geneid | 7248 |
---|---|
ensemblid | ENSG00000165699.15 |
hgncid | 12362 |
symbol | TSC1 |
name | TSC complex subunit 1 |
refseq_nuc | NM_000368.5 |
refseq_prot | NP_000359.1 |
ensembl_nuc | ENST00000298552.9 |
ensembl_prot | ENSP00000298552.3 |
mane_status | MANE Select |
chr | chr9 |
start | 132891349 |
end | 132944616 |
strand | - |
ver | v1.2 |
region | chr9:132891349-132944616 |
region5000 | chr9:132886349-132949616 |
regionname0 | TSC1_chr9_132891349_132944616 |
regionname5000 | TSC1_chr9_132886349_132949616 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1164 | 277 | 61 | 51 | 133 | 6 | 24 | 100 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0002 | 0/0 | 1164 | 42 | 22 | 4 | 12 | 2 | 2 | 9 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0003 | 0/0 | 1164 | 9 | 0 | 9 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0004 | 0/0 | 1164 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0005 | 0/0 | 1164 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0006 | 0/0 | 1164 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0007 | 0/0 | 1164 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0008 | 0/0 | 1164 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0009 | 0/0 | 1164 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 3495 | 234 | 53 | 36 | 114 | 6 | 24 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
c0002 | 0/0 | 3495 | 39 | 19 | 4 | 12 | 2 | 2 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
c0003 | 0/1 | 3495 | 17 | 4 | 8 | 4 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
c0004 | 0/0 | 3495 | 9 | 0 | 0 | 9 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
c0005 | 0/0 | 3495 | 9 | 0 | 9 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
c0006 | 0/0 | 3495 | 8 | 0 | 7 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
c0007 | 0/0 | 3495 | 4 | 4 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
c0008 | 0/0 | 3495 | 3 | 0 | 0 | 3 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
c0009 | 0/0 | 3495 | 2 | 2 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
c0010 | 0/0 | 3495 | 2 | 2 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
c0011 | 0/0 | 3495 | 2 | 2 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
c0012 | 0/0 | 3495 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
c0013 | 0/0 | 3495 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
c0014 | 0/0 | 3495 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
c0015 | 0/0 | 3495 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
c0016 | 0/0 | 3495 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
c0017 | 0/0 | 3495 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
c0018 | 0/0 | 3495 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 5103 | 97 | 6 | 25 | 55 | 2 | 9 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0002 | 1/0 | 5104 | 32 | 1 | 8 | 20 | 0 | 2 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0003 | 0/0 | 5104 | 20 | 3 | 0 | 15 | 2 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0004 | 0/0 | 5104 | 9 | 0 | 3 | 6 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0005 | 0/0 | 5104 | 7 | 5 | 2 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0006 | 0/0 | 5104 | 7 | 7 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0007 | 0/0 | 5105 | 7 | 7 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0008 | 0/0 | 5102 | 6 | 0 | 0 | 5 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0009 | 0/0 | 5104 | 6 | 0 | 1 | 5 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0010 | 0/0 | 5104 | 6 | 0 | 0 | 5 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0011 | 0/0 | 5104 | 5 | 4 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0012 | 0/0 | 5104 | 4 | 0 | 0 | 4 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0013 | 0/0 | 5104 | 4 | 3 | 0 | 0 | 1 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0014 | 0/0 | 5104 | 4 | 4 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0015 | 0/0 | 5105 | 3 | 3 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0016 | 0/0 | 5105 | 3 | 0 | 0 | 3 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0017 | 0/0 | 5103 | 3 | 0 | 1 | 0 | 1 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0018 | 0/0 | 5103 | 3 | 0 | 2 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0019 | 0/0 | 5104 | 3 | 3 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0020 | 0/0 | 5105 | 3 | 1 | 1 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0021 | 0/0 | 5104 | 3 | 0 | 0 | 3 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0022 | 0/0 | 5102 | 2 | 2 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0023 | 0/0 | 5103 | 2 | 0 | 1 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0024 | 0/0 | 5103 | 2 | 0 | 0 | 0 | 0 | 2 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0025 | 0/0 | 5103 | 2 | 0 | 0 | 2 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0026 | 0/0 | 5104 | 2 | 0 | 0 | 2 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0027 | 0/0 | 5104 | 2 | 2 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0028 | 0/0 | 5104 | 2 | 0 | 0 | 1 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0029 | 0/0 | 5103 | 2 | 2 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0030 | 0/0 | 5103 | 2 | 2 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0031 | 0/0 | 5104 | 2 | 0 | 2 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0032 | 0/0 | 5103 | 2 | 2 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0033 | 0/0 | 5105 | 2 | 1 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0034 | 0/0 | 5105 | 2 | 2 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0035 | 0/0 | 5104 | 2 | 0 | 2 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0036 | 0/0 | 5104 | 2 | 0 | 0 | 2 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0037 | 0/0 | 5104 | 2 | 2 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0038 | 0/0 | 5103 | 2 | 2 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0039 | 0/0 | 5104 | 2 | 0 | 0 | 0 | 1 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0040 | 0/0 | 5104 | 2 | 0 | 1 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0041 | 0/0 | 5106 | 2 | 2 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0042 | 0/0 | 5103 | 2 | 0 | 0 | 1 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0043 | 0/0 | 5103 | 2 | 2 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0044 | 0/0 | 5103 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0045 | 0/0 | 5104 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0046 | 0/0 | 5103 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0047 | 0/0 | 5103 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0048 | 0/0 | 5103 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0049 | 0/0 | 5103 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0050 | 0/0 | 5103 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0051 | 0/0 | 5103 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0052 | 0/0 | 5103 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0053 | 0/0 | 5103 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0054 | 0/0 | 5102 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0055 | 0/0 | 5104 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0056 | 0/0 | 5103 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0057 | 0/0 | 5105 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0058 | 0/0 | 5105 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0059 | 0/0 | 5104 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0060 | 0/0 | 5104 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0061 | 0/0 | 5104 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0062 | 0/0 | 5105 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0063 | 0/0 | 5103 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0064 | 0/0 | 5104 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0065 | 0/0 | 5104 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0066 | 0/0 | 5105 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0067 | 0/0 | 5105 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0068 | 0/0 | 5103 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0069 | 0/0 | 5104 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0070 | 0/0 | 5104 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0071 | 0/0 | 5104 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0072 | 0/0 | 5104 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0073 | 0/0 | 5104 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0074 | 0/0 | 5104 | 1 | 0 | 0 | 0 | 1 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0075 | 0/0 | 5105 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0076 | 0/0 | 5104 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0077 | 0/0 | 5105 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0078 | 0/0 | 5105 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0079 | 0/0 | 5106 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0080 | 0/0 | 5103 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0081 | 0/0 | 5104 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0082 | 0/0 | 5105 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0083 | 0/0 | 5106 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0084 | 0/1 | 5104 | 1 | 0 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0085 | 0/0 | 5103 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0086 | 0/0 | 5104 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0087 | 0/0 | 5105 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0088 | 0/0 | 5104 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0089 | 0/0 | 5104 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0090 | 0/0 | 5106 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0091 | 0/0 | 5104 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0092 | 0/0 | 5104 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0093 | 0/0 | 5106 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0094 | 0/0 | 5104 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0095 | 0/0 | 5105 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0096 | 0/0 | 5104 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0097 | 0/0 | 5104 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0098 | 0/0 | 5105 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0099 | 0/0 | 5104 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
t0100 | 0/0 | 5106 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 10 | 0 | 4 | 3 | 0 | 3 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0004 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0007 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0011 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0017 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0018 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0019 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0020 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0048 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0283 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 3495 | 234 | 53 | 36 | 114 | 6 | 24 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0003 | 0/1 | 3495 | 17 | 4 | 8 | 4 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0004 | 0/0 | 3495 | 9 | 0 | 0 | 9 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0006 | 0/0 | 3495 | 8 | 0 | 7 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0007 | 0/0 | 3495 | 4 | 4 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0008 | 0/0 | 3495 | 3 | 0 | 0 | 3 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0015 | 0/0 | 3495 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0018 | 0/0 | 3495 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0002c0002 | 0/0 | 3495 | 39 | 19 | 4 | 12 | 2 | 2 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0002c0009 | 0/0 | 3495 | 2 | 2 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0002c0013 | 0/0 | 3495 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0003c0005 | 0/0 | 3495 | 9 | 0 | 9 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0004c0011 | 0/0 | 3495 | 2 | 2 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0005c0010 | 0/0 | 3495 | 2 | 2 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0006c0017 | 0/0 | 3495 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0007c0016 | 0/0 | 3495 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0008c0014 | 0/0 | 3495 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0009c0012 | 0/0 | 3495 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 8597 | 86 | 6 | 17 | 52 | 2 | 9 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0001t0002 | 1/0 | 8598 | 25 | 1 | 2 | 19 | 0 | 2 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0001t0003 | 0/0 | 8598 | 10 | 0 | 0 | 8 | 2 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0001t0004 | 0/0 | 8598 | 8 | 0 | 2 | 6 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0001t0005 | 0/0 | 8598 | 5 | 4 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0001t0006 | 0/0 | 8598 | 5 | 5 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0001t0007 | 0/0 | 8599 | 5 | 5 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0001t0008 | 0/0 | 8596 | 6 | 0 | 0 | 5 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0001t0010 | 0/0 | 8598 | 5 | 0 | 0 | 4 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0001t0011 | 0/0 | 8598 | 4 | 4 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0001t0012 | 0/0 | 8598 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0001t0013 | 0/0 | 8598 | 2 | 2 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0001t0015 | 0/0 | 8599 | 3 | 3 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0001t0016 | 0/0 | 8599 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0001t0017 | 0/0 | 8597 | 3 | 0 | 1 | 0 | 1 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0001t0018 | 0/0 | 8597 | 3 | 0 | 2 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0001t0019 | 0/0 | 8598 | 3 | 3 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0001t0020 | 0/0 | 8599 | 2 | 1 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0001t0021 | 0/0 | 8598 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0001t0022 | 0/0 | 8596 | 2 | 2 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0001t0023 | 0/0 | 8597 | 2 | 0 | 1 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0001t0024 | 0/0 | 8597 | 2 | 0 | 0 | 0 | 0 | 2 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0001t0025 | 0/0 | 8597 | 2 | 0 | 0 | 2 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0001t0027 | 0/0 | 8598 | 2 | 2 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0001t0028 | 0/0 | 8598 | 2 | 0 | 0 | 1 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0001t0033 | 0/0 | 8599 | 2 | 1 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0001t0034 | 0/0 | 8599 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0001t0036 | 0/0 | 8598 | 2 | 0 | 0 | 2 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0001t0037 | 0/0 | 8598 | 2 | 2 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0001t0039 | 0/0 | 8598 | 2 | 0 | 0 | 0 | 1 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0001t0040 | 0/0 | 8598 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0001t0041 | 0/0 | 8600 | 2 | 2 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0001t0042 | 0/0 | 8597 | 2 | 0 | 0 | 1 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0001t0044 | 0/0 | 8597 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0001t0045 | 0/0 | 8598 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0001t0046 | 0/0 | 8597 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0001t0047 | 0/0 | 8597 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0001t0048 | 0/0 | 8597 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0001t0049 | 0/0 | 8597 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0001t0050 | 0/0 | 8597 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0001t0051 | 0/0 | 8597 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0001t0052 | 0/0 | 8597 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0001t0053 | 0/0 | 8597 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0001t0054 | 0/0 | 8596 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0001t0055 | 0/0 | 8598 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0001t0056 | 0/0 | 8597 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0001t0061 | 0/0 | 8598 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0001t0062 | 0/0 | 8599 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0001t0063 | 0/0 | 8597 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0001t0068 | 0/0 | 8597 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0001t0071 | 0/0 | 8598 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0001t0078 | 0/0 | 8599 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0001t0082 | 0/0 | 8599 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0001t0083 | 0/0 | 8600 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0001t0085 | 0/0 | 8597 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0001t0088 | 0/0 | 8598 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0001t0090 | 0/0 | 8600 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0001t0091 | 0/0 | 8598 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0001t0092 | 0/0 | 8598 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0001t0094 | 0/0 | 8598 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0001t0095 | 0/0 | 8599 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0001t0096 | 0/0 | 8598 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0001t0099 | 0/0 | 8598 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0003t0009 | 0/0 | 8598 | 3 | 0 | 1 | 2 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0003t0011 | 0/0 | 8598 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0003t0030 | 0/0 | 8597 | 2 | 2 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0003t0031 | 0/0 | 8598 | 2 | 0 | 2 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0003t0035 | 0/0 | 8598 | 2 | 0 | 2 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0003t0060 | 0/0 | 8598 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0003t0076 | 0/0 | 8598 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0003t0077 | 0/0 | 8599 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0003t0079 | 0/0 | 8600 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0003t0081 | 0/0 | 8598 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0003t0084 | 0/1 | 8598 | 1 | 0 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0003t0097 | 0/0 | 8598 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0004t0003 | 0/0 | 8598 | 6 | 0 | 0 | 6 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0004t0010 | 0/0 | 8598 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0004t0021 | 0/0 | 8598 | 2 | 0 | 0 | 2 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0006t0002 | 0/0 | 8598 | 7 | 0 | 6 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0006t0020 | 0/0 | 8599 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0007t0005 | 0/0 | 8598 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0007t0006 | 0/0 | 8598 | 2 | 2 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0007t0064 | 0/0 | 8598 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0008t0009 | 0/0 | 8598 | 2 | 0 | 0 | 2 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0008t0089 | 0/0 | 8598 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0015t0003 | 0/0 | 8598 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0001c0018t0009 | 0/0 | 8598 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0002c0002t0003 | 0/0 | 8598 | 3 | 3 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0002c0002t0005 | 0/0 | 8598 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0002c0002t0012 | 0/0 | 8598 | 3 | 0 | 0 | 3 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0002c0002t0013 | 0/0 | 8598 | 1 | 0 | 0 | 0 | 1 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0002c0002t0014 | 0/0 | 8598 | 4 | 4 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0002c0002t0016 | 0/0 | 8599 | 2 | 0 | 0 | 2 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0002c0002t0026 | 0/0 | 8598 | 2 | 0 | 0 | 2 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0002c0002t0029 | 0/0 | 8597 | 2 | 2 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0002c0002t0032 | 0/0 | 8597 | 2 | 2 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0002c0002t0034 | 0/0 | 8599 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0002c0002t0038 | 0/0 | 8597 | 2 | 2 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0002c0002t0040 | 0/0 | 8598 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0002c0002t0057 | 0/0 | 8599 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0002c0002t0058 | 0/0 | 8599 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0002c0002t0059 | 0/0 | 8598 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0002c0002t0065 | 0/0 | 8598 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0002c0002t0066 | 0/0 | 8599 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0002c0002t0067 | 0/0 | 8599 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0002c0002t0069 | 0/0 | 8598 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0002c0002t0070 | 0/0 | 8598 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0002c0002t0072 | 0/0 | 8598 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0002c0002t0073 | 0/0 | 8598 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0002c0002t0074 | 0/0 | 8598 | 1 | 0 | 0 | 0 | 1 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0002c0002t0075 | 0/0 | 8599 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0002c0002t0080 | 0/0 | 8597 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0002c0002t0086 | 0/0 | 8598 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0002c0002t0098 | 0/0 | 8599 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0002c0009t0093 | 0/0 | 8600 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0002c0009t0100 | 0/0 | 8600 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0002c0013t0087 | 0/0 | 8599 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0003c0005t0001 | 0/0 | 8597 | 8 | 0 | 8 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0003c0005t0004 | 0/0 | 8598 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0004c0011t0007 | 0/0 | 8599 | 2 | 2 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0005c0010t0043 | 0/0 | 8597 | 2 | 2 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0006c0017t0001 | 0/0 | 8597 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0007c0016t0001 | 0/0 | 8597 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0008c0014t0001 | 0/0 | 8597 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
a0009c0012t0013 | 0/0 | 8598 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | copy fasta | chr9 | 132886349 | 132949616 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 10 | 0 | 4 | 3 | 0 | 3 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0001g0004 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0001g0017 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0001g0018 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0001g0020 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0002g0011 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0002g0048 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0003g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0003g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0003g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0004g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0004g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0004g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0004g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0004g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0004g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0004g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0004g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0005g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0005g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0005g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0005g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0005g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0006g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0006g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0006g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0006g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0006g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0007g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0007g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0007g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0007g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0007g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0008g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0008g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0008g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0008g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0008g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0008g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0010g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0010g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0010g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0010g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0010g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0011g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0011g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0011g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0011g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