Item | Value |
---|---|
geneid | 90678 |
ensemblid | ENSG00000148356.15 |
hgncid | 25135 |
symbol | LRSAM1 |
name | leucine rich repeat and sterile alpha motif containing 1 |
refseq_nuc | NM_001005373.4 |
refseq_prot | NP_001005373.1 |
ensembl_nuc | ENST00000300417.11 |
ensembl_prot | ENSP00000300417.6 |
mane_status | MANE Select |
chr | chr9 |
start | 127451510 |
end | 127503499 |
strand | + |
ver | v1.2 |
region | chr9:127451510-127503499 |
region5000 | chr9:127446510-127508499 |
regionname0 | LRSAM1_chr9_127451510_127503499 |
regionname5000 | LRSAM1_chr9_127446510_127508499 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 723 | 219 | 41 | 46 | 96 | 12 | 23 | 74 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | copy fasta | chr9 | 127446510 | 127508499 |
a0002 | 1/0 | 723 | 102 | 32 | 19 | 35 | 4 | 11 | 29 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | copy fasta | chr9 | 127446510 | 127508499 |
a0003 | 0/0 | 723 | 9 | 9 | 0 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | copy fasta | chr9 | 127446510 | 127508499 |
a0004 | 0/0 | 723 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | copy fasta | chr9 | 127446510 | 127508499 |
a0005 | 0/0 | 723 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | copy fasta | chr9 | 127446510 | 127508499 |
a0006 | 0/0 | 723 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | copy fasta | chr9 | 127446510 | 127508499 |
a0007 | 0/0 | 723 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | copy fasta | chr9 | 127446510 | 127508499 |
a0008 | 0/0 | 723 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | copy fasta | chr9 | 127446510 | 127508499 |
a0009 | 0/0 | 723 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | copy fasta | chr9 | 127446510 | 127508499 |
a0010 | 0/0 | 723 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | copy fasta | chr9 | 127446510 | 127508499 |
a0011 | 0/0 | 723 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | copy fasta | chr9 | 127446510 | 127508499 |
chapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 2172 | 163 | 35 | 31 | 73 | 7 | 16 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | copy fasta | chr9 | 127446510 | 127508499 | |
c0002 | 1/0 | 2172 | 99 | 30 | 19 | 35 | 4 | 10 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | copy fasta | chr9 | 127446510 | 127508499 | |
c0003 | 0/0 | 2172 | 51 | 4 | 14 | 22 | 5 | 6 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | copy fasta | chr9 | 127446510 | 127508499 | |
c0004 | 0/0 | 2172 | 9 | 9 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | copy fasta | chr9 | 127446510 | 127508499 | |
c0005 | 0/0 | 2172 | 3 | 2 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | copy fasta | chr9 | 127446510 | 127508499 | |
c0006 | 0/0 | 2172 | 3 | 0 | 0 | 3 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | copy fasta | chr9 | 127446510 | 127508499 | |
c0007 | 0/0 | 2172 | 3 | 2 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | copy fasta | chr9 | 127446510 | 127508499 | |
c0008 | 0/0 | 2172 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | copy fasta | chr9 | 127446510 | 127508499 | |
c0009 | 0/0 | 2172 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | copy fasta | chr9 | 127446510 | 127508499 | |
c0010 | 0/0 | 2172 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | copy fasta | chr9 | 127446510 | 127508499 | |
c0011 | 0/0 | 2172 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | copy fasta | chr9 | 127446510 | 127508499 | |
c0012 | 0/0 | 2172 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | copy fasta | chr9 | 127446510 | 127508499 | |
c0013 | 0/0 | 2172 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | copy fasta | chr9 | 127446510 | 127508499 | |
c0014 | 0/0 | 2172 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | copy fasta | chr9 | 127446510 | 127508499 | |
c0015 | 0/0 | 2172 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | copy fasta | chr9 | 127446510 | 127508499 | |
c0016 | 0/0 | 2172 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | copy fasta | chr9 | 127446510 | 127508499 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 949 | 333 | 82 | 65 | 134 | 16 | 34 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | copy fasta | chr9 | 127446510 | 127508499 |
t0002 | 0/0 | 949 | 4 | 4 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | copy fasta | chr9 | 127446510 | 127508499 |
t0003 | 0/0 | 949 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | copy fasta | chr9 | 127446510 | 127508499 |
t0004 | 0/0 | 899 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | copy fasta | chr9 | 127446510 | 127508499 |
t0005 | 0/0 | 949 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | copy fasta | chr9 | 127446510 | 127508499 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0005 | 0/1 | 2 | 0 | 0 | 0 | 1 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0007 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0164 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0328 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0329 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 2172 | 163 | 35 | 31 | 73 | 7 | 16 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | copy fasta | chr9 | 127446510 | 127508499 | |
a0001c0003 | 0/0 | 2172 | 51 | 4 | 14 | 22 | 5 | 6 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | copy fasta | chr9 | 127446510 | 127508499 | |
a0001c0007 | 0/0 | 2172 | 3 | 2 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | copy fasta | chr9 | 127446510 | 127508499 | |
a0001c0013 | 0/0 | 2172 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | copy fasta | chr9 | 127446510 | 127508499 | |
a0001c0016 | 0/0 | 2172 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | copy fasta | chr9 | 127446510 | 127508499 | |
a0002c0002 | 1/0 | 2172 | 99 | 30 | 19 | 35 | 4 | 10 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | copy fasta | chr9 | 127446510 | 127508499 | |
a0002c0005 | 0/0 | 2172 | 3 | 2 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | copy fasta | chr9 | 127446510 | 127508499 | |
a0003c0004 | 0/0 | 2172 | 9 | 9 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | copy fasta | chr9 | 127446510 | 127508499 | |
a0004c0006 | 0/0 | 2172 | 3 | 0 | 0 | 3 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | copy fasta | chr9 | 127446510 | 127508499 | |
a0005c0012 | 0/0 | 2172 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | copy fasta | chr9 | 127446510 | 127508499 | |
a0006c0014 | 0/0 | 2172 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | copy fasta | chr9 | 127446510 | 127508499 | |
a0007c0011 | 0/0 | 2172 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | copy fasta | chr9 | 127446510 | 127508499 | |
a0008c0010 | 0/0 | 2172 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | copy fasta | chr9 | 127446510 | 127508499 | |
a0009c0009 | 0/0 | 2172 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | copy fasta | chr9 | 127446510 | 127508499 | |
a0010c0008 | 0/0 | 2172 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | copy fasta | chr9 | 127446510 | 127508499 | |
a0011c0015 | 0/0 | 2172 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | copy fasta | chr9 | 127446510 | 127508499 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 3120 | 162 | 34 | 31 | 73 | 7 | 16 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | copy fasta | chr9 | 127446510 | 127508499 |
a0001c0001t0002 | 0/0 | 3120 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | copy fasta | chr9 | 127446510 | 127508499 |
a0001c0003t0001 | 0/0 | 3120 | 51 | 4 | 14 | 22 | 5 | 6 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | copy fasta | chr9 | 127446510 | 127508499 |
a0001c0007t0001 | 0/0 | 3120 | 3 | 2 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | copy fasta | chr9 | 127446510 | 127508499 |
a0001c0013t0001 | 0/0 | 3120 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | copy fasta | chr9 | 127446510 | 127508499 |
a0001c0016t0001 | 0/0 | 3120 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | copy fasta | chr9 | 127446510 | 127508499 |
a0002c0002t0001 | 1/0 | 3120 | 97 | 30 | 18 | 34 | 4 | 10 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | copy fasta | chr9 | 127446510 | 127508499 |
a0002c0002t0003 | 0/0 | 3120 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | copy fasta | chr9 | 127446510 | 127508499 |
a0002c0002t0005 | 0/0 | 3120 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | copy fasta | chr9 | 127446510 | 127508499 |
a0002c0005t0001 | 0/0 | 3120 | 2 | 1 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | copy fasta | chr9 | 127446510 | 127508499 |
a0002c0005t0002 | 0/0 | 3120 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | copy fasta | chr9 | 127446510 | 127508499 |
a0003c0004t0001 | 0/0 | 3120 | 7 | 7 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | copy fasta | chr9 | 127446510 | 127508499 |
a0003c0004t0002 | 0/0 | 3120 | 2 | 2 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | copy fasta | chr9 | 127446510 | 127508499 |
a0004c0006t0001 | 0/0 | 3120 | 2 | 0 | 0 | 2 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | copy fasta | chr9 | 127446510 | 127508499 |
a0004c0006t0004 | 0/0 | 3070 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | copy fasta | chr9 | 127446510 | 127508499 |
a0005c0012t0001 | 0/0 | 3120 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | copy fasta | chr9 | 127446510 | 127508499 |
a0006c0014t0001 | 0/0 | 3120 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | copy fasta | chr9 | 127446510 | 127508499 |
a0007c0011t0001 | 0/0 | 3120 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | copy fasta | chr9 | 127446510 | 127508499 |
a0008c0010t0001 | 0/0 | 3120 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | copy fasta | chr9 | 127446510 | 127508499 |
a0009c0009t0001 | 0/0 | 3120 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | copy fasta | chr9 | 127446510 | 127508499 |
a0010c0008t0001 | 0/0 | 3120 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | copy fasta | chr9 | 127446510 | 127508499 |
a0011c0015t0001 | 0/0 | 3120 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | copy fasta | chr9 | 127446510 | 127508499 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0005 | 0/1 | 2 | 0 | 0 | 0 | 1 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0001t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0003t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0003t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0003t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0003t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0003t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0003t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0003t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0003t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0003t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0003t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0003t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0003t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0003t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0003t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0003t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0003t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0003t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0003t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0003t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0003t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0003t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0003t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0003t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0003t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0003t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0003t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0003t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0003t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0003t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0003t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0003t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0003t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0003t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0003t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0003t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0003t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0003t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0003t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0003t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0003t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0003t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0003t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0003t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0003t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0003t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0003t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0003t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0003t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0003t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0003t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0003t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0007t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0007t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0007t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0013t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0001c0016t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0164 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0002t0005g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0005t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0005t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0002c0005t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0003c0004t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0003c0004t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0003c0004t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0003c0004t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0003c0004t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0003c0004t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0003c0004t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0003c0004t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0003c0004t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0004c0006t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0004c0006t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0004c0006t0004g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0005c0012t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0006c0014t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0007c0011t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0008c0010t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0009c0009t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0010c0008t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
a0011c0015t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | GBR | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | GBR | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG00140 | hp1 | a0002 | c0002 | t0001 | g0042 | EUR | GBR | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG00140 | hp2 | a0001 | c0003 | t0001 | g0088 | EUR | GBR | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG00280 | hp1 | a0002 | c0002 | t0001 | g0177 | EUR | FIN | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG00280 | hp2 | a0002 | c0002 | t0001 | g0170 | EUR | FIN | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0266 | EUR | FIN | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG00323 | hp2 | a0001 | c0003 | t0001 | g0141 | EUR | FIN | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | CHS | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG00423 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | CHS | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG00438 | hp2 | a0002 | c0002 | t0001 | g0044 | EAS | CHS | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG00558 | hp1 | a0001 | c0003 | t0001 | g0080 | EAS | CHS | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | CHS | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | CHS | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG00609 | hp2 | a0001 | c0003 | t0001 | g0041 | EAS | CHS | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | CHS | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG00621 | hp2 | a0002 | c0002 | t0001 | g0155 | EAS | CHS | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0326 | AMR | PUR | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0315 | AMR | PUR | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG00673 | hp1 | a0001 | c0013 | t0001 | g0146 | EAS | CHS | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | CHS | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG00733 | hp2 | a0002 | c0002 | t0001 | g0045 | AMR | PUR | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0327 | AMR | PUR | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG00738 | hp2 | a0002 | c0002 | t0001 | g0053 | AMR | PUR | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG00741 | hp1 | a0001 | c0003 | t0001 | g0110 | AMR | PUR | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG00741 | hp2 | a0001 | c0003 | t0001 | g0096 | AMR | PUR | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG01070 | hp1 | a0001 | c0003 | t0001 | g0097 | AMR | PUR | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG01070 | hp2 | a0001 | c0003 | t0001 | g0105 | AMR | PUR | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | PUR | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG01071 | hp2 | a0001 | c0003 | t0001 | g0098 | AMR | PUR | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG01074 | hp1 | a0001 | c0003 | t0001 | g0101 | AMR | PUR | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG01081 | hp1 | a0001 | c0003 | t0001 | g0099 | AMR | PUR | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG01081 | hp2 | a0002 | c0002 | t0001 | g0169 | AMR | PUR | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG01099 | hp1 | a0001 | c0003 | t0001 | g0111 | AMR | PUR | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | PUR | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG01106 | hp1 | a0008 | c0010 | t0001 | g0054 | AMR | PUR | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0319 | AMR | PUR | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG01109 | hp1 | a0001 | c0007 | t0001 | g0278 | AMR | PUR | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG01109 | hp2 | a0002 | c0002 | t0001 | g0068 | AMR | PUR | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG01168 | hp1 | a0002 | c0002 | t0001 | g0172 | AMR | PUR | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG01169 | hp1 | a0002 | c0002 | t0001 | g0109 | AMR | PUR | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG01169 | hp2 | a0002 | c0002 | t0001 | g0049 | AMR | PUR | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG01175 | hp1 | a0002 | c0002 | t0001 | g0055 | AMR | PUR | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG01175 | hp2 | a0001 | c0003 | t0001 | g0152 | AMR | PUR | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG01192 | hp1 | a0002 | c0002 | t0005 | g0046 | AMR | PUR | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG01192 | hp2 | a0001 | c0003 | t0001 | g0074 | AMR | PUR | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG01255 | hp1 | a0001 | c0003 | t0001 | g0137 | AMR | CLM | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0302 | AMR | CLM | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG01256 | hp1 | a0002 | c0002 | t0001 | g0133 | AMR | CLM | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | CLM | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG01258 | hp1 | a0002 | c0002 | t0001 | g0158 | AMR | CLM | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG01258 | hp2 | a0002 | c0002 | t0001 | g0056 | AMR | CLM | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG01261 | hp1 | a0002 | c0002 | t0001 | g0106 | AMR | CLM | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | CLM | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0253 | AMR | CLM | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0279 | AMR | CLM | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | CLM | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG01358 | hp2 | a0002 | c0002 | t0001 | g0178 | AMR | CLM | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG01361 | hp1 | a0002 | c0002 | t0001 | g0157 | AMR | CLM | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0320 | AMR | CLM | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | CLM | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG01433 | hp2 | a0001 | c0003 | t0001 | g0156 | AMR | CLM | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG01496 | hp1 | a0002 | c0002 | t0001 | g0066 | AMR | CLM | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | CLM | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0329 | EUR | IBS | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG01515 | hp2 | a0001 | c0003 | t0001 | g0084 | EUR | IBS | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG01517 | hp1 | a0001 | c0003 | t0001 | g0083 | EUR | IBS | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0204 | EUR | IBS | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG01884 | hp1 | a0002 | c0002 | t0001 | g0104 | AFR | ACB | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG01884 | hp2 | a0003 | c0004 | t0001 | g0024 | AFR | ACB | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0292 | AMR | PEL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0306 | AMR | PEL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG01952 | hp1 | a0001 | c0003 | t0001 | g0127 | AMR | PEL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG01952 | hp2 | a0002 | c0002 | t0001 | g0052 | AMR | PEL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0305 | AMR | PEL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG01975 | hp2 | a0002 | c0002 | t0001 | g0047 | AMR | PEL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | PEL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PEL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | PEL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0309 | AMR | PEL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG01993 | hp1 | a0002 | c0002 | t0001 | g0048 | AMR | PEL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0297 | AMR | PEL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | PEL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG02004 | hp2 | a0001 | c0003 | t0001 | g0113 | AMR | PEL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG02015 | hp1 | a0001 | c0003 | t0001 | g0131 | EAS | KHV | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | KHV | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG02055 | hp1 | a0001 | c0003 | t0001 | g0173 | AFR | ACB | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG02055 | hp2 | a0003 | c0004 | t0002 | g0025 | AFR | ACB | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | KHV | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG02056 | hp2 | a0001 | c0003 | t0001 | g0043 | EAS | KHV | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | KHV | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG02083 | hp2 | a0001 | c0003 | t0001 | g0120 | EAS | KHV | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0332 | EAS | KHV | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | KHV | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG02132 | hp2 | a0002 | c0002 | t0001 | g0121 | EAS | KHV | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG02145 | hp1 | a0002 | c0002 | t0001 | g0058 | AFR | ACB | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | ACB | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | CDX | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | CDX | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | CDX | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG02165 | hp2 | a0002 | c0002 | t0001 | g0089 | EAS | CDX | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG02257 | hp1 | a0001 | c0003 | t0001 | g0100 | AFR | ACB | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG02257 | hp2 | a0002 | c0002 | t0001 | g0179 | AFR | ACB | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG02258 | hp1 | a0002 | c0002 | t0001 | g0036 | AFR | ACB | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | ACB | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG02280 | hp2 | a0002 | c0002 | t0001 | g0140 | AFR | ACB | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0261 | AFR | ACB | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG02451 | hp2 | a0003 | c0004 | t0001 | g0019 | AFR | ACB | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | KHV | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG02523 | hp2 | a0002 | c0002 | t0001 | g0034 | EAS | KHV | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG02572 | hp1 | a0002 | c0002 | t0001 | g0062 | AFR | GWD | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG02572 | hp2 | a0002 | c0002 | t0001 | g0091 | AFR | GWD | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0325 | SAS | PJL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG02602 | hp2 | a0002 | c0002 | t0001 | g0057 | SAS | PJL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG02615 | hp1 | a0002 | c0002 | t0001 | g0070 | AFR | GWD | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG02615 | hp2 | a0002 | c0002 | t0001 | g0075 | AFR | GWD | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | GWD | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG02622 | hp2 | a0002 | c0002 | t0001 | g0032 | AFR | GWD | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG02630 | hp1 | a0003 | c0004 | t0001 | g0029 | AFR | GWD | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0277 | AFR | GWD | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG02647 | hp1 | a0002 | c0002 | t0001 | g0151 | AFR | GWD | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | GWD | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0324 | SAS | PJL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG02683 | hp2 | a0002 | c0002 | t0001 | g0114 | SAS | PJL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0251 | SAS | PJL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG02698 | hp2 | a0001 | c0003 | t0001 | g0112 | SAS | PJL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | GWD | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | GWD | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG02723 | hp2 | a0001 | c0007 | t0001 | g0276 | AFR | GWD | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG02735 | hp1 | a0002 | c0002 | t0001 | g0081 | SAS | PJL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG02735 | hp2 | a0002 | c0005 | t0001 | g0215 | SAS | PJL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0248 | SAS | PJL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG02738 | hp2 | a0001 | c0003 | t0001 | g0153 | SAS | PJL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG02809 | hp1 | a0002 | c0002 | t0001 | g0037 | AFR | GWD | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG02818 | hp2 | a0002 | c0002 | t0001 | g0071 | AFR | GWD | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG02886 | hp2 | a0002 | c0002 | t0001 | g0154 | AFR | GWD | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | GWD | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG02895 | hp2 | a0003 | c0004 | t0001 | g0031 | AFR | GWD | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | GWD | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG02896 | hp2 | a0002 | c0002 | t0001 | g0003 | AFR | GWD | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG02897 | hp1 | a0002 | c0002 | t0001 | g0003 | AFR | GWD | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG02897 | hp2 | a0003 | c0004 | t0001 | g0030 | AFR | GWD | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | ESN | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG02922 | hp2 | a0010 | c0008 | t0001 | g0092 | AFR | ESN | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ESN | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG02976 | hp2 | a0003 | c0004 | t0001 | g0020 | AFR | ESN | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0322 | SAS | PJL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG03017 | hp2 | a0002 | c0002 | t0001 | g0128 | SAS | PJL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG03098 | hp1 | a0002 | c0002 | t0001 | g0035 | AFR | MSL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG03098 | hp2 | a0002 | c0002 | t0001 | g0166 | AFR | MSL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0286 | AFR | ESN | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG03130 | hp2 | a0002 | c0002 | t0001 | g0129 | AFR | ESN | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | ESN | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG03139 | hp2 | a0001 | c0007 | t0001 | g0275 | AFR | ESN | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG03195 | hp1 | a0005 | c0012 | t0001 | g0117 | AFR | ESN | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0260 | AFR | ESN | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG03239 | hp2 | a0001 | c0003 | t0001 | g0167 | SAS | PJL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | MSL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG03486 | hp1 | a0011 | c0015 | t0001 | g0102 | AFR | MSL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG03486 | hp2 | a0002 | c0005 | t0001 | g0018 | AFR | MSL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG03491 | hp2 | a0002 | c0002 | t0001 | g0168 | SAS | PJL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG03516 | hp1 | a0001 | c0001 | t0002 | g0027 | AFR | ESN | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | ESN | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG03540 | hp1 | a0002 | c0002 | t0001 | g0038 | AFR | GWD | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG03540 | hp2 | a0002 | c0002 | t0001 | g0060 | AFR | GWD | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG03579 | hp1 | a0007 | c0011 | t0001 | g0174 | AFR | MSL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG03579 | hp2 | a0002 | c0002 | t0001 | g0001 | AFR | MSL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | PJL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | PJL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG03831 | hp1 | a0002 | c0002 | t0001 | g0065 | SAS | BEB | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG03831 | hp2 | a0002 | c0002 | t0001 | g0061 | SAS | BEB | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG03834 | hp1 | a0001 | c0016 | t0001 | g0079 | SAS | BEB | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG03834 | hp2 | a0002 | c0002 | t0001 | g0050 | SAS | BEB | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG03927 | hp1 | a0002 | c0002 | t0001 | g0143 | SAS | BEB | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0205 | SAS | BEB | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG03942 | hp1 | a0002 | c0002 | t0001 | g0064 | SAS | BEB | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG03942 | hp2 | a0001 | c0003 | t0001 | g0078 | SAS | BEB | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0249 | SAS | BEB | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG04184 | hp2 | a0001 | c0003 | t0001 | g0125 | SAS | BEB | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0323 | SAS | STU | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG04228 | hp2 | a0001 | c0003 | t0001 | g0040 | SAS | STU | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA18522 | hp1 | a0003 | c0004 | t0001 | g0015 | AFR | YRI | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA18522 | hp2 | a0002 | c0002 | t0001 | g0093 | AFR | YRI | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | YRI | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA18906 | hp2 | a0002 | c0002 | t0001 | g0001 | AFR | YRI | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA18942 | hp2 | a0001 | c0003 | t0001 | g0090 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA18943 | hp1 | a0002 | c0002 | t0001 | g0147 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA18944 | hp1 | a0002 | c0002 | t0001 | g0148 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA18944 | hp2 | a0001 | c0003 | t0001 | g0011 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA18945 | hp1 | a0001 | c0003 | t0001 | g0118 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA18946 | hp2 | a0002 | c0002 | t0001 | g0072 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA18948 | hp1 | a0002 | c0002 | t0001 | g0119 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA18952 | hp1 | a0001 | c0003 | t0001 | g0115 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA18952 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA18956 | hp1 | a0002 | c0002 | t0001 | g0039 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA18957 | hp2 | a0002 | c0002 | t0001 | g0134 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA18971 | hp1 | a0001 | c0003 | t0001 | g0144 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA18973 | hp1 | a0002 | c0002 | t0001 | g0108 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA18973 | hp2 | a0001 | c0003 | t0001 | g0107 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA18974 | hp1 | a0002 | c0002 | t0001 | g0067 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA18974 | hp2 | a0004 | c0006 | t0004 | g0009 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA18975 | hp2 | a0001 | c0003 | t0001 | g0136 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA18978 | hp2 | a0001 | c0003 | t0001 | g0160 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA18979 | hp2 | a0002 | c0002 | t0001 | g0077 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA18980 | hp1 | a0001 | c0003 | t0001 | g0130 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA18982 | hp1 | a0002 | c0002 | t0001 | g0135 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA18984 | hp1 | a0001 | c0003 | t0001 | g0094 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA18989 | hp1 | a0004 | c0006 | t0001 | g0331 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA18991 | hp1 | a0002 | c0002 | t0001 | g0076 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA18997 | hp2 | a0001 | c0003 | t0001 | g0159 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA18998 | hp2 | a0002 | c0002 | t0001 | g0124 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA18999 | hp2 | a0002 | c0002 | t0001 | g0138 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA19000 | hp1 | a0001 | c0003 | t0001 | g0176 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA19001 | hp2 | a0009 | c0009 | t0001 | g0095 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA19002 | hp2 | a0002 | c0002 | t0001 | g0161 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA19004 | hp1 | a0002 | c0002 | t0001 | g0116 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA19007 | hp2 | a0002 | c0002 | t0001 | g0122 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA19012 | hp1 | a0001 | c0003 | t0001 | g0087 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA19012 | hp2 | a0002 | c0002 | t0001 | g0126 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA19030 | hp1 | a0002 | c0002 | t0001 | g0180 | AFR | LWK | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | LWK | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | LWK | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | LWK | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA19056 | hp1 | a0001 | c0003 | t0001 | g0073 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA19057 | hp1 | a0002 | c0002 | t0001 | g0145 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA19064 | hp1 | a0006 | c0014 | t0001 | g0234 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA19064 | hp2 | a0002 | c0002 | t0001 | g0175 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA19066 | hp2 | a0002 | c0002 | t0001 | g0149 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA19070 | hp2 | a0002 | c0002 | t0001 | g0142 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA19074 | hp2 | a0001 | c0003 | t0001 | g0132 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA19075 | hp1 | a0002 | c0002 | t0003 | g0171 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA19078 | hp2 | a0001 | c0003 | t0001 | g0033 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA19079 | hp1 | a0002 | c0002 | t0001 | g0163 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA19079 | hp2 | a0001 | c0003 | t0001 | g0086 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA19080 | hp1 | a0002 | c0002 | t0001 | g0123 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA19081 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA19083 | hp1 | a0002 | c0002 | t0001 | g0139 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA19088 | hp1 | a0004 | c0006 | t0001 | g0333 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA19088 | hp2 | a0002 | c0002 | t0001 | g0085 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA19240 | hp1 | a0002 | c0002 | t0001 | g0069 | AFR | YRI | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | YRI | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA20129 | hp1 | a0002 | c0002 | t0001 | g0059 | AFR | ASW | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA20129 | hp2 | a0001 | c0003 | t0001 | g0010 | AFR | ASW | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0230 | EUR | TSI | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0328 | EUR | TSI | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA20805 | hp1 | a0002 | c0002 | t0001 | g0051 | EUR | TSI | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA20805 | hp2 | a0001 | c0003 | t0001 | g0082 | EUR | TSI | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | GIH | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0293 | SAS | GIH | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG02109 | hp1 | a0002 | c0002 | t0001 | g0103 | AFR | ACB | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG02486 | hp1 | a0002 | c0002 | t0001 | g0063 | AFR | ACB | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | ACB | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG03471 | hp1 | a0002 | c0002 | t0001 | g0150 | AFR | MSL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG06807 | hp1 | a0003 | c0004 | t0002 | g0026 | AFR | USA | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
HG06807 | hp2 | a0001 | c0003 | t0001 | g0165 | AFR | USA | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA18955 | hp2 | a0002 | c0002 | t0001 | g0162 | EAS | JPT | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA20300 | hp1 | a0002 | c0005 | t0002 | g0028 | AFR | USA | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | USA | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0005 | REF | REF | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
homoSapiens_grch38 | hp1 | a0002 | c0002 | t0001 | g0164 | REF | REF | LRSAM1_chr9_127446510_127508499 | LRSAM1 | chr9 | 127446510 | 127508499 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:127454589 | A | G | 1 | a0011 | 1 | HG03486.hp1 | missense_variant | MODERATE | c.62A>G | p.Gln21Arg | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 3/26 | 410/3120 | 62/2172 | 21/723 | chr9 | 127454589 | ||
chr9:127467759 | C | T | 1 | a0003 | 9 | HG01884.hp2 HG02055.hp2 HG02451.hp2 others(6): Show |
missense_variant | MODERATE | c.548C>T | p.Ser183Leu | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/26 | 896/3120 | 548/2172 | 183/723 | chr9 | 127467759 | ||
chr9:127473897 | C | G | 1 | a0005 | 1 | HG03195.hp1 | missense_variant | MODERATE | c.716C>G | p.Thr239Arg | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/26 | 1064/3120 | 716/2172 | 239/723 | chr9 | 127473897 | ||
chr9:127479852 | T | G | 1 | a0010 | 1 | HG02922.hp2 | missense_variant | MODERATE | c.917T>G | p.Leu306Arg | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 14/26 | 1265/3120 | 917/2172 | 306/723 | chr9 | 127479852 | ||
chr9:127479887 | A | G | 5 | a0001a0003a0004others(2): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(230): Show |
missense_variant | MODERATE | c.952A>G | p.Asn318Asp | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 14/26 | 1300/3120 | 952/2172 | 318/723 | chr9 | 127479887 | ||
chr9:127489447 | G | A | 1 | a0009 | 1 | NA19001.hp2 | missense_variant | MODERATE | c.1351G>A | p.Ala451Thr | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 19/26 | 1699/3120 | 1351/2172 | 451/723 | chr9 | 127489447 | ||
chr9:127489478 | A | T | 1 | a0006 | 1 | NA19064.hp1 | missense_variant | MODERATE | c.1382A>T | p.Gln461Leu | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 19/26 | 1730/3120 | 1382/2172 | 461/723 | chr9 | 127489478 | ||
chr9:127489502 | G | A | 1 | a0007 | 1 | HG03579.hp1 | missense_variant | MODERATE | c.1406G>A | p.Arg469Gln | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 19/26 | 1754/3120 | 1406/2172 | 469/723 | chr9 | 127489502 | ||
chr9:127501072 | G | A | 1 | a0004 | 3 | NA18974.hp2 NA18989.hp1 NA19088.hp1 |
missense_variant | MODERATE | c.1975G>A | p.Val659Met | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 25/26 | 2323/3120 | 1975/2172 | 659/723 | chr9 | 127501072 | ||
chr9:127501139 | G | A | 1 | a0008 | 1 | HG01106.hp1 | missense_variant | MODERATE | c.2042G>A | p.Arg681Gln | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 25/26 | 2390/3120 | 2042/2172 | 681/723 | chr9 | 127501139 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:127454536 | C | T | 1 | a0001c0016 | 1 | HG03834.hp1 | synonymous_variant | LOW | c.9C>T | p.Leu3Leu | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 3/26 | 357/3120 | 9/2172 | 3/723 | chr9 | 127454536 | ||
chr9:127457390 | C | T | 6 | a0001c0001a0001c0007a0002c0005others(3): Show | 182 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(179): Show |
synonymous_variant | LOW | c.249C>T | p.Ile83Ile | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 6/26 | 597/3120 | 249/2172 | 83/723 | chr9 | 127457390 | ||
chr9:127462325 | C | T | 1 | a0001c0013 | 1 | HG00673.hp1 | synonymous_variant | LOW | c.480C>T | p.Asn160Asn | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/26 | 828/3120 | 480/2172 | 160/723 | chr9 | 127462325 | ||
chr9:127502884 | C | T | 1 | a0001c0007 | 3 | HG01109.hp1 HG02723.hp2 HG03139.hp2 |
synonymous_variant | LOW | c.2157C>T | p.Ile719Ile | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 26/26 | 2505/3120 | 2157/2172 | 719/723 | chr9 | 127502884 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:127451542 | C | T | 3 | a0001c0001t0002a0002c0005t0002a0003c0004t0002 | 4 | HG02055.hp2 HG03516.hp1 HG06807.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-316C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 1/26 | 2986 | chr9 | 127451542 | |||||
chr9:127451550 | G | A | 1 | a0002c0002t0003 | 1 | NA19075.hp1 | 5_prime_UTR_variant | MODIFIER | c.-308G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 1/26 | 2978 | chr9 | 127451550 | |||||
chr9:127452034 | GGGTGCAC others(396): Show |
G | 1 | a0004c0006t0004 | 1 | NA18974.hp2 | splice_donor_variant&splice_region_variant&5_prime_UTR_variant&intron_variant | HIGH | c.-80_-33+355del | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 2/26 | 2089 | INFO_REALIGN_3_PRIME | chr9 | 127452034 | ||||
chr9:127502956 | G | A | 1 | a0002c0002t0005 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*57G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 26/26 | 57 | chr9 | 127502956 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:127451684 | G | A | 1 | a0002c0002t0001g0008 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-189+15G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 1/25 | chr9 | 127451684 | ||||||
chr9:127452135 | C | T | 57 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0279others(54): Show | 59 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.-33+51C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 2/25 | chr9 | 127452135 | ||||||
chr9:127452325 | T | C | 1 | a0001c0003t0001g0010 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-33+241T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 2/25 | chr9 | 127452325 | ||||||
chr9:127452325 | T | TG | 57 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0279others(54): Show | 59 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.-33+246dupG | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr9 | 127452325 | |||||
chr9:127452529 | G | T | 4 | a0001c0001t0001g0277a0001c0007t0001g0275a0001c0007t0001g0276others(1): Show | 4 | HG01109.hp1 HG02630.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.-33+445G>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 2/25 | chr9 | 127452529 | ||||||
chr9:127452644 | G | A | 1 | a0001c0003t0001g0011 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-33+560G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 2/25 | chr9 | 127452644 | ||||||
chr9:127452970 | C | T | 96 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0181others(93): Show | 98 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.-33+886C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 2/25 | chr9 | 127452970 | ||||||
chr9:127453000 | G | A | 178 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(175): Show | 182 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.-33+916G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 2/25 | chr9 | 127453000 | ||||||
chr9:127453071 | C | CTTTA | 4 | a0001c0001t0001g0277a0001c0007t0001g0275a0001c0007t0001g0276others(1): Show | 4 | HG01109.hp1 HG02630.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.-33+1002_-33+1005d others(6): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr9 | 127453071 | |||||
chr9:127453238 | C | T | 1 | a0002c0002t0001g0180 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-33+1154C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 2/25 | chr9 | 127453238 | ||||||
chr9:127453432 | C | CT | 178 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(175): Show | 182 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.-32-1064_-32-1063i others(3): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 2/25 | chr9 | 127453432 | ||||||
chr9:127453517 | T | A | 1 | a0001c0001t0001g0279 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-32-979T>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 2/25 | chr9 | 127453517 | ||||||
chr9:127453571 | G | A | 1 | a0002c0002t0001g0032 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-32-925G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 2/25 | chr9 | 127453571 | ||||||
chr9:127453647 | T | C | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-32-849T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 2/25 | chr9 | 127453647 | ||||||
chr9:127453841 | G | T | 96 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0181others(93): Show | 98 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.-32-655G>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 2/25 | chr9 | 127453841 | ||||||
chr9:127453975 | C | T | 3 | a0002c0002t0001g0177a0002c0002t0001g0178a0002c0002t0001g0179 | 3 | HG00280.hp1 HG01358.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.-32-521C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 2/25 | chr9 | 127453975 | ||||||
chr9:127454047 | A | ATAGAAAG others(28): Show |
82 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(79): Show | 84 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.-32-427_-32-426ins others(35): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr9 | 127454047 | |||||
chr9:127454106 | C | T | 1 | a0001c0001t0001g0274 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-32-390C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 2/25 | chr9 | 127454106 | ||||||
chr9:127454644 | C | T | 1 | a0001c0001t0001g0273 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.72+45C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 3/25 | chr9 | 127454644 | ||||||
chr9:127454672 | G | T | 85 | a0001c0001t0001g0005a0001c0001t0001g0191a0001c0001t0001g0192others(82): Show | 86 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.72+73G>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 3/25 | chr9 | 127454672 | ||||||
chr9:127454771 | C | G | 73 | a0001c0001t0001g0005a0001c0001t0001g0203a0001c0001t0001g0204others(70): Show | 74 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.72+172C>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 3/25 | chr9 | 127454771 | ||||||
chr9:127454968 | A | C | 19 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0016others(16): Show | 19 | HG01884.hp2 HG02055.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.73-30A>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 3/25 | chr9 | 127454968 | ||||||
chr9:127455172 | G | A | 1 | a0001c0001t0001g0280 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.129+118G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 4/25 | chr9 | 127455172 | ||||||
chr9:127455182 | C | T | 4 | a0001c0001t0001g0277a0001c0007t0001g0275a0001c0007t0001g0276others(1): Show | 4 | HG01109.hp1 HG02630.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.129+128C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 4/25 | chr9 | 127455182 | ||||||
chr9:127455238 | C | T | 1 | a0001c0003t0001g0176 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.129+184C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 4/25 | chr9 | 127455238 | ||||||
chr9:127455247 | C | CA | 4 | a0001c0001t0001g0277a0001c0007t0001g0275a0001c0007t0001g0276others(1): Show | 4 | HG01109.hp1 HG02630.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.129+195dupA | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr9 | 127455247 | |||||
