 | a0001c0002t0001g0281 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1365-1863T>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43994475 | ||||||
chr22:43994486
|
A | G | 291 | a0001c0002t0001g0016a0001c0002t0001g0022a0001c0002t0001g0161others(288): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.1365-1852A>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43994486 | ||||||
chr22:43994666
|
C | T | 2 | a0001c0002t0004g0293a0001c0007t0005g0034 | 2 | HG03195.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1365-1672C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43994666 | ||||||
chr22:43994667
|
G | A | 71 | a0001c0004t0001g0002a0001c0004t0001g0005a0001c0004t0001g0013others(68): Show | 79 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.1365-1671G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43994667 | ||||||
chr22:43994688
|
C | T | 174 | a0001c0002t0001g0016a0001c0002t0001g0022a0001c0002t0001g0161others(171): Show | 188 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.1365-1650C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43994688 | ||||||
chr22:43995036
|
C | G | 1 | a0002c0001t0001g0217 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1365-1302C>G | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43995036 | ||||||
chr22:43995145
|
T | C | 292 | a0001c0002t0001g0016a0001c0002t0001g0022a0001c0002t0001g0161others(289): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(314): Show |
intron_variant | MODIFIER | c.1365-1193T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43995145 | ||||||
chr22:43995179
|
C | T | 3 | a0001c0002t0001g0337a0001c0002t0001g0338a0001c0002t0001g0339 | 3 | HG02647.hp1 HG02965.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1365-1159C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43995179 | ||||||
chr22:43995349
|
CAAGGGCA others(15): Show |
C | 2 | a0001c0002t0004g0293a0001c0007t0005g0034 | 2 | HG03195.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1365-984_1365-963d others(24): Show |
SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr22 | 43995349 | |||||
chr22:43995354
|
G | A | 93 | a0001c0002t0001g0337a0001c0002t0001g0338a0001c0002t0001g0339others(90): Show | 101 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.1365-984G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43995354 | ||||||
chr22:43995517
|
C | T | 12 | a0001c0005t0001g0029a0001c0005t0001g0155a0001c0005t0001g0328others(9): Show | 13 | HG02055.hp2 HG02615.hp2 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.1365-821C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43995517 | ||||||
chr22:43995708
|
T | C | 177 | a0001c0002t0001g0016a0001c0002t0001g0022a0001c0002t0001g0161others(174): Show | 191 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.1365-630T>C | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43995708 | ||||||
chr22:43995806
|
G | A | 111 | a0001c0002t0001g0016a0001c0002t0001g0161a0001c0002t0001g0162others(108): Show | 120 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.1365-532G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43995806 | ||||||
chr22:43995969
|
C | A | 1 | a0001c0008t0001g0181 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1365-369C>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43995969 | ||||||
chr22:43996049
|
G | A | 6 | a0001c0002t0001g0016a0001c0002t0001g0163a0001c0002t0001g0165others(3): Show | 7 | HG01891.hp1 HG01934.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1365-289G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43996049 | ||||||
chr22:43996189
|
G | A | 2 | a0001c0002t0004g0293a0001c0007t0005g0034 | 2 | HG03195.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1365-149G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43996189 | ||||||
chr22:43996223
|
G | A | 1 | a0003c0003t0001g0097 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1365-115G>A | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43996223 | ||||||
chr22:43996240
|
C | T | 1 | a0001c0002t0002g0305 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1365-98C>T | SAMM50 | ENSG00000100347.15 | transcript | ENST00000350028.5 | protein_coding | 14/14 | chr22 | 43996240 |