0012g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0013g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0013g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0015g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0015g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0015g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0016g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0017g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0017g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0017g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0018g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0018g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0018g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0019g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0019g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0019g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0020g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0020g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0021g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0022g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0022g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0023g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0023g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0024g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0024g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0025g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0025g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0027g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0027g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0028g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0028g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0033g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0033g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0034g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0036g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0037g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0037g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0039g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0039g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0040g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0041g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0041g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0042g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0042g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0044g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0045g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0046g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0047g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0048g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0049g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0050g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0051g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0052g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0053g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0054g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0055g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0056g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0061g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0062g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0063g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0068g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0071g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0078g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0082g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0083g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0085g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0088g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0090g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0091g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0092g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0094g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0095g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0096g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0001t0099g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0003t0009g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0003t0009g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0003t0009g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0003t0011g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0003t0030g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0003t0030g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0003t0031g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0003t0031g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0003t0035g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0003t0035g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0003t0060g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0003t0076g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0003t0077g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0003t0079g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0003t0081g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0003t0084g0283 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0003t0097g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0004t0003g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0004t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0004t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0004t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0004t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0004t0010g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0004t0021g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0004t0021g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0006t0002g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0006t0002g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0006t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0006t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0006t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0006t0020g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0007t0005g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0007t0006g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0007t0006g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0007t0064g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0008t0009g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0008t0009g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0008t0089g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0015t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0001c0018t0009g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0002c0002t0003g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0002c0002t0003g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0002c0002t0003g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0002c0002t0005g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0002c0002t0012g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0002c0002t0012g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0002c0002t0012g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0002c0002t0013g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0002c0002t0014g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0002c0002t0014g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0002c0002t0014g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0002c0002t0014g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0002c0002t0016g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0002c0002t0016g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0002c0002t0026g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0002c0002t0026g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0002c0002t0029g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0002c0002t0029g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0002c0002t0032g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0002c0002t0034g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0002c0002t0038g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0002c0002t0038g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0002c0002t0040g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0002c0002t0057g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0002c0002t0058g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0002c0002t0059g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0002c0002t0065g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0002c0002t0066g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0002c0002t0067g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0002c0002t0069g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0002c0002t0070g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0002c0002t0072g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0002c0002t0073g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0002c0002t0074g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0002c0002t0075g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0002c0002t0080g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0002c0002t0086g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0002c0002t0098g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0002c0009t0093g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0002c0009t0100g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0002c0013t0087g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0003c0005t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0003c0005t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0003c0005t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0003c0005t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0003c0005t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0003c0005t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0003c0005t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0003c0005t0004g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0004c0011t0007g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0005c0010t0043g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0005c0010t0043g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0006c0017t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0007c0016t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0008c0014t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
a0009c0012t0013g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00280 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | FIN | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG00280 | hp2 | a0001 | c0001 | t0017 | g0080 | EUR | FIN | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG00323 | hp1 | a0002 | c0002 | t0074 | g0265 | EUR | FIN | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG00323 | hp2 | a0001 | c0001 | t0003 | g0229 | EUR | FIN | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG00408 | hp2 | a0001 | c0001 | t0025 | g0074 | EAS | CHS | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | CHS | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | CHS | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG00438 | hp1 | a0002 | c0002 | t0016 | g0242 | EAS | CHS | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG00438 | hp2 | a0001 | c0004 | t0003 | g0104 | EAS | CHS | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG00544 | hp1 | a0001 | c0004 | t0021 | g0051 | EAS | CHS | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | CHS | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG00558 | hp2 | a0002 | c0002 | t0065 | g0244 | EAS | CHS | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | CHS | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG00621 | hp2 | a0001 | c0004 | t0003 | g0064 | EAS | CHS | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG00639 | hp1 | a0002 | c0002 | t0072 | g0241 | AMR | PUR | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | CHS | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | CHS | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG00733 | hp2 | a0001 | c0001 | t0088 | g0219 | AMR | PUR | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG00735 | hp1 | a0001 | c0001 | t0082 | g0289 | AMR | PUR | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG00738 | hp2 | a0001 | c0006 | t0002 | g0012 | AMR | PUR | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG00741 | hp1 | a0001 | c0001 | t0017 | g0063 | AMR | PUR | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG00741 | hp2 | a0003 | c0005 | t0001 | g0159 | AMR | PUR | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG01071 | hp2 | a0001 | c0001 | t0047 | g0166 | AMR | PUR | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG01074 | hp1 | a0001 | c0003 | t0035 | g0299 | AMR | PUR | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG01074 | hp2 | a0003 | c0005 | t0001 | g0016 | AMR | PUR | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG01081 | hp1 | a0002 | c0002 | t0066 | g0291 | AMR | PUR | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG01099 | hp1 | a0003 | c0005 | t0001 | g0162 | AMR | PUR | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG01099 | hp2 | a0001 | c0001 | t0023 | g0181 | AMR | PUR | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG01106 | hp1 | a0001 | c0001 | t0055 | g0116 | AMR | PUR | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG01109 | hp1 | a0002 | c0002 | t0040 | g0128 | AMR | PUR | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0055 | AMR | PUR | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG01167 | hp1 | a0001 | c0001 | t0005 | g0216 | AMR | PUR | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG01168 | hp1 | a0003 | c0005 | t0001 | g0167 | AMR | PUR | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG01169 | hp2 | a0003 | c0005 | t0001 | g0178 | AMR | PUR | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG01175 | hp1 | a0001 | c0003 | t0035 | g0297 | AMR | PUR | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG01175 | hp2 | a0001 | c0001 | t0099 | g0112 | AMR | PUR | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG01192 | hp1 | a0001 | c0003 | t0031 | g0300 | AMR | PUR | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG01192 | hp2 | a0001 | c0001 | t0049 | g0171 | AMR | PUR | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG01255 | hp2 | a0002 | c0002 | t0005 | g0261 | AMR | CLM | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG01256 | hp1 | a0001 | c0001 | t0018 | g0237 | AMR | CLM | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | CLM | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG01258 | hp1 | a0001 | c0001 | t0018 | g0236 | AMR | CLM | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG01361 | hp1 | a0001 | c0001 | t0061 | g0110 | AMR | CLM | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG01433 | hp1 | a0001 | c0001 | t0083 | g0264 | AMR | CLM | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG01433 | hp2 | a0001 | c0003 | t0009 | g0276 | AMR | CLM | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG01516 | hp1 | a0001 | c0001 | t0039 | g0218 | EUR | IBS | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0194 | EUR | IBS | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG01891 | hp1 | a0002 | c0002 | t0080 | g0270 | AFR | ACB | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG01891 | hp2 | a0001 | c0001 | t0007 | g0025 | AFR | ACB | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG01928 | hp1 | a0003 | c0005 | t0001 | g0016 | AMR | PEL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG01928 | hp2 | a0001 | c0006 | t0002 | g0035 | AMR | PEL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG01934 | hp1 | a0003 | c0005 | t0001 | g0168 | AMR | PEL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG01934 | hp2 | a0001 | c0006 | t0002 | g0008 | AMR | PEL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG01952 | hp1 | a0003 | c0005 | t0001 | g0169 | AMR | PEL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG01952 | hp2 | a0001 | c0003 | t0076 | g0280 | AMR | PEL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG01978 | hp1 | a0001 | c0003 | t0079 | g0296 | AMR | PEL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG01978 | hp2 | a0001 | c0006 | t0020 | g0111 | AMR | PEL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG01981 | hp1 | a0001 | c0001 | t0004 | g0145 | AMR | PEL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG01981 | hp2 | a0003 | c0005 | t0004 | g0175 | AMR | PEL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG01993 | hp1 | a0001 | c0003 | t0081 | g0268 | AMR | PEL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG01993 | hp2 | a0001 | c0006 | t0002 | g0049 | AMR | PEL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG02004 | hp2 | a0001 | c0006 | t0002 | g0012 | AMR | PEL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | KHV | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG02027 | hp2 | a0001 | c0008 | t0009 | g0275 | EAS | KHV | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG02040 | hp2 | a0001 | c0004 | t0021 | g0070 | EAS | KHV | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG02055 | hp1 | a0001 | c0007 | t0064 | g0294 | AFR | ACB | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG02056 | hp2 | a0001 | c0004 | t0003 | g0052 | EAS | KHV | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG02071 | hp2 | a0001 | c0001 | t0050 | g0193 | EAS | KHV | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | KHV | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | KHV | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | KHV | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG02080 | hp2 | a0001 | c0008 | t0089 | g0287 | EAS | KHV | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG02129 | hp1 | a0001 | c0008 | t0009 | g0094 | EAS | KHV | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG02129 | hp2 | a0002 | c0002 | t0069 | g0243 | EAS | KHV | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG02132 | hp2 | a0001 | c0004 | t0003 | g0053 | EAS | KHV | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG02145 | hp1 | a0001 | c0001 | t0006 | g0200 | AFR | ACB | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG02145 | hp2 | a0001 | c0001 | t0005 | g0214 | AFR | ACB | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | CDX | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | CDX | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG02257 | hp1 | a0002 | c0002 | t0014 | g0247 | AFR | ACB | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG02258 | hp1 | a0002 | c0002 | t0029 | g0269 | AFR | ACB | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG02258 | hp2 | a0001 | c0001 | t0053 | g0117 | AFR | ACB | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG02273 | hp1 | a0001 | c0003 | t0031 | g0298 | AMR | PEL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG02273 | hp2 | a0001 | c0001 | t0004 | g0138 | AMR | PEL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG02280 | hp1 | a0002 | c0002 | t0014 | g0250 | AFR | ACB | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG02280 | hp2 | a0001 | c0001 | t0011 | g0030 | AFR | ACB | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG02293 | hp2 | a0001 | c0006 | t0002 | g0008 | AMR | PEL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG02451 | hp1 | a0002 | c0002 | t0003 | g0251 | AFR | ACB | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG02451 | hp2 | a0001 | c0001 | t0006 | g0195 | AFR | ACB | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG02572 | hp1 | a0002 | c0002 | t0038 | g0302 | AFR | GWD | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG02572 | hp2 | a0001 | c0001 | t0056 | g0118 | AFR | GWD | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG02602 | hp2 | a0001 | c0001 | t0039 | g0217 | SAS | PJL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG02615 | hp1 | a0001 | c0003 | t0030 | g0274 | AFR | GWD | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG02615 | hp2 | a0001 | c0001 | t0011 | g0089 | AFR | GWD | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG02630 | hp1 | a0002 | c0002 | t0014 | g0248 | AFR | GWD | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG02630 | hp2 | a0002 | c0002 | t0038 | g0301 | AFR | GWD | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG02647 | hp1 | a0001 | c0001 | t0005 | g0033 | AFR | GWD | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG02647 | hp2 | a0001 | c0001 | t0002 | g0076 | AFR | GWD | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG02723 | hp1 | a0002 | c0002 | t0032 | g0021 | AFR | GWD | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG02723 | hp2 | a0001 | c0001 | t0068 | g0273 | AFR | GWD | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG02735 | hp1 | a0001 | c0001 | t0028 | g0066 | SAS | PJL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG02735 | hp2 | a0002 | c0002 | t0073 | g0240 | SAS | PJL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG02738 | hp1 | a0001 | c0001 | t0091 | g0098 | SAS | PJL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG02809 | hp1 | a0001 | c0001 | t0005 | g0215 | AFR | GWD | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG02809 | hp2 | a0002 | c0002 | t0032 | g0021 | AFR | GWD | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG02818 | hp1 | a0001 | c0003 | t0060 | g0278 | AFR | GWD | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG02818 | hp2 | a0001 | c0001 | t0015 | g0272 | AFR | GWD | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG02886 | hp1 | a0001 | c0001 | t0034 | g0024 | AFR | GWD | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG02886 | hp2 | a0001 | c0001 | t0019 | g0081 | AFR | GWD | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG02895 | hp1 | a0001 | c0001 | t0062 | g0031 | AFR | GWD | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG02895 | hp2 | a0002 | c0002 | t0003 | g0254 | AFR | GWD | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG02896 | hp1 | a0001 | c0001 | t0011 | g0114 | AFR | GWD | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG02896 | hp2 | a0004 | c0011 | t0007 | g0005 | AFR | GWD | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG02897 | hp1 | a0004 | c0011 | t0007 | g0005 | AFR | GWD | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG02897 | hp2 | a0002 | c0002 | t0003 | g0253 | AFR | GWD | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG02965 | hp1 | a0001 | c0001 | t0041 | g0113 | AFR | ESN | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG02965 | hp2 | a0001 | c0001 | t0015 | g0036 | AFR | ESN | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG02970 | hp1 | a0001 | c0001 | t0015 | g0037 | AFR | ESN | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG02970 | hp2 | a0001 | c0001 | t0027 | g0227 | AFR | ESN | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG02976 | hp1 | a0001 | c0001 | t0090 | g0075 | AFR | ESN | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG02976 | hp2 | a0002 | c0002 | t0029 | g0271 | AFR | ESN | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG03017 | hp1 | a0001 | c0001 | t0071 | g0091 | SAS | PJL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG03041 | hp1 | a0001 | c0007 | t0006 | g0198 | AFR | GWD | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG03041 | hp2 | a0001 | c0001 | t0054 | g0115 | AFR | GWD | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG03098 | hp1 | a0001 | c0001 | t0007 | g0101 | AFR | MSL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG03098 | hp2 | a0001 | c0001 | t0027 | g0226 | AFR | MSL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG03130 | hp1 | a0002 | c0002 | t0014 | g0249 | AFR | ESN | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG03130 | hp2 | a0001 | c0001 | t0011 | g0108 | AFR | ESN | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG03139 | hp1 | a0001 | c0001 | t0005 | g0034 | AFR | ESN | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG03139 | hp2 | a0001 | c0003 | t0077 | g0282 | AFR | ESN | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG03195 | hp1 | a0001 | c0001 | t0041 | g0082 | AFR | ESN | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG03195 | hp2 | a0001 | c0001 | t0022 | g0221 | AFR | ESN | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG03209 | hp1 | a0005 | c0010 | t0043 | g0224 | AFR | MSL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG03209 | hp2 | a0001 | c0003 | t0030 | g0279 | AFR | MSL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG03225 | hp1 | a0001 | c0001 | t0019 | g0059 | AFR | MSL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG03225 | hp2 | a0001 | c0007 | t0005 | g0231 | AFR | MSL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG03453 | hp1 | a0002 | c0002 | t0067 | g0290 | AFR | MSL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG03453 | hp2 | a0001 | c0001 | t0019 | g0097 | AFR | MSL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG03491 | hp1 | a0001 | c0001 | t0008 | g0160 | SAS | PJL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG03491 | hp2 | a0001 | c0001 | t0042 | g0054 | SAS | PJL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG03516 | hp1 | a0001 | c0001 | t0033 | g0023 | AFR | ESN | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG03516 | hp2 | a0001 | c0001 | t0006 | g0201 | AFR | ESN | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG03540 | hp1 | a0001 | c0001 | t0006 | g0196 | AFR | GWD | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG03540 | hp2 | a0001 | c0001 | t0037 | g0032 | AFR | GWD | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG03579 | hp1 | a0001 | c0001 | t0037 | g0090 | AFR | MSL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG03579 | hp2 | a0002 | c0002 | t0098 | g0235 | AFR | MSL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG03669 | hp1 | a0001 | c0001 | t0017 | g0079 | SAS | PJL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG03669 | hp2 | a0001 | c0001 | t0024 | g0188 | SAS | PJL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | STU | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | STU | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG03704 | hp1 | a0001 | c0001 | t0024 | g0202 | SAS | PJL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG03704 | hp2 | a0001 | c0001 | t0018 | g0092 | SAS | PJL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG03710 | hp1 | a0001 | c0001 | t0010 | g0060 | SAS | PJL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0007 | SAS | BEB | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | BEB | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG04115 | hp1 | a0002 | c0002 | t0086 | g0260 | SAS | STU | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | STU | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0103 | SAS | STU | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG04204 | hp2 | a0001 | c0001 | t0052 | g0152 | SAS | STU | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA18522 | hp1 | a0002 | c0002 | t0034 | g0292 | AFR | YRI | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA18522 | hp2 | a0002 | c0009 | t0100 | g0304 | AFR | YRI | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA18747 | hp1 | a0001 | c0001 | t0025 | g0040 | EAS | CHB | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | CHB | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA18906 | hp1 | a0001 | c0001 | t0007 | g0043 | AFR | YRI | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA18906 | hp2 | a0001 | c0001 | t0044 | g0222 | AFR | YRI | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA18939 | hp2 | a0001 | c0001 | t0036 | g0006 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA18941 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA18942 | hp1 | a0001 | c0001 | t0042 | g0065 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA18943 | hp1 | a0001 | c0003 | t0097 | g0284 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA18943 | hp2 | a0001 | c0001 | t0045 | g0058 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA18944 | hp1 | a0001 | c0001 | t0023 | g0140 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA18945 | hp2 | a0001 | c0003 | t0009 | g0281 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA18946 | hp1 | a0001 | c0001 | t0016 | g0228 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA18948 | hp1 | a0001 | c0001 | t0008 | g0134 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA18948 | hp2 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA18951 | hp1 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA18960 | hp1 | a0001 | c0001 | t0008 | g0133 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA18960 | hp2 | a0001 | c0001 | t0008 | g0210 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA18961 | hp1 | a0001 | c0001 | t0010 | g0086 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA18961 | hp2 | a0001 | c0001 | t0008 | g0165 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA18962 | hp2 | a0001 | c0001 | t0008 | g0163 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA18963 | hp2 | a0001 | c0001 | t0048 | g0027 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA18965 | hp1 | a0001 | c0015 | t0003 | g0099 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA18965 | hp2 | a0001 | c0003 | t0011 | g0277 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA18966 | hp1 | a0001 | c0001 | t0004 | g0179 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA18966 | hp2 | a0002 | c0002 | t0012 | g0266 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA18972 | hp1 | a0001 | c0001 | t0003 | g0044 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA18973 | hp2 | a0001 | c0001 | t0028 | g0085 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA18977 | hp1 | a0001 | c0001 | t0003 | g0067 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA18977 | hp2 | a0001 | c0001 | t0004 | g0174 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA18979 | hp2 | a0006 | c0017 | t0001 | g0205 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA18982 | hp1 | a0001 | c0018 | t0009 | g0285 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA18984 | hp1 | a0001 | c0001 | t0092 | g0046 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA18987 | hp1 | a0001 | c0001 | t0096 | g0057 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA18987 | hp2 | a0008 | c0014 | t0001 | g0122 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA18991 | hp1 | a0001 | c0001 | t0004 | g0147 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA18991 | hp2 | a0001 | c0001 | t0095 | g0084 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA18993 | hp2 | a0001 | c0001 | t0010 | g0050 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA18994 | hp1 | a0001 | c0001 | t0020 | g0083 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA18994 | hp2 | a0002 | c0002 | t0058 | g0259 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA18997 | hp1 | a0001 | c0001 | t0004 | g0131 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA18997 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA19000 | hp2 | a0001 | c0001 | t0004 | g0208 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA19003 | hp2 | a0002 | c0002 | t0026 | g0246 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA19006 | hp1 | a0002 | c0002 | t0012 | g0267 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA19009 | hp1 | a0001 | c0003 | t0009 | g0288 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA19010 | hp1 | a0001 | c0004 | t0010 | g0100 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA19011 | hp2 | a0001 | c0001 | t0021 | g0072 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA19030 | hp1 | a0001 | c0001 | t0022 | g0220 | AFR | LWK | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA19030 | hp2 | a0002 | c0013 | t0087 | g0293 | AFR | LWK | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA19043 | hp1 | a0001 | c0001 | t0006 | g0197 | AFR | LWK | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA19043 | hp2 | a0001 | c0001 | t0013 | g0029 | AFR | LWK | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA19054 | hp1 | a0001 | c0004 | t0003 | g0010 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA19063 | hp1 | a0001 | c0001 | t0004 | g0141 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA19063 | hp2 | a0001 | c0001 | t0003 | g0107 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA19064 | hp1 | a0001 | c0001 | t0012 | g0088 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA19064 | hp2 | a0002 | c0002 | t0016 | g0245 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA19065 | hp1 | a0002 | c0002 | t0070 | g0263 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA19065 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA19074 | hp1 | a0002 | c0002 | t0026 | g0258 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA19074 | hp2 | a0001 | c0001 | t0036 | g0006 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA19081 | hp2 | a0007 | c0016 | t0001 | g0146 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA19082 | hp1 | a0002 | c0002 | t0075 | g0262 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA19084 | hp2 | a0001 | c0006 | t0002 | g0105 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA19085 | hp2 | a0001 | c0001 | t0094 | g0056 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA19086 | hp1 | a0001 | c0001 | t0010 | g0230 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA19087 | hp1 | a0001 | c0001 | t0010 | g0087 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA19088 | hp2 | a0002 | c0002 | t0012 | g0255 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA19089 | hp1 | a0001 | c0004 | t0003 | g0010 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA19090 | hp2 | a0001 | c0001 | t0040 | g0071 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA19240 | hp1 | a0002 | c0002 | t0059 | g0252 | AFR | YRI | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA19240 | hp2 | a0002 | c0002 | t0057 | g0026 | AFR | YRI | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ASW | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA20129 | hp2 | a0001 | c0001 | t0020 | g0207 | AFR | ASW | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA20752 | hp1 | a0002 | c0002 | t0013 | g0257 | EUR | TSI | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA20752 | hp2 | a0001 | c0001 | t0003 | g0295 | EUR | TSI | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA20905 | hp2 | a0001 | c0001 | t0085 | g0077 | SAS | GIH | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG01123 | hp1 | a0001 | c0001 | t0033 | g0286 | AMR | CLM | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG01123 | hp2 | a0001 | c0001 | t0051 | g0156 | AMR | CLM | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG02486 | hp1 | a0002 | c0009 | t0093 | g0303 | AFR | ACB | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG02486 | hp2 | a0009 | c0012 | t0013 | g0256 | AFR | ACB | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | ACB | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG02559 | hp2 | a0001 | c0001 | t0007 | g0038 | AFR | ACB | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG03471 | hp1 | a0001 | c0001 | t0078 | g0135 | AFR | MSL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG03471 | hp2 | a0001 | c0001 | t0063 | g0039 | AFR | MSL | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG06807 | hp1 | a0005 | c0010 | t0043 | g0225 | AFR | USA | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
HG06807 | hp2 | a0001 | c0001 | t0007 | g0041 | AFR | USA | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA18955 | hp2 | a0001 | c0001 | t0046 | g0186 | EAS | JPT | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA20300 | hp1 | a0001 | c0007 | t0006 | g0199 | AFR | USA | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | USA | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | LWK | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
NA21309 | hp2 | a0001 | c0001 | t0013 | g0047 | AFR | LWK | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
homoSapiens_chm13v2 | hp1 | a0001 | c0003 | t0084 | g0283 | REF | REF | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0048 | REF | REF | TSC1_chr9_132886349_132949616 | TSC1 | chr9 | 132886349 | 132949616 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:132897540
|
G | C | 1 | a0008 | 1 | NA18987.hp2 | missense_variant | MODERATE | c.2696C>G | p.Thr899Ser | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 21/23 | 2913/8598 | 2696/3495 | 899/1164 | chr9 | 132897540 | ||
chr9:132905618
|
G | C | 1 | a0007 | 1 | NA19081.hp2 | missense_variant | MODERATE | c.1960C>G | p.Gln654Glu | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 15/23 | 2177/8598 | 1960/3495 | 654/1164 | chr9 | 132905618 | ||
chr9:132905818
|
T | C | 1 | a0003 | 9 | HG00741.hp2 HG01074.hp2 HG01099.hp1 others(6): Show |
missense_variant | MODERATE | c.1760A>G | p.Lys587Arg | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 15/23 | 1977/8598 | 1760/3495 | 587/1164 | chr9 | 132905818 | ||
chr9:132906827
|
G | A | 1 | a0005 | 2 | HG03209.hp1 HG06807.hp1 |
missense_variant | MODERATE | c.1342C>T | p.Pro448Ser | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 14/23 | 1559/8598 | 1342/3495 | 448/1164 | chr9 | 132906827 | ||
chr9:132910584
|
G | A | 1 | a0006 | 1 | NA18979.hp2 | missense_variant | MODERATE | c.1250C>T | p.Thr417Ile | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/23 | 1467/8598 | 1250/3495 | 417/1164 | chr9 | 132910584 | ||
chr9:132911517
|
A | G | 2 | a0002a0009 | 43 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(40): Show |
missense_variant | MODERATE | c.965T>C | p.Met322Thr | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 10/23 | 1182/8598 | 965/3495 | 322/1164 | chr9 | 132911517 | ||
chr9:132921430
|
T | A | 1 | a0004 | 2 | HG02896.hp2 HG02897.hp1 |
missense_variant | MODERATE | c.670A>T | p.Met224Leu | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/23 | 887/8598 | 670/3495 | 224/1164 | chr9 | 132921430 | ||
chr9:132925604
|
A | C | 1 | a0009 | 1 | HG02486.hp2 | missense_variant | MODERATE | c.346T>G | p.Leu116Val | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 5/23 | 563/8598 | 346/3495 | 116/1164 | chr9 | 132925604 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:132896406
|
G | A | 1 | a0001c0006 | 8 | HG00738.hp2 HG01928.hp2 HG01934.hp2 others(5): Show |