chr9:127455382 | A | G | 1 | a0002c0002t0001g0175 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.130-194A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 4/25 | chr9 | 127455382 | ||||||
chr9:127456015 | G | A | 1 | a0001c0003t0001g0033 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.174+395G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 5/25 | chr9 | 127456015 | ||||||
chr9:127456057 | C | T | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.174+437C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 5/25 | chr9 | 127456057 | ||||||
chr9:127456093 | G | T | 82 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(79): Show | 84 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.174+473G>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 5/25 | chr9 | 127456093 | ||||||
chr9:127456116 | C | G | 2 | a0001c0001t0001g0271a0001c0001t0001g0272 | 2 | HG00423.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.174+496C>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 5/25 | chr9 | 127456116 | ||||||
chr9:127456162 | C | CA | 6 | a0002c0002t0001g0034a0002c0002t0001g0035a0002c0002t0001g0036others(3): Show | 6 | HG02258.hp1 HG02523.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.174+562dupA | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr9 | 127456162 | |||||
chr9:127456162 | CA | C | 23 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0016others(20): Show | 23 | HG00735.hp2 HG01168.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.174+562delA | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr9 | 127456162 | |||||
chr9:127456162 | CAA | C | 150 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(147): Show | 154 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.174+561_174+562del others(2): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr9 | 127456162 | |||||
chr9:127456162 | CAAA | C | 9 | a0001c0001t0001g0190a0001c0001t0001g0202a0001c0001t0001g0277others(6): Show | 9 | HG01109.hp1 HG02129.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.174+560_174+562del others(3): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr9 | 127456162 | |||||
chr9:127456234 | G | GT | 6 | a0001c0001t0001g0267a0001c0001t0001g0268a0001c0001t0001g0269others(3): Show | 6 | HG00609.hp1 HG00621.hp1 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.174+629dupT | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr9 | 127456234 | |||||
chr9:127456259 | C | T | 11 | a0001c0001t0001g0004a0001c0001t0001g0181a0001c0001t0001g0182others(8): Show | 12 | HG02129.hp2 NA18950.hp1 NA18955.hp1 others(9): Show |
intron_variant | MODIFIER | c.174+639C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 5/25 | chr9 | 127456259 | ||||||
chr9:127456412 | T | TTAG | 180 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(177): Show | 184 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.174+793_174+795dup others(3): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr9 | 127456412 | |||||
chr9:127456426 | T | C | 1 | a0001c0003t0001g0040 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.174+806T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 5/25 | chr9 | 127456426 | ||||||
chr9:127456448 | C | G | 58 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0279others(55): Show | 60 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.174+828C>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 5/25 | chr9 | 127456448 | ||||||
chr9:127456523 | G | A | 15 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0016others(12): Show | 15 | HG01884.hp2 HG02258.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.175-793G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 5/25 | chr9 | 127456523 | ||||||
chr9:127456670 | C | T | 2 | a0002c0002t0001g0169a0002c0002t0001g0170 | 2 | HG00280.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.175-646C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 5/25 | chr9 | 127456670 | ||||||
chr9:127456766 | C | T | 19 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0016others(16): Show | 19 | HG01884.hp2 HG02055.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.175-550C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 5/25 | chr9 | 127456766 | ||||||
chr9:127456779 | T | A | 1 | a0002c0002t0001g0039 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.175-537T>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 5/25 | chr9 | 127456779 | ||||||
chr9:127456865 | CA | C | 8 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0201others(5): Show | 9 | HG00323.hp1 HG02896.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.175-436delA | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr9 | 127456865 | |||||
chr9:127456873 | A | C | 1 | a0001c0001t0001g0189 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.175-443A>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 5/25 | chr9 | 127456873 | ||||||
chr9:127456878 | A | T | 9 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(6): Show | 9 | HG01884.hp2 HG02451.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.175-438A>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 5/25 | chr9 | 127456878 | ||||||
chr9:127457130 | G | T | 58 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0279others(55): Show | 60 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.175-186G>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 5/25 | chr9 | 127457130 | ||||||
chr9:127457443 | C | A | 2 | a0001c0003t0001g0173a0007c0011t0001g0174 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.252+50C>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 6/25 | chr9 | 127457443 | ||||||
chr9:127457444 | G | A | 4 | a0001c0001t0001g0277a0001c0007t0001g0275a0001c0007t0001g0276others(1): Show | 4 | HG01109.hp1 HG02630.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.252+51G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 6/25 | chr9 | 127457444 | ||||||
chr9:127457464 | T | C | 181 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(178): Show | 185 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.252+71T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 6/25 | chr9 | 127457464 | ||||||
chr9:127457704 | G | C | 1 | a0001c0001t0001g0204 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.252+311G>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 6/25 | chr9 | 127457704 | ||||||
chr9:127457711 | G | C | 178 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(175): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.252+318G>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 6/25 | chr9 | 127457711 | ||||||
chr9:127457857 | C | T | 8 | a0001c0001t0001g0258a0001c0001t0001g0259a0001c0001t0001g0260others(5): Show | 8 | HG01099.hp2 HG02280.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.252+464C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 6/25 | chr9 | 127457857 | ||||||
chr9:127457898 | T | G | 1 | a0001c0003t0001g0043 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.252+505T>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 6/25 | chr9 | 127457898 | ||||||
chr9:127457932 | A | G | 9 | a0001c0001t0001g0007a0001c0001t0001g0322a0001c0001t0001g0323others(6): Show | 10 | HG00099.hp1 HG00639.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.252+539A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 6/25 | chr9 | 127457932 | ||||||
chr9:127457963 | T | G | 2 | a0001c0003t0001g0173a0007c0011t0001g0174 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.252+570T>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 6/25 | chr9 | 127457963 | ||||||
chr9:127457968 | C | CT | 98 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0013others(95): Show | 99 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.252+589dupT | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 127457968 | |||||
chr9:127458072 | G | A | 2 | a0001c0003t0001g0173a0007c0011t0001g0174 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.252+679G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 6/25 | chr9 | 127458072 | ||||||
chr9:127458090 | A | G | 1 | a0001c0001t0001g0257 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.252+697A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 6/25 | chr9 | 127458090 | ||||||
chr9:127458205 | A | T | 6 | a0001c0001t0001g0277a0001c0003t0001g0173a0001c0007t0001g0275others(3): Show | 6 | HG01109.hp1 HG02055.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.253-798A>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 6/25 | chr9 | 127458205 | ||||||
chr9:127458314 | G | A | 2 | a0002c0002t0001g0034a0002c0002t0001g0044 | 2 | HG00438.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.253-689G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 6/25 | chr9 | 127458314 | ||||||
chr9:127458359 | G | A | 20 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0016others(17): Show | 20 | HG01884.hp2 HG02055.hp2 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.253-644G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 6/25 | chr9 | 127458359 | ||||||
chr9:127458367 | C | T | 2 | a0001c0001t0001g0255a0001c0001t0001g0256 | 2 | HG02145.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.253-636C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 6/25 | chr9 | 127458367 | ||||||
chr9:127458368 | G | A | 2 | a0001c0003t0001g0173a0007c0011t0001g0174 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.253-635G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 6/25 | chr9 | 127458368 | ||||||
chr9:127458382 | T | C | 330 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(327): Show | 337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.253-621T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 6/25 | chr9 | 127458382 | ||||||
chr9:127458384 | G | A | 26 | a0002c0002t0001g0035a0002c0002t0001g0042a0002c0002t0001g0045others(23): Show | 26 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(23): Show |
intron_variant | MODIFIER | c.253-619G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 6/25 | chr9 | 127458384 | ||||||
chr9:127458388 | C | CA | 17 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0017others(14): Show | 18 | HG00438.hp1 HG02129.hp2 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.253-610dupA | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 127458388 | |||||
chr9:127458393 | AC | A | 3 | a0001c0001t0001g0206a0001c0001t0001g0207a0007c0011t0001g0174 | 3 | HG00639.hp2 HG03579.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.253-609delC | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 6/25 | chr9 | 127458393 | ||||||
chr9:127458394 | C | A | 177 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(174): Show | 181 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.253-609C>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 6/25 | chr9 | 127458394 | ||||||
chr9:127458399 | C | A | 180 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(177): Show | 184 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.253-604C>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 6/25 | chr9 | 127458399 | ||||||
chr9:127458404 | C | A | 25 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0016others(22): Show | 25 | HG00639.hp2 HG01884.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.253-599C>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 6/25 | chr9 | 127458404 | ||||||
chr9:127458417 | A | C | 176 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(173): Show | 180 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.253-586A>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 6/25 | chr9 | 127458417 | ||||||
chr9:127458419 | C | A | 178 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(175): Show | 182 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.253-584C>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 6/25 | chr9 | 127458419 | ||||||
chr9:127458424 | A | C | 1 | a0002c0002t0001g0163 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.253-579A>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 6/25 | chr9 | 127458424 | ||||||
chr9:127458439 | G | A | 19 | a0002c0002t0001g0042a0002c0002t0001g0045a0002c0002t0001g0047others(16): Show | 19 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(16): Show |
intron_variant | MODIFIER | c.253-564G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 6/25 | chr9 | 127458439 | ||||||
chr9:127458600 | A | T | 85 | a0001c0001t0001g0005a0001c0001t0001g0191a0001c0001t0001g0192others(82): Show | 86 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.253-403A>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 6/25 | chr9 | 127458600 | ||||||
chr9:127458677 | G | A | 180 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(177): Show | 184 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.253-326G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 6/25 | chr9 | 127458677 | ||||||
chr9:127458905 | G | A | 2 | a0003c0004t0002g0025a0003c0004t0002g0026 | 2 | HG02055.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.253-98G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 6/25 | chr9 | 127458905 | ||||||
chr9:127458986 | G | T | 1 | a0001c0001t0001g0186 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.253-17G>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 6/25 | chr9 | 127458986 | ||||||
chr9:127459109 | T | C | 180 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(177): Show | 184 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.321+38T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 7/25 | chr9 | 127459109 | ||||||
chr9:127459172 | A | T | 1 | a0002c0002t0001g0063 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.321+101A>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 7/25 | chr9 | 127459172 | ||||||
chr9:127459217 | G | GT | 114 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0185others(111): Show | 115 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.321+163dupT | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr9 | 127459217 | |||||
chr9:127459217 | G | GTT | 18 | a0001c0001t0001g0200a0001c0001t0001g0205a0001c0001t0001g0245others(15): Show | 18 | HG00423.hp1 HG00642.hp2 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.321+162_321+163dup others(2): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr9 | 127459217 | |||||
chr9:127459240 | A | C | 1 | a0001c0001t0001g0244 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.321+169A>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 7/25 | chr9 | 127459240 | ||||||
chr9:127459253 | G | A | 82 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(79): Show | 84 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.321+182G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 7/25 | chr9 | 127459253 | ||||||
chr9:127459419 | T | A | 178 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(175): Show | 182 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.321+348T>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 7/25 | chr9 | 127459419 | ||||||
chr9:127459455 | G | GT | 4 | a0001c0001t0001g0332a0004c0006t0001g0331a0004c0006t0001g0333others(1): Show | 4 | HG02129.hp1 NA18974.hp2 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.321+386dupT | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr9 | 127459455 | |||||
chr9:127459760 | T | C | 1 | a0002c0002t0001g0066 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.321+689T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 7/25 | chr9 | 127459760 | ||||||
chr9:127459933 | T | A | 1 | a0001c0001t0001g0286 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.321+862T>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 7/25 | chr9 | 127459933 | ||||||
chr9:127460093 | G | A | 1 | a0001c0001t0001g0014 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.321+1022G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 7/25 | chr9 | 127460093 | ||||||
chr9:127460173 | A | G | 178 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(175): Show | 182 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.322-1000A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 7/25 | chr9 | 127460173 | ||||||
chr9:127460174 | T | C | 1 | a0002c0002t0001g0067 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.322-999T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 7/25 | chr9 | 127460174 | ||||||
chr9:127460287 | C | T | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.322-886C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 7/25 | chr9 | 127460287 | ||||||
chr9:127460339 | A | G | 332 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(329): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.322-834A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 7/25 | chr9 | 127460339 | ||||||
chr9:127460348 | C | G | 1 | a0001c0001t0001g0186 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.322-825C>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 7/25 | chr9 | 127460348 | ||||||
chr9:127460451 | C | T | 2 | a0002c0002t0001g0149a0002c0002t0001g0162 | 2 | NA18955.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.322-722C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 7/25 | chr9 | 127460451 | ||||||
chr9:127460480 | C | G | 1 | a0001c0001t0001g0243 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.322-693C>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 7/25 | chr9 | 127460480 | ||||||
chr9:127460544 | C | A | 12 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(9): Show | 12 | HG02486.hp2 HG02717.hp2 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.322-629C>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 7/25 | chr9 | 127460544 | ||||||
chr9:127460636 | C | G | 1 | a0002c0002t0001g0148 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.322-537C>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 7/25 | chr9 | 127460636 | ||||||
chr9:127460769 | G | A | 1 | a0001c0001t0001g0014 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.322-404G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 7/25 | chr9 | 127460769 | ||||||
chr9:127460773 | G | A | 4 | a0001c0001t0001g0012a0001c0001t0001g0013a0002c0005t0001g0018others(1): Show | 4 | HG03041.hp1 HG03471.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.322-400G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 7/25 | chr9 | 127460773 | ||||||
chr9:127460790 | G | A | 5 | a0001c0001t0001g0285a0001c0001t0001g0287a0001c0001t0001g0288others(2): Show | 5 | NA18959.hp1 NA18979.hp1 NA19057.hp2 others(2): Show |
intron_variant | MODIFIER | c.322-383G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 7/25 | chr9 | 127460790 | ||||||
chr9:127460847 | C | CT | 25 | a0001c0001t0001g0004a0001c0001t0001g0182a0001c0001t0001g0183others(22): Show | 26 | HG00323.hp1 HG00323.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.322-300dupT | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr9 | 127460847 | |||||
chr9:127460847 | C | CTT | 49 | a0001c0001t0001g0005a0001c0001t0001g0181a0001c0001t0001g0187others(46): Show | 50 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.322-301_322-300dup others(2): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr9 | 127460847 | |||||
chr9:127460847 | C | CTTT | 78 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(75): Show | 80 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.322-302_322-300dup others(3): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr9 | 127460847 | |||||
chr9:127460847 | C | CTTTT | 24 | a0001c0001t0001g0013a0001c0001t0001g0023a0001c0001t0001g0254others(21): Show | 24 | HG00639.hp1 HG00735.hp1 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.322-303_322-300dup others(4): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr9 | 127460847 | |||||
chr9:127460847 | C | CTTTTTTT others(2592): Show |
1 | a0001c0001t0001g0232 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.322-300_322-299ins others(2599): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr9 | 127460847 | |||||
chr9:127460847 | CTTTTTTT others(3): Show |
C | 11 | a0001c0001t0001g0258a0002c0002t0001g0001a0002c0002t0001g0036others(8): Show | 12 | HG01109.hp2 HG02258.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.322-309_322-300del others(10): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr9 | 127460847 | |||||
chr9:127460847 | CTTTTTTT others(4): Show |
C | 1 | a0001c0003t0001g0033 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.322-310_322-300del others(11): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr9 | 127460847 | |||||
chr9:127460872 | T | C | 4 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(1): Show | 4 | HG02886.hp1 HG03041.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.322-301T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 7/25 | chr9 | 127460872 | ||||||
chr9:127460872 | T | TC | 8 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(5): Show | 8 | HG02486.hp2 HG02717.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.322-301_322-300ins others(1): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 7/25 | chr9 | 127460872 | ||||||
chr9:127460904 | G | A | 12 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(9): Show | 12 | HG02486.hp2 HG02717.hp2 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.322-269G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 7/25 | chr9 | 127460904 | ||||||
chr9:127461122 | G | A | 1 | a0001c0001t0001g0277 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.322-51G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 7/25 | chr9 | 127461122 | ||||||
chr9:127461136 | A | G | 1 | a0001c0001t0001g0232 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.322-37A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 7/25 | chr9 | 127461136 | ||||||
chr9:127461280 | C | T | 11 | a0001c0001t0001g0004a0001c0001t0001g0181a0001c0001t0001g0182others(8): Show | 12 | HG02129.hp2 NA18950.hp1 NA18955.hp1 others(9): Show |
intron_variant | MODIFIER | c.406+23C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 8/25 | chr9 | 127461280 | ||||||
chr9:127461281 | G | A | 3 | a0002c0002t0001g0067a0002c0002t0001g0072a0002c0002t0001g0138 | 3 | NA18946.hp2 NA18974.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.406+24G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 8/25 | chr9 | 127461281 | ||||||
chr9:127461473 | C | T | 1 | a0002c0002t0001g0034 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.406+216C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 8/25 | chr9 | 127461473 | ||||||
chr9:127461475 | G | A | 54 | a0001c0001t0001g0005a0001c0001t0001g0204a0001c0001t0001g0205others(51): Show | 55 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.406+218G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 8/25 | chr9 | 127461475 | ||||||
chr9:127461543 | G | A | 58 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0279others(55): Show | 60 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.406+286G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 8/25 | chr9 | 127461543 | ||||||
chr9:127461605 | A | G | 1 | a0001c0001t0001g0229 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.406+348A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 8/25 | chr9 | 127461605 | ||||||
chr9:127461649 | G | A | 11 | a0001c0001t0001g0004a0001c0001t0001g0181a0001c0001t0001g0182others(8): Show | 12 | HG02129.hp2 NA18950.hp1 NA18955.hp1 others(9): Show |
intron_variant | MODIFIER | c.406+392G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 8/25 | chr9 | 127461649 | ||||||
chr9:127461846 | A | C | 1 | a0001c0003t0001g0137 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.407-406A>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 8/25 | chr9 | 127461846 | ||||||
chr9:127462098 | T | G | 1 | a0002c0002t0001g0039 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.407-154T>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 8/25 | chr9 | 127462098 | ||||||
chr9:127462217 | T | G | 2 | a0001c0003t0001g0033a0001c0003t0001g0073 | 2 | NA19056.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.407-35T>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 8/25 | chr9 | 127462217 | ||||||
chr9:127462450 | T | C | 1 | a0002c0002t0001g0045 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.528+77T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127462450 | ||||||
chr9:127462506 | G | C | 9 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(6): Show | 9 | HG01884.hp2 HG02451.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.528+133G>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127462506 | ||||||
chr9:127462626 | A | G | 1 | a0001c0003t0001g0136 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.528+253A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127462626 | ||||||
chr9:127462648 | A | G | 180 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(177): Show | 184 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.528+275A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127462648 | ||||||
chr9:127462855 | TA | T | 6 | a0001c0001t0001g0189a0001c0001t0001g0270a0001c0001t0001g0289others(3): Show | 6 | HG01168.hp1 HG02523.hp1 NA18957.hp2 others(3): Show |
intron_variant | MODIFIER | c.528+495delA | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127462855 | |||||
chr9:127462883 | G | C | 1 | a0001c0001t0001g0277 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.528+510G>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127462883 | ||||||
chr9:127462892 | T | C | 2 | a0001c0003t0001g0173a0007c0011t0001g0174 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.528+519T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127462892 | ||||||
chr9:127462948 | C | A | 1 | a0001c0003t0001g0043 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.528+575C>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127462948 | ||||||
chr9:127462949 | A | G | 10 | a0002c0002t0001g0001a0002c0002t0001g0036a0002c0002t0001g0037others(7): Show | 11 | HG01109.hp2 HG02258.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.528+576A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127462949 | ||||||
chr9:127463148 | G | A | 2 | a0001c0001t0001g0277a0002c0002t0001g0066 | 2 | HG01496.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.528+775G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127463148 | ||||||
chr9:127463156 | G | A | 11 | a0001c0001t0001g0004a0001c0001t0001g0181a0001c0001t0001g0182others(8): Show | 12 | HG02129.hp2 NA18950.hp1 NA18955.hp1 others(9): Show |
intron_variant | MODIFIER | c.528+783G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127463156 | ||||||
chr9:127463198 | C | CA | 86 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0021others(83): Show | 89 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.528+848dupA | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127463198 | |||||
chr9:127463198 | CA | C | 93 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0012others(90): Show | 95 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.528+848delA | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127463198 | |||||
chr9:127463227 | A | G | 1 | a0001c0001t0001g0007 | 2 | HG00099.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.528+854A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127463227 | ||||||
chr9:127463233 | C | T | 2 | a0001c0001t0001g0193a0001c0001t0001g0201 | 2 | HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.528+860C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127463233 | ||||||
chr9:127463341 | A | C | 1 | a0002c0002t0001g0179 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.528+968A>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127463341 | ||||||
chr9:127463433 | G | A | 2 | a0001c0003t0001g0173a0007c0011t0001g0174 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.528+1060G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127463433 | ||||||
chr9:127463497 | G | A | 1 | a0001c0001t0001g0292 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.528+1124G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127463497 | ||||||
chr9:127464016 | C | T | 1 | a0001c0001t0001g0240 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.528+1643C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127464016 | ||||||
chr9:127464234 | G | A | 4 | a0001c0001t0001g0012a0001c0001t0001g0013a0002c0005t0001g0018others(1): Show | 4 | HG03041.hp1 HG03471.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.528+1861G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127464234 | ||||||
chr9:127464289 | A | G | 2 | a0001c0003t0001g0173a0007c0011t0001g0174 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.528+1916A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127464289 | ||||||
chr9:127464362 | TGACCGTG others(49): Show |
T | 76 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(73): Show | 78 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.528+2011_528+2066d others(58): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127464362 | |||||
chr9:127464380 | C | T | 3 | a0001c0003t0001g0130a0001c0003t0001g0173a0007c0011t0001g0174 | 3 | HG02055.hp1 HG03579.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.528+2007C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127464380 | ||||||
chr9:127464422 | C | G | 2 | a0001c0003t0001g0173a0007c0011t0001g0174 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.528+2049C>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127464422 | ||||||
chr9:127464475 | A | T | 2 | a0001c0003t0001g0173a0007c0011t0001g0174 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.528+2102A>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127464475 | ||||||
chr9:127464579 | A | G | 1 | a0002c0002t0001g0129 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.528+2206A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127464579 | ||||||
chr9:127464594 | A | C | 1 | a0002c0002t0001g0063 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.528+2221A>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127464594 | ||||||
chr9:127464630 | T | C | 180 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(177): Show | 184 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.528+2257T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127464630 | ||||||
chr9:127464800 | T | A | 104 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(101): Show | 106 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.528+2427T>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127464800 | ||||||
chr9:127465075 | G | A | 1 | a0001c0001t0001g0293 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.529-2665G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127465075 | ||||||
chr9:127465077 | C | CA | 4 | a0001c0001t0001g0277a0001c0007t0001g0275a0001c0007t0001g0276others(1): Show | 4 | HG01109.hp1 HG02630.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.529-2662dupA | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127465077 | |||||
chr9:127465083 | C | T | 1 | a0001c0001t0001g0332 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.529-2657C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127465083 | ||||||
chr9:127465275 | T | C | 2 | a0001c0003t0001g0173a0007c0011t0001g0174 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.529-2465T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127465275 | ||||||
chr9:127465374 | A | T | 1 | a0002c0002t0001g0128 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.529-2366A>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127465374 | ||||||
chr9:127465665 | G | A | 2 | a0001c0003t0001g0078a0001c0016t0001g0079 | 2 | HG03834.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.529-2075G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127465665 | ||||||
chr9:127465808 | G | T | 4 | a0001c0001t0001g0209a0001c0001t0001g0227a0001c0001t0001g0228others(1): Show | 4 | NA18957.hp1 NA18989.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.529-1932G>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127465808 | ||||||
chr9:127465996 | C | CA | 88 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0017others(85): Show | 89 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.529-1736dupA | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127465996 | |||||
chr9:127466005 | T | C | 9 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(6): Show | 9 | HG01884.hp2 HG02451.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.529-1735T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466005 | ||||||
chr9:127466165 | C | T | 180 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(177): Show | 184 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.529-1575C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466165 | ||||||
chr9:127466166 | G | A | 1 | a0001c0003t0001g0080 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.529-1574G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466166 | ||||||
chr9:127466216 | A | G | 104 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(101): Show | 106 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.529-1524A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466216 | ||||||
chr9:127466232 | T | C | 180 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(177): Show | 184 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.529-1508T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466232 | ||||||
chr9:127466290 | C | G | 180 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(177): Show | 184 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.529-1450C>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466290 | ||||||
chr9:127466474 | T | C | 1 | a0001c0001t0001g0206 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.529-1266T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466474 | ||||||
chr9:127466475 | C | CAT | 9 | a0001c0003t0001g0033a0001c0003t0001g0105a0001c0003t0001g0112others(6): Show | 9 | HG00323.hp2 HG01070.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.529-1236_529-1235d others(4): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466475 | |||||
chr9:127466475 | C | CATAT | 8 | a0001c0001t0001g0183a0001c0001t0001g0185a0001c0001t0001g0190others(5): Show | 9 | HG01255.hp1 HG02886.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.529-1238_529-1235d others(6): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466475 | |||||
chr9:127466475 | C | CATATAT | 17 | a0001c0001t0001g0004a0001c0001t0001g0181a0001c0001t0001g0186others(14): Show | 18 | HG01106.hp2 HG01884.hp2 HG02056.hp2 others(15): Show |
intron_variant | MODIFIER | c.529-1240_529-1235d others(8): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466475 | |||||
chr9:127466475 | C | CATATATA others(1): Show |
5 | a0001c0003t0001g0082a0001c0003t0001g0167a0002c0002t0001g0032others(2): Show | 5 | HG02451.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.529-1242_529-1235d others(10): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466475 | |||||
chr9:127466475 | C | CATATATA others(3): Show |
1 | a0001c0003t0001g0152 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.529-1244_529-1235d others(12): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466475 | |||||
chr9:127466475 | C | CATATATA others(7): Show |
2 | a0002c0002t0001g0061a0002c0002t0001g0169 | 2 | HG01081.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.529-1248_529-1235d others(16): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466475 | |||||
chr9:127466475 | C | CATATATA others(9): Show |
1 | a0002c0002t0001g0081 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.529-1250_529-1235d others(18): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466475 | |||||
chr9:127466475 | CAT | C | 3 | a0001c0001t0001g0202a0001c0001t0001g0206a0002c0002t0001g0123 | 3 | HG00639.hp2 NA19043.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.529-1236_529-1235d others(4): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466475 | |||||
chr9:127466475 | CATATATA others(1): Show |
C | 25 | a0001c0001t0001g0204a0001c0001t0001g0212a0001c0001t0001g0223others(22): Show | 26 | HG00621.hp1 HG00673.hp2 HG00733.hp1 others(23): Show |
intron_variant | MODIFIER | c.529-1242_529-1235d others(10): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466475 | |||||
chr9:127466475 | CATATATA others(3): Show |
C | 7 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0001t0001g0269others(4): Show | 7 | HG00423.hp1 HG00609.hp1 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.529-1244_529-1235d others(12): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466475 | |||||
chr9:127466492 | ATATATAT others(11): Show |
A | 1 | a0001c0003t0001g0159 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.529-1246_529-1229d others(20): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466492 | |||||
chr9:127466493 | TATATATA others(2): Show |
T | 5 | a0001c0001t0001g0228a0001c0001t0001g0270a0002c0002t0001g0038others(2): Show | 5 | HG01109.hp2 HG02523.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.529-1246_529-1238d others(11): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466493 | ||||||
chr9:127466494 | ATATATAT others(4): Show |
A | 3 | a0001c0001t0001g0216a0001c0001t0001g0217a0001c0001t0001g0250 | 3 | HG00642.hp2 HG00738.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.529-1244_529-1234d others(13): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466494 | |||||
chr9:127466494 | ATATATAT others(10): Show |
A | 1 | a0001c0001t0001g0209 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.529-1244_529-1228d others(19): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466494 | |||||
chr9:127466494 | ATATATAT others(11): Show |
A | 1 | a0002c0005t0001g0215 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.529-1244_529-1227d others(20): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466494 | |||||
chr9:127466495 | TATATATA | T | 4 | a0001c0001t0001g0203a0001c0001t0001g0205a0001c0001t0001g0229others(1): Show | 4 | HG00735.hp2 HG01358.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.529-1244_529-1238d others(9): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466495 | ||||||
chr9:127466495 | TATATATA others(2): Show |
T | 12 | a0001c0001t0001g0005a0001c0001t0001g0220a0001c0001t0001g0221others(9): Show | 13 | HG00099.hp2 HG00323.hp1 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.529-1244_529-1236d others(11): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466495 | ||||||
chr9:127466496 | ATATATAT others(5): Show |
A | 1 | a0001c0001t0001g0256 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.529-1242_529-1231d others(14): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466496 | |||||
chr9:127466496 | ATATATAT others(13): Show |
A | 1 | a0001c0001t0001g0211 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.529-1242_529-1223d others(22): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466496 | |||||
chr9:127466497 | TATATATA | T | 7 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0235others(4): Show | 7 | HG01261.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.529-1242_529-1236d others(9): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466497 | ||||||
chr9:127466498 | ATATATAT others(5): Show |
A | 2 | a0001c0001t0001g0023a0001c0001t0001g0255 | 2 | HG02717.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.529-1240_529-1229d others(14): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466498 | |||||
chr9:127466498 | ATATATAT others(6): Show |
A | 1 | a0001c0001t0001g0022 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.529-1240_529-1228d others(15): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466498 | |||||
chr9:127466500 | A | T | 2 | a0002c0002t0001g0001a0002c0002t0001g0150 | 3 | HG03471.hp1 HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.529-1240A>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466500 | ||||||
chr9:127466500 | ATATATTT others(4): Show |
A | 1 | a0001c0001t0001g0021 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.529-1238_529-1228d others(13): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466500 | |||||
chr9:127466502 | A | ATT | 3 | a0002c0002t0001g0149a0002c0002t0001g0162a0002c0002t0003g0171 | 3 | NA18955.hp2 NA19066.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.529-1237_529-1236i others(4): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466502 | |||||
chr9:127466502 | A | T | 14 | a0001c0001t0001g0226a0001c0001t0001g0239a0001c0001t0001g0247others(11): Show | 15 | HG01952.hp1 HG01981.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.529-1238A>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466502 | ||||||
chr9:127466504 | A | ATATATAT others(6): Show |
1 | a0001c0003t0001g0078 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.529-1235_529-1234i others(15): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466504 | |||||
chr9:127466504 | A | ATATATAT others(8): Show |
2 | a0002c0002t0001g0170a0002c0002t0001g0177 | 2 | HG00280.hp1 HG00280.hp2 |
intron_variant | MODIFIER | c.529-1235_529-1234i others(17): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466504 | |||||
chr9:127466504 | A | ATATATAT others(10): Show |
1 | a0001c0001t0002g0027 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.529-1235_529-1234i others(19): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466504 | |||||
chr9:127466504 | A | ATATATAT others(16): Show |
1 | a0002c0002t0005g0046 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.529-1235_529-1234i others(25): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466504 | |||||
chr9:127466504 | A | ATATATAT others(13): Show |
1 | a0002c0002t0001g0045 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.529-1235_529-1234i others(22): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466504 | |||||
chr9:127466504 | A | ATATATAT others(13): Show |
2 | a0001c0003t0001g0083a0001c0003t0001g0084 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.529-1235_529-1234i others(22): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466504 | |||||
chr9:127466504 | A | ATATATAT others(9): Show |
1 | a0002c0002t0001g0048 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.529-1235_529-1234i others(18): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466504 | |||||
chr9:127466504 | A | ATATATAT others(10): Show |
1 | a0002c0002t0001g0062 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.529-1235_529-1234i others(19): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466504 | |||||
chr9:127466504 | A | ATATATAT others(8): Show |
3 | a0002c0002t0001g0049a0002c0002t0001g0056a0002c0005t0002g0028 | 3 | HG01169.hp2 HG01258.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.529-1235_529-1234i others(17): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466504 | |||||
chr9:127466504 | A | ATATATAT others(10): Show |
2 | a0002c0002t0001g0050a0002c0002t0001g0059 | 2 | HG03834.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.529-1235_529-1234i others(19): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466504 | |||||
chr9:127466504 | A | ATATATAT others(5): Show |
2 | a0002c0002t0001g0057a0002c0002t0001g0178 | 2 | HG01358.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.529-1235_529-1234i others(14): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466504 | |||||
chr9:127466504 | A | ATATATAT others(6): Show |
1 | a0002c0002t0001g0051 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.529-1235_529-1234i others(15): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466504 | |||||
chr9:127466504 | A | ATATATAT others(3): Show |
1 | a0002c0002t0001g0042 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.529-1235_529-1234i others(12): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466504 | |||||
chr9:127466504 | A | ATATATAT others(4): Show |
3 | a0002c0002t0001g0035a0002c0002t0001g0052a0002c0002t0001g0065 | 3 | HG01952.hp2 HG03098.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.529-1235_529-1234i others(13): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466504 | |||||
chr9:127466504 | A | ATATATAT others(5): Show |
4 | a0002c0002t0001g0053a0002c0002t0001g0055a0002c0002t0001g0179others(1): Show | 4 | HG00738.hp2 HG01106.hp1 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.529-1235_529-1234i others(14): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466504 | |||||
chr9:127466504 | A | ATATATAT others(6): Show |
3 | a0001c0003t0001g0074a0001c0003t0001g0088a0002c0002t0001g0063 | 3 | HG00140.hp2 HG01192.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.529-1235_529-1234i others(15): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466504 | |||||
chr9:127466504 | A | ATATATAT others(5): Show |
3 | a0001c0003t0001g0096a0001c0003t0001g0097a0001c0003t0001g0098 | 3 | HG00741.hp2 HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.529-1235_529-1234i others(14): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466504 | |||||
chr9:127466504 | A | ATATATTT others(7): Show |
1 | a0002c0002t0001g0060 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.529-1235_529-1234i others(16): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466504 | |||||
chr9:127466504 | A | ATATTTTT others(8): Show |
1 | a0002c0002t0001g0058 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.529-1235_529-1234i others(17): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466504 | |||||
chr9:127466504 | A | ATT | 7 | a0001c0003t0001g0011a0001c0003t0001g0120a0001c0003t0001g0176others(4): Show | 7 | HG00438.hp2 HG02083.hp2 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.529-1211_529-1210d others(4): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466504 | |||||
chr9:127466504 | A | T | 49 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205others(46): Show | 50 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.529-1236A>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466504 | ||||||
chr9:127466504 | AT | A | 6 | a0001c0003t0001g0100a0001c0003t0001g0113a0001c0003t0001g0144others(3): Show | 6 | HG02004.hp2 HG02257.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.529-1210delT | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466504 | |||||
chr9:127466505 | T | TA | 27 | a0001c0001t0001g0279a0001c0001t0001g0282a0001c0001t0001g0284others(24): Show | 27 | HG00621.hp2 HG00639.hp1 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.529-1235_529-1234i others(3): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466505 | ||||||
chr9:127466505 | T | TATA | 21 | a0001c0001t0001g0184a0001c0001t0001g0201a0001c0001t0001g0280others(18): Show | 21 | HG00558.hp1 HG01255.hp2 HG01261.hp1 others(18): Show |
intron_variant | MODIFIER | c.529-1235_529-1234i others(5): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466505 | ||||||
chr9:127466505 | T | TATATA | 13 | a0001c0001t0001g0291a0001c0001t0001g0294a0001c0001t0001g0295others(10): Show | 13 | HG00558.hp2 HG00642.hp1 HG01993.hp2 others(10): Show |
intron_variant | MODIFIER | c.529-1235_529-1234i others(7): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466505 | ||||||
chr9:127466505 | T | TATATATA | 8 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0298others(5): Show | 10 | HG00099.hp1 HG01361.hp2 HG03669.hp2 others(7): Show |
intron_variant | MODIFIER | c.529-1235_529-1234i others(9): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466505 | ||||||
chr9:127466505 | T | TATATATA others(6): Show |
2 | a0001c0001t0001g0309a0001c0001t0001g0330 | 2 | HG01981.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.529-1235_529-1234i others(15): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466505 | ||||||
chr9:127466505 | T | TATATATA others(10): Show |
1 | a0002c0002t0001g0047 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.529-1235_529-1234i others(19): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466505 | ||||||
chr9:127466506 | T | A | 67 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0014others(64): Show | 69 | HG00323.hp2 HG00438.hp1 HG01070.hp2 others(66): Show |
intron_variant | MODIFIER | c.529-1234T>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466506 | ||||||
chr9:127466507 | T | A | 62 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0184others(59): Show | 64 | HG00099.hp1 HG00558.hp2 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.529-1233T>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466507 | ||||||
chr9:127466508 | T | A | 53 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0181others(50): Show | 55 | HG00438.hp1 HG01106.hp2 HG01109.hp1 others(52): Show |
intron_variant | MODIFIER | c.529-1232T>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466508 | ||||||
chr9:127466509 | T | A | 44 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0184others(41): Show | 46 | HG00099.hp1 HG00558.hp2 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.529-1231T>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466509 | ||||||
chr9:127466510 | T | A | 50 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0181others(47): Show | 52 | HG00438.hp1 HG01106.hp2 HG01109.hp1 others(49): Show |
intron_variant | MODIFIER | c.529-1230T>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466510 | ||||||
chr9:127466511 | T | A | 38 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0184others(35): Show | 40 | HG00099.hp1 HG00558.hp2 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.529-1229T>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466511 | ||||||
chr9:127466511 | T | TAC | 3 | a0001c0007t0001g0275a0001c0007t0001g0276a0001c0007t0001g0278 | 3 | HG01109.hp1 HG02723.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.529-1229_529-1228i others(4): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466511 | ||||||
chr9:127466512 | T | A | 42 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0181others(39): Show | 43 | HG00438.hp1 HG01081.hp1 HG01106.hp2 others(40): Show |