synonymous_variant | LOW | c.3324C>T | p.Gly1108Gly | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 3541/8598 | 3324/3495 | 1108/1164 | chr9 | 132896406 | ||
chr9:132896448
|
C | T | 2 | a0001c0007a0002c0009 | 6 | HG02055.hp1 HG02486.hp1 HG03041.hp1 others(3): Show |
synonymous_variant | LOW | c.3282G>A | p.Glu1094Glu | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 3499/8598 | 3282/3495 | 1094/1164 | chr9 | 132896448 | ||
chr9:132897330
|
G | A | 3 | a0001c0003a0001c0008a0001c0018 | 21 | HG01074.hp1 HG01175.hp1 HG01192.hp1 others(18): Show |
synonymous_variant | LOW | c.2829C>T | p.Ala943Ala | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 22/23 | 3046/8598 | 2829/3495 | 943/1164 | chr9 | 132897330 | ||
chr9:132904418
|
G | A | 1 | a0001c0015 | 1 | NA18965.hp1 | synonymous_variant | LOW | c.2034C>T | p.His678His | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 16/23 | 2251/8598 | 2034/3495 | 678/1164 | chr9 | 132904418 | ||
chr9:132905852
|
A | G | 1 | a0001c0004 | 9 | HG00438.hp2 HG00544.hp1 HG00621.hp2 others(6): Show |
synonymous_variant | LOW | c.1726T>C | p.Leu576Leu | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 15/23 | 1943/8598 | 1726/3495 | 576/1164 | chr9 | 132905852 | ||
chr9:132905877
|
C | T | 1 | a0002c0013 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.1701G>A | p.Ala567Ala | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 15/23 | 1918/8598 | 1701/3495 | 567/1164 | chr9 | 132905877 | ||
chr9:132906834
|
T | C | 4 | a0002c0002a0002c0009a0002c0013others(1): Show | 43 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(40): Show |
splice_region_variant&synonymous_variant | LOW | c.1335A>G | p.Glu445Glu | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 14/23 | 1552/8598 | 1335/3495 | 445/1164 | chr9 | 132906834 | ||
chr9:132921864
|
A | G | 1 | a0001c0008 | 3 | HG02027.hp2 HG02080.hp2 HG02129.hp1 |
synonymous_variant | LOW | c.618T>C | p.His206His | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 7/23 | 835/8598 | 618/3495 | 206/1164 | chr9 | 132921864 | ||
chr9:132925680
|
G | A | 1 | a0001c0018 | 1 | NA18982.hp1 | synonymous_variant | LOW | c.270C>T | p.Leu90Leu | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 5/23 | 487/8598 | 270/3495 | 90/1164 | chr9 | 132925680 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:132891472
|
A | G | 3 | a0001c0001t0019a0001c0001t0041a0001c0001t0090 | 6 | HG02886.hp2 HG02965.hp1 HG02976.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4763T>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 4763 | chr9 | 132891472 | |||||
chr9:132891637
|
C | T | 1 | a0001c0001t0049 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4598G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 4598 | chr9 | 132891637 | |||||
chr9:132891798
|
C | T | 28 | a0001c0001t0006a0001c0001t0012a0001c0001t0024others(25): Show | 44 | HG00735.hp1 HG01074.hp1 HG01081.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*4437G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 4437 | chr9 | 132891798 | |||||
chr9:132891981
|
C | T | 1 | a0001c0001t0048 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4254G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 4254 | chr9 | 132891981 | |||||
chr9:132892086
|
T | C | 1 | a0002c0002t0067 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4149A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 4149 | chr9 | 132892086 | |||||
chr9:132892178
|
C | T | 1 | a0001c0001t0068 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4057G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 4057 | chr9 | 132892178 | |||||
chr9:132892283
|
T | C | 1 | a0001c0001t0027 | 2 | HG02970.hp2 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3952A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 3952 | chr9 | 132892283 | |||||
chr9:132892356
|
C | A | 1 | a0001c0001t0050 | 1 | HG02071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3879G>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 3879 | chr9 | 132892356 | |||||
chr9:132892393
|
T | G | 1 | a0002c0002t0073 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3842A>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 3842 | chr9 | 132892393 | |||||
chr9:132892506
|
C | A | 2 | a0001c0003t0060a0005c0010t0043 | 3 | HG02818.hp1 HG03209.hp1 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3729G>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 3729 | chr9 | 132892506 | |||||
chr9:132892556
|
C | T | 85 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(82): Show | 237 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(234): Show |
3_prime_UTR_variant | MODIFIER | c.*3679G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 3679 | chr9 | 132892556 | |||||
chr9:132892669
|
C | T | 1 | a0001c0001t0023 | 2 | HG01099.hp2 NA18944.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3566G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 3566 | chr9 | 132892669 | |||||
chr9:132892697
|
T | C | 1 | a0001c0001t0056 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3538A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 3538 | chr9 | 132892697 | |||||
chr9:132893361
|
C | T | 1 | a0002c0002t0057 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2874G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 2874 | chr9 | 132893361 | |||||
chr9:132893363
|
C | T | 1 | a0001c0001t0047 | 1 | HG01071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2872G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 2872 | chr9 | 132893363 | |||||
chr9:132893502
|
T | C | 1 | a0002c0002t0057 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2733A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 2733 | chr9 | 132893502 | |||||
chr9:132893527
|
C | G | 2 | a0002c0002t0029a0002c0002t0080 | 3 | HG01891.hp1 HG02258.hp1 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2708G>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 2708 | chr9 | 132893527 | |||||
chr9:132893584
|
C | A | 2 | a0002c0002t0014a0002c0002t0074 | 5 | HG00323.hp1 HG02257.hp1 HG02280.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2651G>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 2651 | chr9 | 132893584 | |||||
chr9:132893607
|
C | G | 1 | a0001c0001t0088 | 1 | HG00733.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2628G>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 2628 | chr9 | 132893607 | |||||
chr9:132893677
|
T | C | 4 | a0001c0001t0022a0001c0001t0044a0001c0001t0054others(1): Show | 6 | HG02723.hp1 HG02809.hp2 HG03041.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2558A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 2558 | chr9 | 132893677 | |||||
chr9:132893717
|
C | T | 1 | a0001c0001t0036 | 2 | NA18939.hp2 NA19074.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2518G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 2518 | chr9 | 132893717 | |||||
chr9:132893774
|
C | T | 2 | a0002c0002t0057a0002c0013t0087 | 2 | NA19030.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2461G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 2461 | chr9 | 132893774 | |||||
chr9:132893798
|
C | T | 2 | a0002c0002t0066a0002c0002t0067 | 2 | HG01081.hp1 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2437G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 2437 | chr9 | 132893798 | |||||
chr9:132893817
|
C | T | 5 | a0001c0001t0053a0001c0001t0082a0001c0001t0083others(2): Show | 5 | HG00735.hp1 HG01081.hp1 HG01433.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2418G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 2418 | chr9 | 132893817 | |||||
chr9:132893881
|
T | C | 1 | a0002c0013t0087 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2354A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 2354 | chr9 | 132893881 | |||||
chr9:132894126
|
G | A | 1 | a0002c0002t0057 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2109C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 2109 | chr9 | 132894126 | |||||
chr9:132894301
|
T | C | 23 | a0001c0001t0006a0001c0001t0015a0001c0001t0016others(20): Show | 37 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*1934A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 1934 | chr9 | 132894301 | |||||
chr9:132894333
|
A | C | 1 | a0001c0007t0064 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1902T>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 1902 | chr9 | 132894333 | |||||
chr9:132894450
|
T | C | 2 | a0001c0001t0007a0004c0011t0007 | 7 | HG01891.hp2 HG02559.hp2 HG02896.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1785A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 1785 | chr9 | 132894450 | |||||
chr9:132894686
|
G | A | 1 | a0002c0002t0070 | 1 | NA19065.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1549C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 1549 | chr9 | 132894686 | |||||
chr9:132894693
|
T | TA | 25 | a0001c0001t0004a0001c0001t0007a0001c0001t0015others(22): Show | 42 | HG00438.hp1 HG00735.hp1 HG01081.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*1541dupT | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 1541 | chr9 | 132894693 | |||||
chr9:132894693
|
T | TAA | 6 | a0001c0001t0041a0001c0001t0083a0001c0001t0090others(3): Show | 7 | HG01433.hp1 HG01978.hp1 HG02486.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1540_*1541dupTT | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 1541 | chr9 | 132894693 | |||||
chr9:132894693
|
TA | T | 14 | a0001c0001t0008a0001c0001t0017a0001c0001t0018others(11): Show | 29 | HG00280.hp2 HG00741.hp1 HG01256.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*1541delT | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 1541 | chr9 | 132894693 | |||||
chr9:132894728
|
C | T | 92 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(89): Show | 250 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(247): Show |
3_prime_UTR_variant | MODIFIER | c.*1507G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 1507 | chr9 | 132894728 | |||||
chr9:132894747
|
G | A | 23 | a0001c0001t0001a0001c0001t0004a0001c0001t0008others(20): Show | 131 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(128): Show |
3_prime_UTR_variant | MODIFIER | c.*1488C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 1488 | chr9 | 132894747 | |||||
chr9:132894748
|
G | A | 7 | a0001c0001t0006a0001c0001t0015a0001c0001t0055others(4): Show | 14 | HG01081.hp1 HG01106.hp1 HG02145.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1487C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 1487 | chr9 | 132894748 | |||||
chr9:132894767
|
G | A | 1 | a0001c0001t0051 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1468C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 1468 | chr9 | 132894767 | |||||
chr9:132894783
|
T | G | 1 | a0001c0003t0084 | 1 | homoSapiens_chm13v2.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1452A>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 1452 | chr9 | 132894783 | |||||
chr9:132894863
|
A | C | 49 | a0001c0001t0005a0001c0001t0006a0001c0001t0015others(46): Show | 76 | HG00280.hp2 HG00558.hp2 HG00735.hp1 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*1372T>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 1372 | chr9 | 132894863 | |||||
chr9:132894913
|
G | A | 54 | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(51): Show | 174 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(171): Show |
3_prime_UTR_variant | MODIFIER | c.*1322C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 1322 | chr9 | 132894913 | |||||
chr9:132894960
|
A | C | 87 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(84): Show | 228 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(225): Show |
3_prime_UTR_variant | MODIFIER | c.*1275T>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 1275 | chr9 | 132894960 | |||||
chr9:132895183
|
C | T | 1 | a0002c0002t0058 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1052G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 1052 | chr9 | 132895183 | |||||
chr9:132895394
|
G | A | 2 | a0001c0001t0022a0001c0001t0044 | 3 | HG03195.hp2 NA18906.hp2 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*841C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 841 | chr9 | 132895394 | |||||
chr9:132895553
|
G | A | 7 | a0001c0001t0022a0001c0001t0044a0001c0001t0053others(4): Show | 9 | HG01106.hp1 HG02258.hp2 HG02572.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*682C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 682 | chr9 | 132895553 | |||||
chr9:132895736
|
G | A | 1 | a0001c0001t0052 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*499C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 499 | chr9 | 132895736 | |||||
chr9:132895830
|
T | C | 1 | a0001c0003t0097 | 1 | NA18943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*405A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 405 | chr9 | 132895830 | |||||
chr9:132895859
|