intron_variant | MODIFIER | c.529-1228T>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466512 | ||||||
chr9:127466513 | T | A | 37 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0184others(34): Show | 39 | HG00099.hp1 HG00558.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.529-1227T>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466513 | ||||||
chr9:127466514 | T | A | 25 | a0001c0001t0001g0004a0001c0001t0001g0181a0001c0001t0001g0182others(22): Show | 26 | HG00438.hp1 HG01106.hp2 HG01943.hp1 others(23): Show |
intron_variant | MODIFIER | c.529-1226T>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466514 | ||||||
chr9:127466515 | T | A | 34 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0279others(31): Show | 36 | HG00099.hp1 HG00558.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.529-1225T>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466515 | ||||||
chr9:127466516 | T | A | 16 | a0001c0001t0001g0004a0001c0001t0001g0181a0001c0001t0001g0182others(13): Show | 18 | HG00438.hp1 HG01106.hp2 HG01943.hp2 others(15): Show |
intron_variant | MODIFIER | c.529-1224T>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466516 | ||||||
chr9:127466516 | TTTTTTTT others(8): Show |
T | 1 | a0001c0001t0001g0313 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.529-1223_529-1209d others(17): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466516 | ||||||
chr9:127466517 | T | A | 18 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0284others(15): Show | 18 | HG00558.hp2 HG00639.hp1 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.529-1223T>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466517 | ||||||
chr9:127466518 | T | A | 4 | a0001c0001t0001g0182a0001c0001t0001g0299a0001c0001t0001g0308others(1): Show | 4 | HG01106.hp2 HG02129.hp2 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.529-1222T>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466518 | ||||||
chr9:127466519 | T | A | 9 | a0001c0001t0001g0280a0001c0001t0001g0284a0001c0001t0001g0291others(6): Show | 9 | HG00558.hp2 HG02155.hp1 NA18943.hp2 others(6): Show |
intron_variant | MODIFIER | c.529-1221T>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466519 | ||||||
chr9:127466520 | T | A | 3 | a0001c0001t0001g0182a0001c0001t0001g0299a0001c0001t0001g0308 | 3 | HG02129.hp2 NA18999.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.529-1220T>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466520 | ||||||
chr9:127466521 | T | A | 1 | a0001c0001t0001g0284 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.529-1219T>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466521 | ||||||
chr9:127466522 | T | A | 1 | a0001c0001t0001g0308 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.529-1218T>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466522 | ||||||
chr9:127466530 | T | C | 1 | a0007c0011t0001g0174 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.529-1210T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466530 | ||||||
chr9:127466530 | TC | T | 13 | a0001c0001t0001g0182a0001c0001t0001g0283a0001c0001t0001g0285others(10): Show | 13 | HG00438.hp1 HG01943.hp1 HG01943.hp2 others(10): Show |
intron_variant | MODIFIER | c.529-1208delC | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 127466530 | |||||
chr9:127466531 | C | T | 154 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(151): Show | 158 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.529-1209C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466531 | ||||||
chr9:127466567 | G | A | 4 | a0001c0001t0001g0209a0001c0001t0001g0227a0001c0001t0001g0228others(1): Show | 4 | NA18957.hp1 NA18989.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.529-1173G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466567 | ||||||
chr9:127466707 | T | C | 3 | a0001c0007t0001g0275a0001c0007t0001g0276a0001c0007t0001g0278 | 3 | HG01109.hp1 HG02723.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.529-1033T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466707 | ||||||
chr9:127466862 | G | T | 4 | a0001c0001t0001g0267a0001c0001t0001g0268a0001c0001t0001g0269others(1): Show | 4 | HG00609.hp1 HG00621.hp1 HG02165.hp1 others(1): Show |
intron_variant | MODIFIER | c.529-878G>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466862 | ||||||
chr9:127466876 | G | T | 1 | a0001c0001t0001g0021 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.529-864G>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466876 | ||||||
chr9:127466886 | C | T | 2 | a0002c0002t0001g0119a0002c0002t0001g0123 | 2 | NA18948.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.529-854C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466886 | ||||||
chr9:127466951 | C | T | 1 | a0002c0002t0001g0032 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.529-789C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466951 | ||||||
chr9:127466975 | C | T | 1 | a0007c0011t0001g0174 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.529-765C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466975 | ||||||
chr9:127466983 | A | G | 104 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(101): Show | 106 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.529-757A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127466983 | ||||||
chr9:127467058 | C | T | 1 | a0002c0002t0001g0034 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.529-682C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127467058 | ||||||
chr9:127467127 | T | C | 17 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0021others(14): Show | 17 | HG01884.hp2 HG02055.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.529-613T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127467127 | ||||||
chr9:127467128 | T | C | 1 | a0001c0001t0001g0014 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.529-612T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127467128 | ||||||
chr9:127467130 | G | T | 1 | a0001c0001t0001g0225 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.529-610G>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127467130 | ||||||
chr9:127467285 | C | A | 98 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(95): Show | 100 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.529-455C>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127467285 | ||||||
chr9:127467373 | A | G | 182 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(179): Show | 186 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.529-367A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127467373 | ||||||
chr9:127467374 | C | T | 1 | a0003c0004t0001g0015 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.529-366C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127467374 | ||||||
chr9:127467494 | C | T | 3 | a0001c0007t0001g0275a0001c0007t0001g0276a0001c0007t0001g0278 | 3 | HG01109.hp1 HG02723.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.529-246C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127467494 | ||||||
chr9:127467718 | C | T | 1 | a0002c0002t0001g0128 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.529-22C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 9/25 | chr9 | 127467718 | ||||||
chr9:127467843 | C | T | 2 | a0001c0001t0001g0287a0001c0001t0001g0290 | 2 | NA18979.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.619+13C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127467843 | ||||||
chr9:127468030 | C | T | 3 | a0002c0002t0001g0119a0002c0002t0001g0123a0002c0002t0001g0175 | 3 | NA18948.hp1 NA19064.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.619+200C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127468030 | ||||||
chr9:127468235 | A | G | 184 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(181): Show | 188 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.619+405A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127468235 | ||||||
chr9:127468367 | G | A | 5 | a0002c0002t0001g0106a0002c0002t0001g0109a0002c0002t0001g0133others(2): Show | 5 | HG01168.hp1 HG01169.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.619+537G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127468367 | ||||||
chr9:127468432 | G | A | 12 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(9): Show | 12 | HG02486.hp2 HG02717.hp2 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.619+602G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127468432 | ||||||
chr9:127468810 | C | CA | 56 | a0001c0001t0001g0013a0001c0001t0001g0240a0001c0001t0001g0252others(53): Show | 57 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.619+1009dupA | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr9 | 127468810 | |||||
chr9:127468810 | C | CAAA | 6 | a0001c0001t0001g0004a0001c0001t0001g0183a0001c0001t0001g0185others(3): Show | 7 | HG03942.hp2 NA18959.hp2 NA18966.hp2 others(4): Show |
intron_variant | MODIFIER | c.619+1007_619+1009d others(5): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr9 | 127468810 | |||||
chr9:127468810 | CAAAAAAA others(2): Show |
C | 6 | a0001c0001t0001g0277a0001c0007t0001g0275a0001c0007t0001g0276others(3): Show | 6 | HG00733.hp2 HG01109.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.619+1001_619+1009d others(11): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr9 | 127468810 | |||||
chr9:127468810 | CAAAAAAA others(8): Show |
C | 5 | a0001c0001t0001g0284a0001c0001t0001g0291a0001c0001t0001g0296others(2): Show | 5 | NA18943.hp2 NA18948.hp2 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.619+995_619+1009de others(16): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr9 | 127468810 | |||||
chr9:127468834 | A | AAC | 19 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0209others(16): Show | 19 | HG00621.hp1 HG00738.hp1 HG01433.hp1 others(16): Show |
intron_variant | MODIFIER | c.619+1005_619+1006i others(4): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr9 | 127468834 | |||||
chr9:127468834 | A | AC | 64 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0017others(61): Show | 65 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.619+1004_619+1005i others(3): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127468834 | ||||||
chr9:127468834 | A | C | 2 | a0001c0001t0001g0203a0001c0001t0001g0247 | 2 | HG00735.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.619+1004A>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127468834 | ||||||
chr9:127469138 | A | G | 180 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(177): Show | 184 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.619+1308A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127469138 | ||||||
chr9:127469326 | T | C | 1 | a0001c0001t0001g0294 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.619+1496T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127469326 | ||||||
chr9:127469356 | G | C | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.619+1526G>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127469356 | ||||||
chr9:127469435 | A | G | 325 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(322): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.619+1605A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127469435 | ||||||
chr9:127469593 | C | T | 11 | a0001c0001t0001g0014a0001c0003t0001g0074a0001c0003t0001g0082others(8): Show | 11 | HG00140.hp2 HG00741.hp2 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.619+1763C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127469593 | ||||||
chr9:127469620 | G | GA | 190 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(187): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.619+1801dupA | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr9 | 127469620 | |||||
chr9:127469688 | G | A | 1 | a0002c0002t0001g0128 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.619+1858G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127469688 | ||||||
chr9:127469790 | T | C | 2 | a0001c0001t0002g0027a0002c0005t0002g0028 | 2 | HG03516.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.619+1960T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127469790 | ||||||
chr9:127469836 | G | A | 1 | a0002c0002t0001g0070 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.619+2006G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127469836 | ||||||
chr9:127469878 | T | C | 1 | a0002c0002t0001g0114 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.619+2048T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127469878 | ||||||
chr9:127469889 | C | T | 1 | a0002c0002t0001g0122 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.619+2059C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127469889 | ||||||
chr9:127469913 | C | T | 1 | a0001c0001t0001g0243 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.619+2083C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127469913 | ||||||
chr9:127469920 | GCGCCACT others(1815): Show |
G | 1 | a0001c0001t0001g0243 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.619+2113_620-2037d others(2): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr9 | 127469920 | |||||
chr9:127469943 | A | C | 1 | a0001c0001t0001g0293 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.619+2113A>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127469943 | ||||||
chr9:127469944 | T | G | 1 | a0001c0001t0001g0293 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.619+2114T>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127469944 | ||||||
chr9:127470144 | T | C | 16 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0021others(13): Show | 16 | HG01884.hp2 HG02055.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.619+2314T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127470144 | ||||||
chr9:127470182 | G | A | 5 | a0001c0001t0001g0285a0001c0001t0001g0287a0001c0001t0001g0288others(2): Show | 5 | NA18959.hp1 NA18979.hp1 NA19057.hp2 others(2): Show |
intron_variant | MODIFIER | c.619+2352G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127470182 | ||||||
chr9:127470459 | A | G | 67 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(64): Show | 70 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.619+2629A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127470459 | ||||||
chr9:127470488 | G | A | 2 | a0001c0003t0001g0173a0007c0011t0001g0174 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.619+2658G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127470488 | ||||||
chr9:127470611 | T | A | 73 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0017others(70): Show | 74 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.619+2781T>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127470611 | ||||||
chr9:127470630 | G | C | 73 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0017others(70): Show | 74 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.619+2800G>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127470630 | ||||||
chr9:127470676 | G | A | 1 | a0002c0002t0001g0061 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.619+2846G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127470676 | ||||||
chr9:127470769 | T | C | 1 | a0007c0011t0001g0174 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.619+2939T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127470769 | ||||||
chr9:127470770 | G | C | 1 | a0001c0001t0001g0204 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.619+2940G>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127470770 | ||||||
chr9:127470837 | T | C | 1 | a0001c0003t0001g0099 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.620-2964T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127470837 | ||||||
chr9:127470963 | C | G | 16 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0021others(13): Show | 16 | HG01884.hp2 HG02055.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.620-2838C>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127470963 | ||||||
chr9:127471019 | C | T | 54 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0277others(51): Show | 56 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.620-2782C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127471019 | ||||||
chr9:127471111 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.620-2690C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127471111 | ||||||
chr9:127471472 | T | TA | 38 | a0001c0001t0001g0007a0001c0001t0001g0280a0001c0001t0001g0281others(35): Show | 39 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(36): Show |
intron_variant | MODIFIER | c.620-2304dupA | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr9 | 127471472 | |||||
chr9:127471472 | TA | T | 36 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0021others(33): Show | 36 | HG00438.hp1 HG00558.hp2 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.620-2304delA | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr9 | 127471472 | |||||
chr9:127471472 | TAA | T | 73 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0017others(70): Show | 74 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.620-2305_620-2304d others(4): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr9 | 127471472 | |||||
chr9:127471472 | TAAA | T | 31 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0182others(28): Show | 32 | HG01099.hp2 HG01109.hp1 HG01515.hp2 others(29): Show |
intron_variant | MODIFIER | c.620-2306_620-2304d others(5): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr9 | 127471472 | |||||
chr9:127471514 | C | T | 16 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0021others(13): Show | 16 | HG01884.hp2 HG02055.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.620-2287C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127471514 | ||||||
chr9:127471550 | G | A | 11 | a0001c0001t0001g0004a0001c0001t0001g0181a0001c0001t0001g0182others(8): Show | 12 | HG02129.hp2 NA18950.hp1 NA18955.hp1 others(9): Show |
intron_variant | MODIFIER | c.620-2251G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127471550 | ||||||
chr9:127471677 | C | T | 85 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0017others(82): Show | 86 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.620-2124C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127471677 | ||||||
chr9:127471714 | G | T | 57 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0279others(54): Show | 59 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.620-2087G>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127471714 | ||||||
chr9:127471875 | G | C | 182 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(179): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.620-1926G>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127471875 | ||||||
chr9:127471954 | C | T | 1 | a0001c0001t0001g0012 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.620-1847C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127471954 | ||||||
chr9:127472000 | C | T | 11 | a0001c0001t0001g0004a0001c0001t0001g0181a0001c0001t0001g0182others(8): Show | 12 | HG02129.hp2 NA18950.hp1 NA18955.hp1 others(9): Show |
intron_variant | MODIFIER | c.620-1801C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127472000 | ||||||
chr9:127472096 | G | T | 1 | a0002c0002t0001g0060 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.620-1705G>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127472096 | ||||||
chr9:127472119 | G | A | 2 | a0001c0003t0001g0173a0007c0011t0001g0174 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.620-1682G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127472119 | ||||||
chr9:127472252 | G | A | 16 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0021others(13): Show | 16 | HG01884.hp2 HG02055.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.620-1549G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127472252 | ||||||
chr9:127472297 | G | GTA | 11 | a0001c0001t0001g0004a0001c0001t0001g0181a0001c0001t0001g0182others(8): Show | 12 | HG02129.hp2 NA18950.hp1 NA18955.hp1 others(9): Show |
intron_variant | MODIFIER | c.620-1488_620-1487d others(4): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr9 | 127472297 | |||||
chr9:127472297 | GTA | G | 32 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(29): Show | 32 | HG00140.hp2 HG00741.hp2 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.620-1488_620-1487d others(4): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr9 | 127472297 | |||||
chr9:127472313 | A | G | 1 | a0001c0001t0001g0308 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.620-1488A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127472313 | ||||||
chr9:127472313 | ATG | A | 85 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0017others(82): Show | 86 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.620-1480_620-1479d others(4): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr9 | 127472313 | |||||
chr9:127472315 | G | A | 12 | a0001c0001t0001g0004a0001c0001t0001g0181a0001c0001t0001g0182others(9): Show | 13 | HG02129.hp2 HG03654.hp1 NA18950.hp1 others(10): Show |
intron_variant | MODIFIER | c.620-1486G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127472315 | ||||||
chr9:127472317 | G | A | 97 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(94): Show | 99 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.620-1484G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127472317 | ||||||
chr9:127472355 | A | G | 97 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(94): Show | 99 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.620-1446A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127472355 | ||||||
chr9:127472368 | A | G | 187 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(184): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.620-1433A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127472368 | ||||||
chr9:127472442 | G | A | 1 | a0002c0002t0001g0081 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.620-1359G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127472442 | ||||||
chr9:127472632 | C | G | 6 | a0002c0002t0001g0035a0002c0002t0001g0058a0002c0002t0001g0059others(3): Show | 6 | HG02145.hp1 HG02486.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.620-1169C>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127472632 | ||||||
chr9:127472759 | C | T | 2 | a0003c0004t0002g0025a0003c0004t0002g0026 | 2 | HG02055.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.620-1042C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127472759 | ||||||
chr9:127472774 | G | A | 85 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(82): Show | 87 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.620-1027G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127472774 | ||||||
chr9:127472794 | C | T | 2 | a0002c0002t0001g0133a0002c0002t0001g0158 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.620-1007C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127472794 | ||||||
chr9:127472924 | G | A | 1 | a0001c0001t0001g0191 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.620-877G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127472924 | ||||||
chr9:127473006 | AC | A | 6 | a0002c0002t0001g0003a0002c0002t0001g0066a0002c0002t0001g0075others(3): Show | 7 | HG01496.hp1 HG02280.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.620-793delC | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr9 | 127473006 | |||||
chr9:127473173 | T | C | 58 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0277others(55): Show | 60 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.620-628T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127473173 | ||||||
chr9:127473505 | C | T | 10 | a0001c0003t0001g0074a0001c0003t0001g0082a0001c0003t0001g0083others(7): Show | 10 | HG00140.hp2 HG00741.hp2 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.620-296C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127473505 | ||||||
chr9:127473522 | A | T | 1 | a0001c0003t0001g0096 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.620-279A>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127473522 | ||||||
chr9:127473581 | C | T | 11 | a0001c0001t0001g0004a0001c0001t0001g0181a0001c0001t0001g0182others(8): Show | 12 | HG02129.hp2 NA18950.hp1 NA18955.hp1 others(9): Show |
intron_variant | MODIFIER | c.620-220C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127473581 | ||||||
chr9:127473618 | G | A | 58 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0277others(55): Show | 60 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.620-183G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 10/25 | chr9 | 127473618 | ||||||
chr9:127473964 | G | A | 97 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(94): Show | 99 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.750+33G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127473964 | ||||||
chr9:127474244 | G | A | 4 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(1): Show | 4 | HG02886.hp1 HG03041.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.750+313G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127474244 | ||||||
chr9:127474260 | CT | C | 96 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(93): Show | 98 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.750+345delT | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr9 | 127474260 | |||||
chr9:127474310 | C | G | 99 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(96): Show | 101 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.750+379C>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127474310 | ||||||
chr9:127474329 | G | A | 8 | a0001c0001t0001g0006a0001c0001t0001g0298a0001c0001t0001g0304others(5): Show | 9 | NA18942.hp1 NA18962.hp1 NA18966.hp1 others(6): Show |
intron_variant | MODIFIER | c.750+398G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127474329 | ||||||
chr9:127474382 | C | T | 1 | a0001c0003t0001g0118 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.750+451C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127474382 | ||||||
chr9:127474603 | T | G | 1 | a0002c0005t0001g0018 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.750+672T>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127474603 | ||||||
chr9:127474661 | C | T | 1 | a0001c0001t0001g0245 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.750+730C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127474661 | ||||||
chr9:127474704 | C | T | 1 | a0001c0001t0001g0294 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.750+773C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127474704 | ||||||
chr9:127474709 | C | T | 1 | a0001c0001t0001g0257 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.750+778C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127474709 | ||||||
chr9:127474771 | C | T | 2 | a0001c0001t0001g0226a0001c0001t0001g0229 | 2 | HG03239.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.750+840C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127474771 | ||||||
chr9:127474789 | G | A | 10 | a0001c0003t0001g0074a0001c0003t0001g0082a0001c0003t0001g0083others(7): Show | 10 | HG00140.hp2 HG00741.hp2 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.750+858G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127474789 | ||||||
chr9:127474809 | C | T | 1 | a0001c0003t0001g0132 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.750+878C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127474809 | ||||||
chr9:127474967 | T | A | 3 | a0001c0001t0001g0205a0001c0001t0001g0238a0001c0001t0001g0248 | 3 | HG01978.hp1 HG02738.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.750+1036T>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127474967 | ||||||
chr9:127475047 | T | TTTA | 103 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0021others(100): Show | 105 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.750+1140_750+1142d others(5): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr9 | 127475047 | |||||
chr9:127475047 | T | TTTATTA | 4 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0188others(1): Show | 4 | HG02258.hp2 HG02738.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.750+1137_750+1142d others(8): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr9 | 127475047 | |||||
chr9:127475077 | T | C | 99 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(96): Show | 101 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.750+1146T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127475077 | ||||||
chr9:127475319 | T | G | 9 | a0002c0002t0001g0039a0002c0002t0001g0085a0002c0002t0001g0089others(6): Show | 9 | HG00621.hp2 HG02165.hp2 NA18956.hp1 others(6): Show |
intron_variant | MODIFIER | c.750+1388T>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127475319 | ||||||
chr9:127475342 | T | G | 16 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0021others(13): Show | 16 | HG01884.hp2 HG02055.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.750+1411T>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127475342 | ||||||
chr9:127475413 | T | G | 1 | a0002c0002t0001g0114 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.750+1482T>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127475413 | ||||||
chr9:127475448 | G | A | 1 | a0001c0001t0002g0027 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.750+1517G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127475448 | ||||||
chr9:127475493 | TCAAA | T | 87 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(84): Show | 89 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.750+1581_750+1584d others(6): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr9 | 127475493 | |||||
chr9:127475745 | T | A | 188 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(185): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.750+1814T>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127475745 | ||||||
chr9:127475749 | A | AT | 6 | a0002c0002t0001g0035a0002c0002t0001g0058a0002c0002t0001g0059others(3): Show | 6 | HG02145.hp1 HG02486.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.750+1827dupT | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr9 | 127475749 | |||||
chr9:127475749 | A | T | 1 | a0001c0001t0001g0282 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.750+1818A>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127475749 | ||||||
chr9:127475833 | C | T | 1 | a0001c0001t0001g0328 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.750+1902C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127475833 | ||||||
chr9:127475834 | G | A | 1 | a0001c0003t0001g0086 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.750+1903G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127475834 | ||||||
chr9:127475843 | T | C | 99 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(96): Show | 101 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.750+1912T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127475843 | ||||||
chr9:127475881 | C | T | 99 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(96): Show | 101 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.750+1950C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127475881 | ||||||
chr9:127475902 | G | A | 1 | a0001c0001t0001g0313 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.750+1971G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127475902 | ||||||
chr9:127475912 | G | A | 42 | a0001c0001t0001g0306a0001c0001t0001g0312a0001c0003t0001g0010others(39): Show | 42 | HG00323.hp2 HG00558.hp1 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.750+1981G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127475912 | ||||||
chr9:127476015 | C | T | 4 | a0001c0001t0001g0332a0004c0006t0001g0331a0004c0006t0001g0333others(1): Show | 4 | HG02129.hp1 NA18974.hp2 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.750+2084C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127476015 | ||||||
chr9:127476189 | A | C | 1 | a0002c0005t0001g0018 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.750+2258A>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127476189 | ||||||
chr9:127476248 | G | A | 1 | a0001c0001t0001g0328 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.750+2317G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127476248 | ||||||
chr9:127476261 | A | G | 187 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(184): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.750+2330A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127476261 | ||||||
chr9:127476297 | A | G | 3 | a0001c0007t0001g0275a0001c0007t0001g0276a0001c0007t0001g0278 | 3 | HG01109.hp1 HG02723.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.750+2366A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127476297 | ||||||
chr9:127476366 | C | G | 86 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0017others(83): Show | 87 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.750+2435C>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127476366 | ||||||
chr9:127476425 | G | A | 85 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(82): Show | 87 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.750+2494G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127476425 | ||||||
chr9:127476550 | A | G | 3 | a0001c0001t0001g0012a0001c0001t0001g0013a0003c0004t0001g0015 | 3 | HG03041.hp1 HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.751-2384A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127476550 | ||||||
chr9:127476651 | G | A | 1 | a0002c0005t0001g0018 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.751-2283G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127476651 | ||||||
chr9:127476680 | T | C | 16 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0021others(13): Show | 16 | HG01884.hp2 HG02055.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.751-2254T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127476680 | ||||||
chr9:127476809 | G | T | 1 | a0001c0001t0001g0016 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.751-2125G>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127476809 | ||||||
chr9:127476955 | G | A | 1 | a0002c0005t0001g0018 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.751-1979G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127476955 | ||||||
chr9:127477052 | A | G | 1 | a0001c0001t0001g0198 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.751-1882A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127477052 | ||||||
chr9:127477054 | T | C | 1 | a0001c0001t0001g0182 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.751-1880T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127477054 | ||||||
chr9:127477063 | G | A | 58 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0277others(55): Show | 60 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.751-1871G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127477063 | ||||||
chr9:127477087 | C | T | 2 | a0001c0003t0001g0173a0007c0011t0001g0174 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.751-1847C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127477087 | ||||||
chr9:127477224 | G | T | 2 | a0001c0003t0001g0173a0007c0011t0001g0174 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.751-1710G>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127477224 | ||||||
chr9:127477408 | A | G | 1 | a0003c0004t0001g0015 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.751-1526A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127477408 | ||||||
chr9:127477515 | C | T | 1 | a0002c0005t0001g0018 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.751-1419C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127477515 | ||||||
chr9:127477621 | G | A | 97 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(94): Show | 99 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.751-1313G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127477621 | ||||||
chr9:127477692 | G | A | 1 | a0001c0001t0001g0207 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.751-1242G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127477692 | ||||||
chr9:127477697 | C | T | 3 | a0001c0007t0001g0275a0001c0007t0001g0276a0001c0007t0001g0278 | 3 | HG01109.hp1 HG02723.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.751-1237C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127477697 | ||||||
chr9:127477755 | A | C | 3 | a0001c0001t0001g0012a0001c0001t0001g0013a0003c0004t0001g0015 | 3 | HG03041.hp1 HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.751-1179A>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127477755 | ||||||
chr9:127477770 | G | A | 16 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0021others(13): Show | 16 | HG01884.hp2 HG02055.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.751-1164G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127477770 | ||||||
chr9:127477774 | G | A | 1 | a0002c0002t0001g0166 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.751-1160G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127477774 | ||||||
chr9:127477906 | G | A | 13 | a0001c0003t0001g0074a0001c0003t0001g0082a0001c0003t0001g0083others(10): Show | 13 | HG00140.hp2 HG00741.hp2 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.751-1028G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127477906 | ||||||
chr9:127478040 | A | G | 229 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(226): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.751-894A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127478040 | ||||||
chr9:127478052 | C | CA | 15 | a0001c0001t0001g0198a0001c0001t0001g0209a0001c0001t0001g0220others(12): Show | 15 | HG01192.hp2 HG01433.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.751-864dupA | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr9 | 127478052 | |||||
chr9:127478052 | CA | C | 21 | a0001c0001t0001g0004a0001c0001t0001g0181a0001c0001t0001g0182others(18): Show | 22 | HG00639.hp2 HG00741.hp2 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.751-864delA | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr9 | 127478052 | |||||
chr9:127478460 | G | A | 2 | a0001c0001t0001g0194a0001c0001t0001g0195 | 2 | HG02717.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.751-474G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127478460 | ||||||
chr9:127478479 | T | C | 1 | a0002c0002t0001g0032 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.751-455T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127478479 | ||||||
chr9:127478500 | T | C | 1 | a0002c0002t0001g0038 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.751-434T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127478500 | ||||||
chr9:127478502 | G | T | 10 | a0001c0001t0001g0004a0001c0001t0001g0181a0001c0001t0001g0183others(7): Show | 11 | NA18950.hp1 NA18955.hp1 NA18959.hp2 others(8): Show |
intron_variant | MODIFIER | c.751-432G>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127478502 | ||||||
chr9:127478624 | A | G | 1 | a0001c0001t0001g0187 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.751-310A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127478624 | ||||||
chr9:127478687 | A | C | 16 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0021others(13): Show | 16 | HG01884.hp2 HG02055.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.751-247A>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127478687 | ||||||
chr9:127478701 | A | G | 230 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(227): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.751-233A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 11/25 | chr9 | 127478701 | ||||||
chr9:127479043 | G | T | 10 | a0002c0002t0001g0001a0002c0002t0001g0036a0002c0002t0001g0037others(7): Show | 11 | HG01109.hp2 HG02258.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.780+80G>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 12/25 | chr9 | 127479043 | ||||||
chr9:127479095 | G | GCA | 230 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(227): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.780+133_780+134dup others(2): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 12/25 | INFO_REALIGN_3_PRIME | chr9 | 127479095 | |||||
chr9:127479160 | C | T | 1 | a0002c0002t0001g0142 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.780+197C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 12/25 | chr9 | 127479160 | ||||||
chr9:127479257 | T | C | 2 | a0001c0003t0001g0113a0001c0003t0001g0127 | 2 | HG01952.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.781-126T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 12/25 | chr9 | 127479257 | ||||||
chr9:127479543 | T | C | 229 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(226): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.903+38T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 13/25 | chr9 | 127479543 | ||||||
chr9:127479598 | A | G | 12 | a0001c0003t0001g0011a0001c0003t0001g0043a0001c0003t0001g0101others(9): Show | 12 | HG00673.hp1 HG00741.hp1 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.903+93A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 13/25 | chr9 | 127479598 | ||||||
chr9:127479774 | A | G | 11 | a0001c0001t0001g0004a0001c0001t0001g0181a0001c0001t0001g0182others(8): Show | 12 | HG02129.hp2 NA18950.hp1 NA18955.hp1 others(9): Show |
intron_variant | MODIFIER | c.904-65A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 13/25 | chr9 | 127479774 | ||||||
chr9:127479791 | G | A | 3 | a0001c0007t0001g0275a0001c0007t0001g0276a0001c0007t0001g0278 | 3 | HG01109.hp1 HG02723.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.904-48G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 13/25 | chr9 | 127479791 | ||||||
chr9:127479830 | C | T | 97 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(94): Show | 99 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.904-9C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 13/25 | chr9 | 127479830 | ||||||
chr9:127480033 | G | A | 1 | a0001c0003t0001g0107 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1043+55G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 14/25 | chr9 | 127480033 | ||||||
chr9:127480082 | C | T | 3 | a0001c0007t0001g0275a0001c0007t0001g0276a0001c0007t0001g0278 | 3 | HG01109.hp1 HG02723.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1043+104C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 14/25 | chr9 | 127480082 | ||||||
chr9:127480593 | G | A | 1 | a0001c0001t0001g0259 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1044-590G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 14/25 | chr9 | 127480593 | ||||||
chr9:127480799 | T | G | 1 | a0002c0002t0001g0035 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1044-384T>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 14/25 | chr9 | 127480799 | ||||||
chr9:127480870 | G | A | 4 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(1): Show | 4 | HG02886.hp1 HG03041.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1044-313G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 14/25 | chr9 | 127480870 | ||||||
chr9:127480871 | G | A | 1 | a0002c0002t0001g0091 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1044-312G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 14/25 | chr9 | 127480871 | ||||||
chr9:127480953 | A | G | 1 | a0002c0002t0001g0170 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1044-230A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 14/25 | chr9 | 127480953 | ||||||
chr9:127481174 | T | C | 1 | a0001c0001t0002g0027 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1044-9T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 14/25 | chr9 | 127481174 | ||||||
chr9:127481255 | A | AT | 13 | a0001c0001t0001g0014a0001c0001t0001g0230a0001c0001t0001g0258others(10): Show | 13 | HG01099.hp2 HG02109.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.1088+44dupT | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 15/25 | INFO_REALIGN_3_PRIME | chr9 | 127481255 | |||||
chr9:127481255 | AT | A | 16 | a0001c0001t0001g0004a0001c0001t0001g0181a0001c0001t0001g0182others(13): Show | 17 | HG01884.hp2 HG02055.hp1 HG02129.hp2 others(14): Show |
intron_variant | MODIFIER | c.1088+44delT | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 15/25 | INFO_REALIGN_3_PRIME | chr9 | 127481255 | |||||
chr9:127481341 | C | T | 58 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0277others(55): Show | 60 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.1088+114C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 15/25 | chr9 | 127481341 | ||||||
chr9:127481544 | G | A | 1 | a0001c0001t0001g0274 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1088+317G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 15/25 | chr9 | 127481544 | ||||||
chr9:127481567 | G | A | 99 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(96): Show | 101 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.1088+340G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 15/25 | chr9 | 127481567 | ||||||
chr9:127481711 | T | C | 1 | a0001c0001t0001g0268 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1088+484T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 15/25 | chr9 | 127481711 | ||||||
chr9:127481734 | A | G | 2 | a0001c0001t0001g0281a0001c0001t0001g0303 | 2 | NA18978.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.1088+507A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 15/25 | chr9 | 127481734 | ||||||
chr9:127481927 | C | T | 5 | a0002c0002t0001g0091a0002c0002t0001g0093a0002c0002t0001g0103others(2): Show | 5 | HG01884.hp1 HG02109.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1088+700C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 15/25 | chr9 | 127481927 | ||||||
chr9:127481931 | T | C | 1 | a0001c0001t0001g0241 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1088+704T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 15/25 | chr9 | 127481931 | ||||||
chr9:127481950 | A | G | 1 | a0001c0001t0001g0014 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1088+723A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 15/25 | chr9 | 127481950 | ||||||
chr9:127481976 | A | T | 188 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(185): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.1088+749A>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 15/25 | chr9 | 127481976 | ||||||
chr9:127482113 | A | G | 1 | a0002c0005t0001g0018 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1089-837A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 15/25 | chr9 | 127482113 | ||||||
chr9:127482136 | A | G | 58 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0277others(55): Show | 60 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.1089-814A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 15/25 | chr9 | 127482136 | ||||||
chr9:127482140 | C | CT | 60 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0021others(57): Show | 62 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.1089-790dupT | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 15/25 | INFO_REALIGN_3_PRIME | chr9 | 127482140 | |||||
chr9:127482140 | CT | C | 92 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0017others(89): Show | 93 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.1089-790delT | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 15/25 | INFO_REALIGN_3_PRIME | chr9 | 127482140 | |||||
chr9:127482140 | CTT | C | 11 | a0001c0001t0001g0004a0001c0001t0001g0182a0001c0001t0001g0184others(8): Show | 12 | HG00639.hp2 HG02129.hp2 HG03491.hp1 others(9): Show |
intron_variant | MODIFIER | c.1089-791_1089-790d others(4): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 15/25 | INFO_REALIGN_3_PRIME | chr9 | 127482140 | |||||
chr9:127482166 | G | A | 5 | a0002c0002t0001g0106a0002c0002t0001g0109a0002c0002t0001g0133others(2): Show | 5 | HG01168.hp1 HG01169.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.1089-784G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 15/25 | chr9 | 127482166 | ||||||
chr9:127482523 | T | G | 1 | a0001c0001t0001g0207 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1089-427T>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 15/25 | chr9 | 127482523 | ||||||
chr9:127482525 | C | G | 1 | a0001c0001t0001g0328 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1089-425C>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 15/25 | chr9 | 127482525 | ||||||
chr9:127482633 | A | G | 1 | a0001c0003t0001g0111 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1089-317A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 15/25 | chr9 | 127482633 | ||||||
chr9:127482659 | A | G | 1 | a0001c0001t0001g0191 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1089-291A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 15/25 | chr9 | 127482659 | ||||||
chr9:127482910 | A | G | 1 | a0001c0001t0001g0287 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1089-40A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 15/25 | chr9 | 127482910 | ||||||
chr9:127482938 | A | G | 1 | a0002c0002t0001g0045 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1089-12A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 15/25 | chr9 | 127482938 | ||||||
chr9:127483266 | G | C | 99 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(96): Show | 101 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.1159+246G>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 16/25 | chr9 | 127483266 | ||||||
chr9:127483508 | G | T | 97 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(94): Show | 99 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.1159+488G>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 16/25 | chr9 | 127483508 | ||||||
chr9:127483512 | T | G | 3 | a0001c0007t0001g0275a0001c0007t0001g0276a0001c0007t0001g0278 | 3 | HG01109.hp1 HG02723.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1159+492T>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 16/25 | chr9 | 127483512 | ||||||