G | A | 7 | a0001c0001t0022a0001c0001t0044a0001c0001t0053others(4): Show | 9 | HG01106.hp1 HG02258.hp2 HG02572.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*376C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 376 | chr9 | 132895859 | |||||
chr9:132895939
|
G | C | 1 | a0002c0002t0098 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*296C>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 296 | chr9 | 132895939 | |||||
chr9:132895940
|
G | T | 1 | a0002c0002t0057 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*295C>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 295 | chr9 | 132895940 | |||||
chr9:132895945
|
GA | G | 25 | a0001c0001t0001a0001c0001t0004a0001c0001t0008others(22): Show | 134 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(131): Show |
3_prime_UTR_variant | MODIFIER | c.*289delT | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 289 | chr9 | 132895945 | |||||
chr9:132896030
|
C | T | 1 | a0001c0001t0045 | 1 | NA18943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*205G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 205 | chr9 | 132896030 | |||||
chr9:132896037
|
A | G | 2 | a0001c0001t0022a0001c0001t0044 | 3 | HG03195.hp2 NA18906.hp2 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*198T>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 23/23 | 198 | chr9 | 132896037 | |||||
chr9:132935051
|
G | A | 1 | a0005c0010t0043 | 2 | HG03209.hp1 HG06807.hp1 |
5_prime_UTR_variant | MODIFIER | c.-99C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/23 | 6179 | chr9 | 132935051 | |||||
chr9:132935081
|
T | A | 1 | a0001c0001t0099 | 1 | HG01175.hp2 | 5_prime_UTR_variant | MODIFIER | c.-129A>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/23 | 6209 | chr9 | 132935081 | |||||
chr9:132935082
|
G | C | 1 | a0002c0009t0100 | 1 | NA18522.hp2 | 5_prime_UTR_variant | MODIFIER | c.-130C>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/23 | 6210 | chr9 | 132935082 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:132896797
|
C | G | 9 | a0001c0001t0022g0220a0001c0001t0022g0221a0001c0001t0044g0222others(6): Show | 9 | HG01106.hp1 HG02258.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.2976-43G>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 22/22 | chr9 | 132896797 | ||||||
chr9:132896804
|
C | T | 1 | a0001c0001t0001g0126 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2976-50G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 22/22 | chr9 | 132896804 | ||||||
chr9:132896808
|
C | T | 3 | a0001c0001t0053g0117a0001c0001t0055g0116a0001c0001t0056g0118 | 3 | HG01106.hp1 HG02258.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.2976-54G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 22/22 | chr9 | 132896808 | ||||||
chr9:132897057
|
C | A | 5 | a0001c0001t0053g0117a0001c0001t0055g0116a0001c0001t0056g0118others(2): Show | 5 | HG01106.hp1 HG02258.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.2975+127G>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 22/22 | chr9 | 132897057 | ||||||
chr9:132897083
|
T | C | 9 | a0001c0001t0022g0220a0001c0001t0022g0221a0001c0001t0044g0222others(6): Show | 9 | HG01106.hp1 HG02258.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.2975+101A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 22/22 | chr9 | 132897083 | ||||||
chr9:132897372
|
T | C | 1 | a0001c0001t0002g0055 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2814-27A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 21/22 | chr9 | 132897372 | ||||||
chr9:132897613
|
G | GA | 9 | a0001c0001t0001g0132a0001c0001t0001g0150a0001c0001t0001g0154others(6): Show | 9 | HG01106.hp1 HG01167.hp2 NA18946.hp2 others(6): Show |
splice_region_variant&intron_variant | LOW | c.2626-4dupT | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 20/22 | chr9 | 132897613 | ||||||
chr9:132897613
|
G | GAA | 128 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(125): Show | 148 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(145): Show |
splice_region_variant&intron_variant | LOW | c.2626-5_2626-4dupTT | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 20/22 | chr9 | 132897613 | ||||||
chr9:132897613
|
GA | G | 11 | a0001c0001t0002g0073a0001c0001t0010g0050a0001c0001t0042g0054others(8): Show | 11 | HG01891.hp1 HG02015.hp1 HG02258.hp1 others(8): Show |
splice_region_variant&intron_variant | LOW | c.2626-4delT | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 20/22 | chr9 | 132897613 | ||||||
chr9:132897657
|
T | C | 1 | a0002c0013t0087g0293 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2626-47A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 20/22 | chr9 | 132897657 | ||||||
chr9:132897727
|
C | T | 50 | a0001c0001t0005g0033a0001c0001t0005g0034a0001c0001t0006g0195others(47): Show | 51 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.2626-117G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 20/22 | chr9 | 132897727 | ||||||
chr9:132897777
|
C | T | 31 | a0002c0002t0003g0251a0002c0002t0003g0253a0002c0002t0003g0254others(28): Show | 31 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.2626-167G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 20/22 | chr9 | 132897777 | ||||||
chr9:132897840
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2626-230C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 20/22 | chr9 | 132897840 | ||||||
chr9:132898021
|
ACAAT | A | 4 | a0001c0007t0005g0231a0001c0007t0064g0294a0002c0009t0093g0303others(1): Show | 4 | HG02055.hp1 HG02486.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2626-415_2626-412d others(6): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 20/22 | chr9 | 132898021 | ||||||
chr9:132898028
|
A | G | 1 | a0001c0001t0048g0027 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.2626-418T>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 20/22 | chr9 | 132898028 | ||||||
chr9:132898106
|
C | T | 4 | a0002c0002t0029g0269a0002c0002t0029g0271a0002c0002t0034g0292others(1): Show | 4 | HG01891.hp1 HG02258.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.2626-496G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 20/22 | chr9 | 132898106 | ||||||
chr9:132898184
|
A | G | 2 | a0001c0001t0027g0226a0001c0001t0027g0227 | 2 | HG02970.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2626-574T>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 20/22 | chr9 | 132898184 | ||||||
chr9:132898411
|
T | C | 1 | a0001c0001t0085g0077 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2626-801A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 20/22 | chr9 | 132898411 | ||||||
chr9:132898419
|
T | C | 2 | a0001c0001t0082g0289a0001c0001t0083g0264 | 2 | HG00735.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.2626-809A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 20/22 | chr9 | 132898419 | ||||||
chr9:132898453
|
C | G | 1 | a0001c0004t0003g0052 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2626-843G>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 20/22 | chr9 | 132898453 | ||||||
chr9:132898672
|
T | C | 103 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(100): Show | 124 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.2626-1062A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 20/22 | chr9 | 132898672 | ||||||
chr9:132898673
|
G | A | 1 | a0001c0001t0001g0185 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.2626-1063C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 20/22 | chr9 | 132898673 | ||||||
chr9:132898777
|
T | C | 61 | a0001c0001t0001g0017a0001c0001t0005g0033a0001c0001t0005g0034others(58): Show | 63 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.2626-1167A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 20/22 | chr9 | 132898777 | ||||||
chr9:132898969
|
C | T | 20 | a0001c0001t0005g0033a0001c0001t0005g0034a0001c0001t0006g0195others(17): Show | 21 | HG01081.hp1 HG01891.hp1 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.2626-1359G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 20/22 | chr9 | 132898969 | ||||||
chr9:132898970
|
G | A | 1 | a0002c0002t0057g0026 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2626-1360C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 20/22 | chr9 | 132898970 | ||||||
chr9:132899149
|
T | A | 54 | a0001c0001t0005g0033a0001c0001t0005g0034a0001c0001t0006g0195others(51): Show | 55 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.2626-1539A>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 20/22 | chr9 | 132899149 | ||||||
chr9:132899184
|
C | A | 3 | a0001c0001t0053g0117a0001c0001t0056g0118a0002c0002t0057g0026 | 3 | HG02258.hp2 HG02572.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2625+1531G>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 20/22 | chr9 | 132899184 | ||||||
chr9:132899218
|
G | A | 1 | a0001c0001t0001g0203 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2625+1497C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 20/22 | chr9 | 132899218 | ||||||
chr9:132899301
|
C | T | 1 | a0002c0002t0003g0251 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2625+1414G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 20/22 | chr9 | 132899301 | ||||||
chr9:132899330
|
A | G | 1 | a0001c0001t0078g0135 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2625+1385T>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 20/22 | chr9 | 132899330 | ||||||
chr9:132899361
|
T | C | 53 | a0001c0001t0005g0033a0001c0001t0005g0034a0001c0001t0006g0195others(50): Show | 54 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.2625+1354A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 20/22 | chr9 | 132899361 | ||||||
chr9:132899454
|
C | T | 1 | a0001c0001t0001g0164 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2625+1261G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 20/22 | chr9 | 132899454 | ||||||
chr9:132899816
|
C | A | 167 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(164): Show | 189 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.2625+899G>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 20/22 | chr9 | 132899816 | ||||||
chr9:132900040
|
A | C | 53 | a0001c0001t0005g0033a0001c0001t0005g0034a0001c0001t0006g0195others(50): Show | 54 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.2625+675T>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 20/22 | chr9 | 132900040 | ||||||
chr9:132900051
|
T | C | 2 | a0005c0010t0043g0224a0005c0010t0043g0225 | 2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2625+664A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 20/22 | chr9 | 132900051 | ||||||
chr9:132900143
|
T | C | 53 | a0001c0001t0005g0033a0001c0001t0005g0034a0001c0001t0006g0195others(50): Show | 54 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.2625+572A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 20/22 | chr9 | 132900143 | ||||||
chr9:132900168
|
C | T | 1 | a0002c0002t0086g0260 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2625+547G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 20/22 | chr9 | 132900168 | ||||||
chr9:132900234
|
G | A | 1 | a0001c0001t0033g0286 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2625+481C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 20/22 | chr9 | 132900234 | ||||||
chr9:132900323
|
A | G | 1 | a0002c0002t0072g0241 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2625+392T>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 20/22 | chr9 | 132900323 | ||||||
chr9:132900331
|
G | GA | 53 | a0001c0001t0005g0033a0001c0001t0005g0034a0001c0001t0006g0195others(50): Show | 54 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.2625+383dupT | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 20/22 | chr9 | 132900331 | ||||||
chr9:132900530
|
T | C | 1 | a0002c0002t0098g0235 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2625+185A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 20/22 | chr9 | 132900530 | ||||||
chr9:132900640
|
T | A | 4 | a0002c0002t0029g0269a0002c0002t0029g0271a0002c0002t0034g0292others(1): Show | 4 | HG01891.hp1 HG02258.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.2625+75A>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 20/22 | chr9 | 132900640 | ||||||
chr9:132900647
|
C | T | 102 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(99): Show | 123 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.2625+68G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 20/22 | chr9 | 132900647 | ||||||
chr9:132900890
|
A | G | 2 | a0003c0005t0001g0167a0003c0005t0001g0178 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2503-53T>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 19/22 | chr9 | 132900890 | ||||||
chr9:132900954
|
C | A | 53 | a0001c0001t0005g0033a0001c0001t0005g0034a0001c0001t0006g0195others(50): Show | 54 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.2503-117G>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 19/22 | chr9 | 132900954 | ||||||