chr9:127483564 | G | C | 2 | a0004c0006t0001g0331a0004c0006t0001g0333 | 2 | NA18989.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1159+544G>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 16/25 | chr9 | 127483564 | ||||||
chr9:127483913 | CAACCTCC others(2): Show |
C | 11 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(8): Show | 11 | HG02486.hp2 HG02717.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.1159+896_1159+904d others(11): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 16/25 | INFO_REALIGN_3_PRIME | chr9 | 127483913 | |||||
chr9:127484222 | C | T | 88 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(85): Show | 90 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.1159+1202C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 16/25 | chr9 | 127484222 | ||||||
chr9:127484263 | C | CT | 133 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0012others(130): Show | 135 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.1159+1260dupT | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 16/25 | INFO_REALIGN_3_PRIME | chr9 | 127484263 | |||||
chr9:127484263 | C | CTT | 58 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0277others(55): Show | 60 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.1159+1259_1159+126 others(6): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 16/25 | INFO_REALIGN_3_PRIME | chr9 | 127484263 | |||||
chr9:127484263 | CT | C | 10 | a0001c0003t0001g0101a0002c0002t0001g0035a0002c0002t0001g0056others(7): Show | 10 | HG00280.hp1 HG01074.hp1 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1159+1260delT | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 16/25 | INFO_REALIGN_3_PRIME | chr9 | 127484263 | |||||
chr9:127484285 | C | T | 244 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(241): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.1159+1265C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 16/25 | chr9 | 127484285 | ||||||
chr9:127484381 | T | C | 230 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(227): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.1160-1355T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 16/25 | chr9 | 127484381 | ||||||
chr9:127484620 | G | A | 2 | a0001c0001t0001g0244a0001c0001t0001g0254 | 2 | NA19066.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.1160-1116G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 16/25 | chr9 | 127484620 | ||||||
chr9:127484657 | C | T | 2 | a0001c0003t0001g0173a0007c0011t0001g0174 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1160-1079C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 16/25 | chr9 | 127484657 | ||||||
chr9:127484658 | G | A | 1 | a0001c0001t0001g0225 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1160-1078G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 16/25 | chr9 | 127484658 | ||||||
chr9:127484802 | CT | C | 22 | a0001c0001t0001g0004a0001c0001t0001g0181a0001c0001t0001g0182others(19): Show | 23 | HG02129.hp2 HG02486.hp2 HG02717.hp2 others(20): Show |
intron_variant | MODIFIER | c.1160-927delT | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 16/25 | INFO_REALIGN_3_PRIME | chr9 | 127484802 | |||||
chr9:127484808 | T | TC | 69 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0017others(66): Show | 70 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.1160-928_1160-927i others(3): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 16/25 | chr9 | 127484808 | ||||||
chr9:127484809 | T | C | 2 | a0001c0001t0001g0184a0001c0001t0001g0256 | 2 | HG02145.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.1160-927T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 16/25 | chr9 | 127484809 | ||||||
chr9:127484810 | C | T | 74 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0017others(71): Show | 75 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.1160-926C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 16/25 | chr9 | 127484810 | ||||||
chr9:127484815 | T | C | 1 | a0001c0001t0001g0235 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1160-921T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 16/25 | chr9 | 127484815 | ||||||
chr9:127484835 | G | A | 1 | a0002c0002t0001g0036 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1160-901G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 16/25 | chr9 | 127484835 | ||||||
chr9:127484885 | G | A | 10 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(7): Show | 10 | HG01884.hp2 HG02451.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1160-851G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 16/25 | chr9 | 127484885 | ||||||
chr9:127484901 | G | A | 3 | a0001c0001t0002g0027a0003c0004t0002g0025a0003c0004t0002g0026 | 3 | HG02055.hp2 HG03516.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1160-835G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 16/25 | chr9 | 127484901 | ||||||
chr9:127484997 | A | G | 1 | a0002c0002t0001g0106 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1160-739A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 16/25 | chr9 | 127484997 | ||||||
chr9:127485076 | G | T | 75 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0017others(72): Show | 76 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.1160-660G>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 16/25 | chr9 | 127485076 | ||||||
chr9:127485306 | C | G | 1 | a0001c0001t0001g0261 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1160-430C>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 16/25 | chr9 | 127485306 | ||||||
chr9:127485375 | G | C | 1 | a0002c0002t0001g0155 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1160-361G>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 16/25 | chr9 | 127485375 | ||||||
chr9:127485468 | A | G | 1 | a0002c0002t0001g0142 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1160-268A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 16/25 | chr9 | 127485468 | ||||||
chr9:127485472 | C | T | 1 | a0001c0001t0001g0241 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1160-264C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 16/25 | chr9 | 127485472 | ||||||
chr9:127485562 | C | T | 1 | a0001c0003t0001g0090 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1160-174C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 16/25 | chr9 | 127485562 | ||||||
chr9:127485611 | G | T | 10 | a0002c0002t0001g0001a0002c0002t0001g0036a0002c0002t0001g0037others(7): Show | 11 | HG01109.hp2 HG02258.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.1160-125G>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 16/25 | chr9 | 127485611 | ||||||
chr9:127485619 | C | T | 1 | a0001c0003t0001g0043 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1160-117C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 16/25 | chr9 | 127485619 | ||||||
chr9:127486022 | G | A | 11 | a0001c0001t0001g0004a0001c0001t0001g0181a0001c0001t0001g0182others(8): Show | 12 | HG02129.hp2 NA18950.hp1 NA18955.hp1 others(9): Show |
intron_variant | MODIFIER | c.1259+187G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 17/25 | chr9 | 127486022 | ||||||
chr9:127486087 | T | A | 100 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(97): Show | 102 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.1259+252T>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 17/25 | chr9 | 127486087 | ||||||
chr9:127486178 | T | C | 2 | a0001c0003t0001g0173a0007c0011t0001g0174 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1259+343T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 17/25 | chr9 | 127486178 | ||||||
chr9:127486359 | G | A | 1 | a0002c0005t0001g0018 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1259+524G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 17/25 | chr9 | 127486359 | ||||||
chr9:127486366 | G | A | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1259+531G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 17/25 | chr9 | 127486366 | ||||||
chr9:127486372 | C | T | 3 | a0001c0007t0001g0275a0001c0007t0001g0276a0001c0007t0001g0278 | 3 | HG01109.hp1 HG02723.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1259+537C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 17/25 | chr9 | 127486372 | ||||||
chr9:127486606 | T | C | 140 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(137): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.1259+771T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 17/25 | chr9 | 127486606 | ||||||
chr9:127486774 | T | C | 1 | a0002c0002t0001g0161 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1260-902T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 17/25 | chr9 | 127486774 | ||||||
chr9:127486793 | A | G | 1 | a0002c0005t0001g0018 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1260-883A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 17/25 | chr9 | 127486793 | ||||||
chr9:127486833 | T | G | 2 | a0001c0003t0001g0173a0007c0011t0001g0174 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1260-843T>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 17/25 | chr9 | 127486833 | ||||||
chr9:127486865 | C | T | 188 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(185): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.1260-811C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 17/25 | chr9 | 127486865 | ||||||
chr9:127487143 | C | G | 1 | a0002c0005t0002g0028 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1260-533C>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 17/25 | chr9 | 127487143 | ||||||
chr9:127487183 | C | CA | 19 | a0001c0001t0001g0181a0001c0001t0001g0189a0001c0001t0001g0280others(16): Show | 19 | HG00323.hp2 HG00741.hp2 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.1260-476dupA | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 17/25 | INFO_REALIGN_3_PRIME | chr9 | 127487183 | |||||
chr9:127487183 | CA | C | 80 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0017others(77): Show | 81 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.1260-476delA | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 17/25 | INFO_REALIGN_3_PRIME | chr9 | 127487183 | |||||
chr9:127487200 | A | G | 1 | a0001c0001t0001g0270 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1260-476A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 17/25 | chr9 | 127487200 | ||||||
chr9:127487291 | G | A | 1 | a0001c0001t0001g0218 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1260-385G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 17/25 | chr9 | 127487291 | ||||||
chr9:127487619 | A | G | 1 | a0002c0005t0001g0018 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1260-57A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 17/25 | chr9 | 127487619 | ||||||
chr9:127487842 | C | T | 1 | a0001c0001t0001g0233 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1347+79C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 18/25 | chr9 | 127487842 | ||||||
chr9:127487843 | G | A | 2 | a0001c0003t0001g0173a0007c0011t0001g0174 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1347+80G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 18/25 | chr9 | 127487843 | ||||||
chr9:127488207 | C | T | 1 | a0002c0002t0001g0069 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1347+444C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 18/25 | chr9 | 127488207 | ||||||
chr9:127488498 | C | T | 1 | a0002c0002t0001g0123 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1347+735C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 18/25 | chr9 | 127488498 | ||||||
chr9:127488552 | G | A | 2 | a0001c0003t0001g0173a0007c0011t0001g0174 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1347+789G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 18/25 | chr9 | 127488552 | ||||||
chr9:127488599 | C | CT | 15 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0021others(12): Show | 15 | HG01884.hp2 HG02055.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.1348-832dupT | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 18/25 | INFO_REALIGN_3_PRIME | chr9 | 127488599 | |||||
chr9:127488599 | CT | C | 101 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(98): Show | 103 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.1348-832delT | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 18/25 | INFO_REALIGN_3_PRIME | chr9 | 127488599 | |||||
chr9:127488696 | C | A | 1 | a0002c0002t0001g0068 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1348-748C>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 18/25 | chr9 | 127488696 | ||||||
chr9:127488758 | T | G | 52 | a0001c0001t0001g0306a0001c0001t0001g0312a0001c0003t0001g0010others(49): Show | 52 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.1348-686T>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 18/25 | chr9 | 127488758 | ||||||
chr9:127489205 | G | A | 1 | a0002c0002t0001g0121 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1348-239G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 18/25 | chr9 | 127489205 | ||||||
chr9:127489233 | G | A | 100 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(97): Show | 102 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.1348-211G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 18/25 | chr9 | 127489233 | ||||||
chr9:127489336 | C | A | 85 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(82): Show | 87 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.1348-108C>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 18/25 | chr9 | 127489336 | ||||||
chr9:127489410 | G | A | 11 | a0001c0001t0001g0014a0001c0003t0001g0074a0001c0003t0001g0082others(8): Show | 11 | HG00140.hp2 HG00741.hp2 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.1348-34G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 18/25 | chr9 | 127489410 | ||||||
chr9:127489556 | CAG | C | 88 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(85): Show | 90 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.1422+42_1422+43del others(2): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr9 | 127489556 | |||||
chr9:127489585 | G | A | 1 | a0001c0001t0001g0295 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1422+67G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 19/25 | chr9 | 127489585 | ||||||
chr9:127489604 | G | A | 1 | a0001c0001t0001g0313 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1422+86G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 19/25 | chr9 | 127489604 | ||||||
chr9:127489645 | G | T | 1 | a0002c0002t0001g0059 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1422+127G>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 19/25 | chr9 | 127489645 | ||||||
chr9:127489647 | C | T | 3 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023 | 3 | HG02809.hp2 HG02976.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1422+129C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 19/25 | chr9 | 127489647 | ||||||
chr9:127489821 | T | C | 11 | a0001c0001t0001g0004a0001c0001t0001g0181a0001c0001t0001g0182others(8): Show | 12 | HG02129.hp2 NA18950.hp1 NA18955.hp1 others(9): Show |
intron_variant | MODIFIER | c.1422+303T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 19/25 | chr9 | 127489821 | ||||||
chr9:127489856 | C | T | 1 | a0001c0003t0001g0144 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1422+338C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 19/25 | chr9 | 127489856 | ||||||
chr9:127489876 | G | A | 1 | a0001c0001t0001g0198 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1422+358G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 19/25 | chr9 | 127489876 | ||||||
chr9:127489971 | G | C | 245 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(242): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.1422+453G>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 19/25 | chr9 | 127489971 | ||||||
chr9:127490007 | C | T | 85 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(82): Show | 87 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.1422+489C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 19/25 | chr9 | 127490007 | ||||||
chr9:127490028 | T | A | 224 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(221): Show | 228 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.1422+510T>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 19/25 | chr9 | 127490028 | ||||||
chr9:127490033 | C | T | 39 | a0002c0002t0001g0039a0002c0002t0001g0042a0002c0002t0001g0045others(36): Show | 39 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(36): Show |
intron_variant | MODIFIER | c.1422+515C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 19/25 | chr9 | 127490033 | ||||||
chr9:127490091 | G | GCTAT | 101 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(98): Show | 103 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.1422+574_1422+575i others(6): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr9 | 127490091 | |||||
chr9:127490176 | T | C | 1 | a0001c0001t0001g0022 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1422+658T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 19/25 | chr9 | 127490176 | ||||||
chr9:127490246 | T | TTTTC | 6 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(3): Show | 6 | HG01884.hp2 HG02809.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1422+756_1422+759d others(6): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr9 | 127490246 | |||||
chr9:127490246 | T | TTTTCTTT others(1): Show |
4 | a0003c0004t0001g0019a0003c0004t0001g0029a0003c0004t0001g0030others(1): Show | 4 | HG02451.hp2 HG02630.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1422+752_1422+759d others(10): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr9 | 127490246 | |||||
chr9:127490246 | TTTTC | T | 159 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(156): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.1422+756_1422+759d others(6): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr9 | 127490246 | |||||
chr9:127490378 | G | T | 1 | a0002c0002t0001g0008 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1423-837G>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 19/25 | chr9 | 127490378 | ||||||
chr9:127490602 | T | C | 2 | a0002c0002t0001g0085a0002c0002t0001g0134 | 2 | NA18957.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1423-613T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 19/25 | chr9 | 127490602 | ||||||
chr9:127491007 | G | GA | 232 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(229): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.1423-208_1423-207i others(3): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 19/25 | chr9 | 127491007 | ||||||
chr9:127491075 | G | A | 11 | a0001c0001t0001g0004a0001c0001t0001g0181a0001c0001t0001g0182others(8): Show | 12 | HG02129.hp2 NA18950.hp1 NA18955.hp1 others(9): Show |
intron_variant | MODIFIER | c.1423-140G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 19/25 | chr9 | 127491075 | ||||||
chr9:127491392 | A | G | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1503+97A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 20/25 | chr9 | 127491392 | ||||||
chr9:127491511 | C | T | 58 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0277others(55): Show | 60 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.1503+216C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 20/25 | chr9 | 127491511 | ||||||
chr9:127491652 | A | G | 100 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(97): Show | 102 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.1503+357A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 20/25 | chr9 | 127491652 | ||||||
chr9:127492108 | G | A | 16 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0021others(13): Show | 16 | HG01884.hp2 HG02055.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.1504-694G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 20/25 | chr9 | 127492108 | ||||||
chr9:127492264 | G | T | 2 | a0001c0003t0001g0173a0007c0011t0001g0174 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1504-538G>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 20/25 | chr9 | 127492264 | ||||||
chr9:127492401 | G | A | 58 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0277others(55): Show | 60 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.1504-401G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 20/25 | chr9 | 127492401 | ||||||
chr9:127493190 | T | C | 1 | a0001c0001t0001g0014 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1599+293T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 21/25 | chr9 | 127493190 | ||||||
chr9:127493227 | A | G | 55 | a0001c0001t0001g0014a0001c0001t0001g0306a0001c0001t0001g0312others(52): Show | 55 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.1599+330A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 21/25 | chr9 | 127493227 | ||||||
chr9:127493289 | C | T | 89 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0017others(86): Show | 90 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.1599+392C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 21/25 | chr9 | 127493289 | ||||||
chr9:127493439 | G | A | 1 | a0001c0001t0001g0249 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1599+542G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 21/25 | chr9 | 127493439 | ||||||
chr9:127493477 | G | A | 1 | a0001c0001t0001g0264 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1599+580G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 21/25 | chr9 | 127493477 | ||||||
chr9:127493527 | C | T | 11 | a0001c0001t0001g0004a0001c0001t0001g0181a0001c0001t0001g0182others(8): Show | 12 | HG02129.hp2 NA18950.hp1 NA18955.hp1 others(9): Show |
intron_variant | MODIFIER | c.1599+630C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 21/25 | chr9 | 127493527 | ||||||
chr9:127493531 | C | G | 232 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(229): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.1599+634C>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 21/25 | chr9 | 127493531 | ||||||
chr9:127493543 | T | C | 1 | a0008c0010t0001g0054 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1599+646T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 21/25 | chr9 | 127493543 | ||||||
chr9:127493948 | G | A | 11 | a0001c0001t0001g0014a0001c0003t0001g0074a0001c0003t0001g0082others(8): Show | 11 | HG00140.hp2 HG00741.hp2 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.1599+1051G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 21/25 | chr9 | 127493948 | ||||||
chr9:127494032 | C | T | 1 | a0001c0001t0001g0292 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1599+1135C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 21/25 | chr9 | 127494032 | ||||||
chr9:127494109 | T | C | 1 | a0001c0003t0001g0131 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1600-1211T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 21/25 | chr9 | 127494109 | ||||||
chr9:127494219 | G | A | 2 | a0001c0003t0001g0173a0007c0011t0001g0174 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1600-1101G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 21/25 | chr9 | 127494219 | ||||||
chr9:127494527 | C | T | 11 | a0001c0001t0001g0004a0001c0001t0001g0181a0001c0001t0001g0182others(8): Show | 12 | HG02129.hp2 NA18950.hp1 NA18955.hp1 others(9): Show |
intron_variant | MODIFIER | c.1600-793C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 21/25 | chr9 | 127494527 | ||||||
chr9:127494746 | C | G | 127 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(124): Show | 129 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.1600-574C>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 21/25 | chr9 | 127494746 | ||||||
chr9:127494837 | C | T | 1 | a0001c0003t0001g0043 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1600-483C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 21/25 | chr9 | 127494837 | ||||||
chr9:127494912 | G | A | 98 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(95): Show | 100 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.1600-408G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 21/25 | chr9 | 127494912 | ||||||
chr9:127494926 | G | A | 188 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(185): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.1600-394G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 21/25 | chr9 | 127494926 | ||||||
chr9:127494950 | T | G | 1 | a0001c0001t0001g0014 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1600-370T>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 21/25 | chr9 | 127494950 | ||||||
chr9:127494981 | C | T | 1 | a0002c0002t0001g0168 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1600-339C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 21/25 | chr9 | 127494981 | ||||||
chr9:127495123 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1600-197G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 21/25 | chr9 | 127495123 | ||||||
chr9:127495153 | A | G | 1 | a0002c0005t0001g0215 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1600-167A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 21/25 | chr9 | 127495153 | ||||||
chr9:127495168 | G | A | 3 | a0001c0001t0001g0012a0001c0001t0001g0013a0003c0004t0001g0015 | 3 | HG03041.hp1 HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1600-152G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 21/25 | chr9 | 127495168 | ||||||
chr9:127495180 | C | T | 1 | a0003c0004t0001g0015 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1600-140C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 21/25 | chr9 | 127495180 | ||||||
chr9:127495208 | C | A | 1 | a0002c0005t0001g0018 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1600-112C>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 21/25 | chr9 | 127495208 | ||||||
chr9:127495211 | C | G | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1600-109C>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 21/25 | chr9 | 127495211 | ||||||
chr9:127495214 | A | G | 1 | a0001c0003t0001g0082 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1600-106A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 21/25 | chr9 | 127495214 | ||||||
chr9:127495288 | G | A | 1 | a0001c0001t0001g0204 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1600-32G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 21/25 | chr9 | 127495288 | ||||||
chr9:127495657 | A | G | 11 | a0001c0001t0001g0004a0001c0001t0001g0181a0001c0001t0001g0182others(8): Show | 12 | HG02129.hp2 NA18950.hp1 NA18955.hp1 others(9): Show |
intron_variant | MODIFIER | c.1698+239A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 22/25 | chr9 | 127495657 | ||||||
chr9:127495673 | C | T | 1 | a0001c0001t0001g0014 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1698+255C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 22/25 | chr9 | 127495673 | ||||||
chr9:127495796 | G | A | 3 | a0001c0001t0002g0027a0003c0004t0002g0025a0003c0004t0002g0026 | 3 | HG02055.hp2 HG03516.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1699-168G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 22/25 | chr9 | 127495796 | ||||||
chr9:127495881 | A | T | 100 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(97): Show | 102 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.1699-83A>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 22/25 | chr9 | 127495881 | ||||||
chr9:127496101 | C | T | 6 | a0002c0002t0001g0050a0002c0002t0001g0051a0002c0002t0001g0056others(3): Show | 6 | HG00280.hp1 HG01258.hp2 HG01358.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.1830+6C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 23/25 | chr9 | 127496101 | ||||||
chr9:127496131 | C | T | 11 | a0001c0001t0001g0004a0001c0001t0001g0181a0001c0001t0001g0182others(8): Show | 12 | HG02129.hp2 NA18950.hp1 NA18955.hp1 others(9): Show |
intron_variant | MODIFIER | c.1830+36C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 23/25 | chr9 | 127496131 | ||||||
chr9:127496515 | C | T | 12 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(9): Show | 12 | HG02486.hp2 HG02717.hp2 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.1830+420C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 23/25 | chr9 | 127496515 | ||||||
chr9:127496552 | G | A | 2 | a0002c0002t0001g0048a0002c0002t0005g0046 | 2 | HG01192.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.1830+457G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 23/25 | chr9 | 127496552 | ||||||
chr9:127496631 | A | C | 1 | a0001c0001t0001g0288 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1830+536A>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 23/25 | chr9 | 127496631 | ||||||
chr9:127496726 | G | A | 1 | a0002c0005t0002g0028 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1831-527G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 23/25 | chr9 | 127496726 | ||||||
chr9:127496732 | G | A | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1831-521G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 23/25 | chr9 | 127496732 | ||||||
chr9:127496818 | A | T | 75 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(72): Show | 77 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.1831-435A>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 23/25 | chr9 | 127496818 | ||||||
chr9:127496837 | C | T | 1 | a0001c0003t0001g0105 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1831-416C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 23/25 | chr9 | 127496837 | ||||||
chr9:127496869 | T | C | 3 | a0001c0007t0001g0275a0001c0007t0001g0276a0001c0007t0001g0278 | 3 | HG01109.hp1 HG02723.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1831-384T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 23/25 | chr9 | 127496869 | ||||||
chr9:127497031 | T | C | 11 | a0001c0001t0001g0004a0001c0001t0001g0181a0001c0001t0001g0182others(8): Show | 12 | HG02129.hp2 NA18950.hp1 NA18955.hp1 others(9): Show |
intron_variant | MODIFIER | c.1831-222T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 23/25 | chr9 | 127497031 | ||||||
chr9:127497187 | C | T | 3 | a0001c0007t0001g0275a0001c0007t0001g0276a0001c0007t0001g0278 | 3 | HG01109.hp1 HG02723.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1831-66C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 23/25 | chr9 | 127497187 | ||||||
chr9:127497195 | A | G | 4 | a0003c0004t0001g0019a0003c0004t0001g0029a0003c0004t0001g0030others(1): Show | 4 | HG02451.hp2 HG02630.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1831-58A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 23/25 | chr9 | 127497195 | ||||||
chr9:127497206 | C | T | 2 | a0001c0003t0001g0173a0007c0011t0001g0174 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1831-47C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 23/25 | chr9 | 127497206 | ||||||
chr9:127497339 | A | C | 232 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(229): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(233): Show |
splice_region_variant&intron_variant | LOW | c.1912+5A>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127497339 | ||||||
chr9:127497369 | C | T | 1 | a0002c0002t0001g0140 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1912+35C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127497369 | ||||||
chr9:127497377 | G | A | 58 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0277others(55): Show | 60 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.1912+43G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127497377 | ||||||
chr9:127497479 | A | G | 1 | a0003c0004t0002g0025 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1912+145A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127497479 | ||||||
chr9:127497551 | C | A | 11 | a0001c0001t0001g0014a0001c0003t0001g0074a0001c0003t0001g0082others(8): Show | 11 | HG00140.hp2 HG00741.hp2 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.1912+217C>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127497551 | ||||||
chr9:127497681 | C | T | 2 | a0001c0001t0001g0193a0001c0001t0001g0201 | 2 | HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1912+347C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127497681 | ||||||
chr9:127498185 | C | T | 3 | a0001c0007t0001g0275a0001c0007t0001g0276a0001c0007t0001g0278 | 3 | HG01109.hp1 HG02723.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1912+851C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127498185 | ||||||
chr9:127498381 | A | C | 11 | a0001c0001t0001g0004a0001c0001t0001g0181a0001c0001t0001g0182others(8): Show | 12 | HG02129.hp2 NA18950.hp1 NA18955.hp1 others(9): Show |
intron_variant | MODIFIER | c.1912+1047A>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127498381 | ||||||
chr9:127498492 | C | A | 2 | a0001c0001t0001g0016a0001c0001t0001g0017 | 2 | HG02258.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1912+1158C>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127498492 | ||||||
chr9:127498509 | C | T | 97 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(94): Show | 99 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.1912+1175C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127498509 | ||||||
chr9:127498536 | C | T | 2 | a0001c0001t0001g0016a0001c0001t0001g0017 | 2 | HG02258.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1912+1202C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127498536 | ||||||
chr9:127498611 | G | A | 11 | a0001c0001t0001g0004a0001c0001t0001g0181a0001c0001t0001g0182others(8): Show | 12 | HG02129.hp2 NA18950.hp1 NA18955.hp1 others(9): Show |
intron_variant | MODIFIER | c.1912+1277G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127498611 | ||||||
chr9:127498638 | G | A | 1 | a0001c0001t0001g0198 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1912+1304G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127498638 | ||||||
chr9:127498650 | T | C | 10 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(7): Show | 10 | HG01884.hp2 HG02451.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1912+1316T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127498650 | ||||||
chr9:127498806 | C | T | 74 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0017others(71): Show | 75 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.1912+1472C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127498806 | ||||||
chr9:127498834 | G | A | 11 | a0001c0001t0001g0014a0001c0003t0001g0074a0001c0003t0001g0082others(8): Show | 11 | HG00140.hp2 HG00741.hp2 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.1912+1500G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127498834 | ||||||
chr9:127498849 | A | G | 1 | a0001c0001t0001g0266 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1912+1515A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127498849 | ||||||
chr9:127498931 | C | T | 1 | a0001c0001t0001g0243 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1912+1597C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127498931 | ||||||
chr9:127499055 | C | CA | 11 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(8): Show | 11 | HG02717.hp2 HG02723.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1912+1733dupA | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr9 | 127499055 | |||||
chr9:127499055 | C | CAA | 64 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0017others(61): Show | 65 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.1912+1732_1912+173 others(6): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr9 | 127499055 | |||||
chr9:127499055 | C | CAAA | 10 | a0001c0001t0001g0208a0001c0001t0001g0251a0001c0001t0001g0258others(7): Show | 10 | HG01099.hp2 HG02280.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1912+1731_1912+173 others(7): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr9 | 127499055 | |||||
chr9:127499099 | T | C | 1 | a0002c0005t0001g0018 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1912+1765T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127499099 | ||||||
chr9:127499141 | C | T | 2 | a0001c0003t0001g0173a0007c0011t0001g0174 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1912+1807C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127499141 | ||||||
chr9:127499270 | G | A | 1 | a0001c0001t0001g0258 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1913-1740G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127499270 | ||||||
chr9:127499283 | A | G | 2 | a0002c0002t0001g0076a0002c0002t0001g0175 | 2 | NA18991.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.1913-1727A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127499283 | ||||||
chr9:127499524 | C | T | 58 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0277others(55): Show | 60 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.1913-1486C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127499524 | ||||||
chr9:127499529 | T | TAA | 10 | a0001c0001t0001g0004a0001c0001t0001g0181a0001c0001t0001g0182others(7): Show | 11 | HG02129.hp2 NA18950.hp1 NA18955.hp1 others(8): Show |
intron_variant | MODIFIER | c.1913-1473_1913-147 others(6): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr9 | 127499529 | |||||
chr9:127499529 | TA | T | 53 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0279others(50): Show | 55 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.1913-1472delA | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr9 | 127499529 | |||||
chr9:127499537 | A | T | 3 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0003t0001g0087 | 3 | HG03041.hp1 HG03471.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.1913-1473A>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127499537 | ||||||
chr9:127499538 | AT | A | 110 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0016others(107): Show | 111 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.1913-1471delT | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127499538 | ||||||
chr9:127499539 | T | A | 22 | a0001c0001t0001g0004a0001c0001t0001g0181a0001c0001t0001g0182others(19): Show | 23 | HG01109.hp1 HG01433.hp2 HG01978.hp1 others(20): Show |
intron_variant | MODIFIER | c.1913-1471T>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127499539 | ||||||
chr9:127499541 | T | A | 95 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(92): Show | 97 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.1913-1469T>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127499541 | ||||||
chr9:127499543 | T | A | 3 | a0001c0007t0001g0275a0001c0007t0001g0276a0001c0007t0001g0278 | 3 | HG01109.hp1 HG02723.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1913-1467T>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127499543 | ||||||
chr9:127499556 | A | G | 1 | a0002c0005t0001g0018 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1913-1454A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127499556 | ||||||
chr9:127499569 | C | T | 11 | a0001c0001t0001g0004a0001c0001t0001g0181a0001c0001t0001g0182others(8): Show | 12 | HG02129.hp2 NA18950.hp1 NA18955.hp1 others(9): Show |
intron_variant | MODIFIER | c.1913-1441C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127499569 | ||||||
chr9:127499652 | C | T | 2 | a0001c0001t0001g0016a0001c0001t0001g0017 | 2 | HG02258.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1913-1358C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127499652 | ||||||
chr9:127499797 | A | G | 184 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(181): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.1913-1213A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127499797 | ||||||
chr9:127499810 | C | T | 1 | a0001c0003t0001g0131 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1913-1200C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127499810 | ||||||
chr9:127499873 | C | T | 1 | a0001c0001t0001g0230 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1913-1137C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127499873 | ||||||
chr9:127499925 | A | G | 2 | a0001c0001t0001g0197a0001c0001t0001g0200 | 2 | HG02818.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1913-1085A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127499925 | ||||||
chr9:127499933 | A | G | 3 | a0001c0003t0001g0165a0003c0004t0001g0020a0003c0004t0001g0024 | 3 | HG01884.hp2 HG02976.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1913-1077A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127499933 | ||||||
chr9:127500140 | C | G | 1 | a0002c0002t0001g0032 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1913-870C>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127500140 | ||||||
chr9:127500150 | CA | C | 99 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(96): Show | 101 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.1913-856delA | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr9 | 127500150 | |||||
chr9:127500151 | A | G | 1 | a0002c0005t0001g0018 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1913-859A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127500151 | ||||||
chr9:127500155 | G | T | 99 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(96): Show | 101 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.1913-855G>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127500155 | ||||||
chr9:127500310 | G | A | 2 | a0002c0002t0001g0064a0002c0002t0001g0065 | 2 | HG03831.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1913-700G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127500310 | ||||||
chr9:127500318 | G | A | 187 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(184): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.1913-692G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127500318 | ||||||
chr9:127500351 | A | ACT | 184 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(181): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.1913-658_1913-657d others(4): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr9 | 127500351 | |||||
chr9:127500358 | C | CAAAAA | 54 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0277others(51): Show | 56 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.1913-639_1913-635d others(7): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr9 | 127500358 | |||||
chr9:127500358 | C | CAAAAAAA others(3): Show |
3 | a0001c0001t0001g0021a0001c0001t0001g0255a0001c0001t0001g0256 | 3 | HG02145.hp2 HG02717.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1913-644_1913-635d others(12): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr9 | 127500358 | |||||
chr9:127500358 | C | CAAAAAAA others(4): Show |
23 | a0001c0001t0001g0016a0001c0001t0001g0022a0001c0001t0001g0023others(20): Show | 23 | HG01168.hp2 HG02451.hp2 HG02630.hp1 others(20): Show |
intron_variant | MODIFIER | c.1913-645_1913-635d others(13): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr9 | 127500358 | |||||
chr9:127500358 | C | CAAAAAAA others(5): Show |
61 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0199others(58): Show | 62 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.1913-646_1913-635d others(14): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr9 | 127500358 | |||||
chr9:127500358 | C | CAAAAAAA others(6): Show |
10 | a0001c0001t0001g0204a0001c0001t0001g0209a0001c0001t0001g0218others(7): Show | 10 | HG01071.hp2 HG01256.hp2 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.1913-647_1913-635d others(15): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr9 | 127500358 | |||||
chr9:127500358 | C | CAAAAAAA others(7): Show |
8 | a0001c0001t0001g0247a0001c0003t0001g0074a0001c0003t0001g0082others(5): Show | 8 | HG00140.hp2 HG01070.hp1 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.1913-648_1913-635d others(16): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr9 | 127500358 | |||||
chr9:127500358 | C | CAAAAAAA others(8): Show |
2 | a0001c0003t0001g0096a0001c0003t0001g0152 | 2 | HG00741.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.1913-649_1913-635d others(17): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr9 | 127500358 | |||||
chr9:127500358 | C | CAAAAAAA others(9): Show |
1 | a0001c0001t0001g0014 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1913-650_1913-635d others(18): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr9 | 127500358 | |||||
chr9:127500358 | CA | C | 8 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0007t0001g0275others(5): Show | 8 | HG01109.hp1 HG02723.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.1913-635delA | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr9 | 127500358 | |||||
chr9:127500374 | A | AAAAAAAA others(4): Show |
3 | a0001c0001t0001g0181a0001c0001t0001g0189a0001c0001t0001g0190 | 3 | NA18959.hp2 NA18991.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.1913-635_1913-634i others(13): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr9 | 127500374 | |||||
chr9:127500374 | A | AAAAAAAA others(3): Show |
7 | a0001c0001t0001g0004a0001c0001t0001g0182a0001c0001t0001g0183others(4): Show | 8 | HG02129.hp2 NA18950.hp1 NA18955.hp1 others(5): Show |
intron_variant | MODIFIER | c.1913-635_1913-634i others(12): Show |
LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr9 | 127500374 | |||||
chr9:127500543 | A | T | 1 | a0001c0001t0001g0182 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1913-467A>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127500543 | ||||||
chr9:127500761 | C | T | 12 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(9): Show | 12 | HG02486.hp2 HG02717.hp2 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.1913-249C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127500761 | ||||||
chr9:127500821 | G | A | 12 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(9): Show | 12 | HG02486.hp2 HG02717.hp2 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.1913-189G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 24/25 | chr9 | 127500821 | ||||||
chr9:127501175 | C | T | 11 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(8): Show | 11 | HG02486.hp2 HG02717.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.2046+32C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 25/25 | chr9 | 127501175 | ||||||
chr9:127501227 | G | A | 1 | a0001c0003t0001g0153 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2046+84G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 25/25 | chr9 | 127501227 | ||||||
chr9:127501548 | A | G | 1 | a0001c0003t0001g0082 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2046+405A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 25/25 | chr9 | 127501548 | ||||||
chr9:127501623 | T | C | 1 | a0001c0001t0001g0223 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2046+480T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 25/25 | chr9 | 127501623 | ||||||
chr9:127501678 | G | T | 1 | a0001c0001t0001g0021 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2046+535G>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 25/25 | chr9 | 127501678 | ||||||
chr9:127501682 | A | G | 1 | a0001c0001t0001g0213 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2046+539A>G | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 25/25 | chr9 | 127501682 | ||||||
chr9:127501774 | A | T | 1 | a0001c0001t0001g0277 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2046+631A>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 25/25 | chr9 | 127501774 | ||||||
chr9:127501881 | G | A | 2 | a0001c0003t0001g0173a0007c0011t0001g0174 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2046+738G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 25/25 | chr9 | 127501881 | ||||||
chr9:127501888 | G | A | 1 | a0001c0001t0001g0017 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2046+745G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 25/25 | chr9 | 127501888 | ||||||
chr9:127502053 | C | T | 2 | a0001c0003t0001g0173a0007c0011t0001g0174 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2047-721C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 25/25 | chr9 | 127502053 | ||||||
chr9:127502061 | G | A | 12 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(9): Show | 12 | HG02486.hp2 HG02717.hp2 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.2047-713G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 25/25 | chr9 | 127502061 | ||||||
chr9:127502151 | G | A | 3 | a0001c0001t0001g0204a0001c0001t0001g0210a0002c0002t0001g0128 | 3 | HG01168.hp2 HG01517.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.2047-623G>A | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 25/25 | chr9 | 127502151 | ||||||
chr9:127502207 | T | C | 1 | a0002c0002t0001g0128 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2047-567T>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 25/25 | chr9 | 127502207 | ||||||
chr9:127502466 | C | T | 1 | a0002c0005t0001g0018 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2047-308C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 25/25 | chr9 | 127502466 | ||||||
chr9:127502686 | C | CA | 24 | a0001c0003t0001g0033a0001c0003t0001g0110a0001c0003t0001g0118others(21): Show | 24 | HG00140.hp1 HG00741.hp1 HG01175.hp1 others(21): Show |
intron_variant | MODIFIER | c.2047-64dupA | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr9 | 127502686 | |||||
chr9:127502686 | CA | C | 160 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(157): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.2047-64delA | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr9 | 127502686 | |||||
chr9:127502735 | C | T | 53 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0277others(50): Show | 55 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.2047-39C>T | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 25/25 | chr9 | 127502735 | ||||||
chr9:127502751 | A | C | 1 | a0001c0001t0001g0198 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2047-23A>C | LRSAM1 | ENSG00000148356.15 | transcript | ENST00000300417.11 | protein_coding | 25/25 | chr9 | 127502751 |