chr9:132900980
|
C | T | 1 | a0001c0007t0005g0231 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2503-143G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 19/22 | chr9 | 132900980 | ||||||
chr9:132901066
|
G | A | 7 | a0001c0003t0009g0281a0001c0003t0009g0288a0001c0003t0011g0277others(4): Show | 7 | HG02027.hp2 HG02080.hp2 HG02129.hp1 others(4): Show |
intron_variant | MODIFIER | c.2503-229C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 19/22 | chr9 | 132901066 | ||||||
chr9:132901169
|
C | T | 2 | a0001c0007t0005g0231a0001c0007t0064g0294 | 2 | HG02055.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2503-332G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 19/22 | chr9 | 132901169 | ||||||
chr9:132901225
|
G | A | 1 | a0001c0001t0023g0140 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2502+364C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 19/22 | chr9 | 132901225 | ||||||
chr9:132901458
|
G | A | 30 | a0002c0002t0003g0251a0002c0002t0003g0253a0002c0002t0003g0254others(27): Show | 30 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.2502+131C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 19/22 | chr9 | 132901458 | ||||||
chr9:132901538
|
T | C | 34 | a0001c0001t0002g0238a0001c0001t0003g0002a0001c0001t0003g0028others(31): Show | 38 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.2502+51A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 19/22 | chr9 | 132901538 | ||||||
chr9:132901734
|
A | G | 53 | a0001c0001t0005g0033a0001c0001t0005g0034a0001c0001t0006g0195others(50): Show | 54 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.2392-35T>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 18/22 | chr9 | 132901734 | ||||||
chr9:132901882
|
A | G | 7 | a0001c0003t0009g0281a0001c0003t0009g0288a0001c0003t0011g0277others(4): Show | 7 | HG02027.hp2 HG02080.hp2 HG02129.hp1 others(4): Show |
intron_variant | MODIFIER | c.2392-183T>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 18/22 | chr9 | 132901882 | ||||||
chr9:132901921
|
G | A | 1 | a0001c0001t0099g0112 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2392-222C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 18/22 | chr9 | 132901921 | ||||||
chr9:132902009
|
G | A | 2 | a0001c0001t0001g0130a0001c0001t0008g0134 | 2 | NA18948.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.2392-310C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 18/22 | chr9 | 132902009 | ||||||
chr9:132902064
|
T | C | 53 | a0001c0001t0005g0033a0001c0001t0005g0034a0001c0001t0006g0195others(50): Show | 54 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.2392-365A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 18/22 | chr9 | 132902064 | ||||||
chr9:132902241
|
T | C | 1 | a0001c0007t0005g0231 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2391+364A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 18/22 | chr9 | 132902241 | ||||||
chr9:132902324
|
T | A | 14 | a0001c0001t0002g0009a0001c0001t0002g0042a0001c0001t0002g0061others(11): Show | 15 | HG00408.hp2 HG00423.hp1 HG00673.hp1 others(12): Show |
intron_variant | MODIFIER | c.2391+281A>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 18/22 | chr9 | 132902324 | ||||||
chr9:132902406
|
T | C | 1 | a0001c0001t0002g0069 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2391+199A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 18/22 | chr9 | 132902406 | ||||||
chr9:132902451
|
T | C | 2 | a0002c0009t0093g0303a0002c0009t0100g0304 | 2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2391+154A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 18/22 | chr9 | 132902451 | ||||||
chr9:132902571
|
C | T | 5 | a0001c0001t0033g0023a0001c0001t0033g0286a0001c0001t0034g0024others(2): Show | 5 | HG00735.hp1 HG01123.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.2391+34G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 18/22 | chr9 | 132902571 | ||||||
chr9:132903130
|
G | A | 2 | a0002c0009t0093g0303a0002c0009t0100g0304 | 2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2209-343C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 17/22 | chr9 | 132903130 | ||||||
chr9:132903257
|
T | C | 1 | a0002c0002t0034g0292 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2208+394A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 17/22 | chr9 | 132903257 | ||||||
chr9:132903318
|
G | A | 2 | a0005c0010t0043g0224a0005c0010t0043g0225 | 2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2208+333C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 17/22 | chr9 | 132903318 | ||||||
chr9:132903440
|
C | T | 30 | a0002c0002t0003g0251a0002c0002t0003g0253a0002c0002t0003g0254others(27): Show | 30 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.2208+211G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 17/22 | chr9 | 132903440 | ||||||
chr9:132903480
|
T | C | 4 | a0001c0001t0001g0019a0001c0001t0001g0194a0001c0001t0001g0206others(1): Show | 5 | HG00280.hp1 HG01071.hp2 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.2208+171A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 17/22 | chr9 | 132903480 | ||||||
chr9:132903559
|
T | C | 1 | a0001c0006t0002g0049 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.2208+92A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 17/22 | chr9 | 132903559 | ||||||
chr9:132904143
|
T | C | 53 | a0001c0001t0005g0033a0001c0001t0005g0034a0001c0001t0006g0195others(50): Show | 54 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.2041+268A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 16/22 | chr9 | 132904143 | ||||||
chr9:132904147
|
T | A | 1 | a0001c0001t0078g0135 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2041+264A>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 16/22 | chr9 | 132904147 | ||||||
chr9:132904294
|
G | A | 1 | a0001c0001t0090g0075 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2041+117C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 16/22 | chr9 | 132904294 | ||||||
chr9:132904619
|
TACACTGG | T | 42 | a0002c0002t0003g0251a0002c0002t0003g0253a0002c0002t0003g0254others(39): Show | 43 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.1998-172_1998-166d others(9): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 15/22 | chr9 | 132904619 | ||||||
chr9:132904637
|
A | C | 1 | a0001c0001t0001g0120 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1998-183T>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 15/22 | chr9 | 132904637 | ||||||
chr9:132904756
|
G | A | 1 | a0001c0001t0039g0218 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1998-302C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 15/22 | chr9 | 132904756 | ||||||
chr9:132904836
|
C | A | 1 | a0001c0001t0002g0069 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1998-382G>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 15/22 | chr9 | 132904836 | ||||||
chr9:132904901
|
A | G | 302 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(299): Show | 334 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(331): Show |
intron_variant | MODIFIER | c.1998-447T>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 15/22 | chr9 | 132904901 | ||||||
chr9:132904981
|
T | C | 1 | a0001c0001t0003g0045 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1998-527A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 15/22 | chr9 | 132904981 | ||||||
chr9:132905183
|
A | AAAT | 42 | a0002c0002t0003g0251a0002c0002t0003g0253a0002c0002t0003g0254others(39): Show | 43 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.1997+395_1997+397d others(5): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 15/22 | chr9 | 132905183 | ||||||
chr9:132905425
|
A | G | 1 | a0001c0001t0055g0116 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1997+156T>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 15/22 | chr9 | 132905425 | ||||||
chr9:132905448
|
T | C | 2 | a0001c0001t0027g0226a0001c0001t0027g0227 | 2 | HG02970.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1997+133A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 15/22 | chr9 | 132905448 | ||||||
chr9:132906176
|
G | A | 42 | a0002c0002t0003g0251a0002c0002t0003g0253a0002c0002t0003g0254others(39): Show | 43 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.1439-37C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 14/22 | chr9 | 132906176 | ||||||
chr9:132906263
|
C | T | 1 | a0002c0013t0087g0293 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1439-124G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 14/22 | chr9 | 132906263 | ||||||
chr9:132906322
|
G | C | 42 | a0002c0002t0003g0251a0002c0002t0003g0253a0002c0002t0003g0254others(39): Show | 43 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.1439-183C>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 14/22 | chr9 | 132906322 | ||||||
chr9:132906348
|
C | G | 26 | a0001c0001t0033g0023a0001c0001t0033g0286a0001c0001t0034g0024others(23): Show | 26 | HG00735.hp1 HG01074.hp1 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.1439-209G>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 14/22 | chr9 | 132906348 | ||||||
chr9:132906461
|
A | G | 3 | a0001c0001t0053g0117a0001c0001t0055g0116a0001c0001t0056g0118 | 3 | HG01106.hp1 HG02258.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1438+270T>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 14/22 | chr9 | 132906461 | ||||||
chr9:132906548
|
C | CA | 20 | a0001c0001t0001g0125a0001c0001t0001g0170a0001c0001t0001g0234others(17): Show | 20 | HG00733.hp2 HG01192.hp1 HG01192.hp2 others(17): Show |
intron_variant | MODIFIER | c.1438+182dupT | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 14/22 | chr9 | 132906548 | ||||||
chr9:132906548
|
CA | C | 37 | a0001c0001t0002g0068a0001c0001t0002g0069a0001c0001t0028g0066others(34): Show | 38 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.1438+182delT | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 14/22 | chr9 | 132906548 | ||||||
chr9:132906590
|
A | G | 1 | a0001c0001t0078g0135 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1438+141T>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 14/22 | chr9 | 132906590 | ||||||
chr9:132906639
|
C | A | 42 | a0002c0002t0003g0251a0002c0002t0003g0253a0002c0002t0003g0254others(39): Show | 43 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.1438+92G>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 14/22 | chr9 | 132906639 | ||||||
chr9:132906890
|
G | C | 30 | a0002c0002t0003g0251a0002c0002t0003g0253a0002c0002t0003g0254others(27): Show | 30 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.1334-55C>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 13/22 | chr9 | 132906890 | ||||||
chr9:132907037
|
T | C | 1 | a0001c0001t0001g0149 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1334-202A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 13/22 | chr9 | 132907037 | ||||||
chr9:132907092
|
G | A | 42 | a0002c0002t0003g0251a0002c0002t0003g0253a0002c0002t0003g0254others(39): Show | 43 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.1333+209C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 13/22 | chr9 | 132907092 | ||||||
chr9:132907114
|
T | C | 5 | a0001c0001t0033g0023a0001c0001t0033g0286a0001c0001t0034g0024others(2): Show | 5 | HG00735.hp1 HG01123.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.1333+187A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 13/22 | chr9 | 132907114 | ||||||
chr9:132907382
|
A | G | 1 | a0001c0001t0001g0233 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1264-12T>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132907382 | ||||||
chr9:132907520
|
G | A | 1 | a0002c0002t0057g0026 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1264-150C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132907520 | ||||||
chr9:132907543
|
G | A | 1 | a0001c0001t0001g0233 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1264-173C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132907543 | ||||||
chr9:132907560
|
G | GC | 42 | a0002c0002t0003g0251a0002c0002t0003g0253a0002c0002t0003g0254others(39): Show | 43 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.1264-191dupG | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132907560 | ||||||
chr9:132907581
|
C | T | 30 | a0002c0002t0003g0251a0002c0002t0003g0253a0002c0002t0003g0254others(27): Show | 30 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.1264-211G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132907581 | ||||||
chr9:132907663
|
T | C | 2 | a0001c0001t0001g0143a0001c0001t0048g0027 | 2 | NA18963.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.1264-293A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132907663 | ||||||
chr9:132907765
|
C | T | 9 | a0001c0001t0001g0121a0001c0001t0001g0182a0001c0001t0001g0183others(6): Show | 9 | HG02015.hp2 HG02071.hp1 NA18942.hp2 others(6): Show |
intron_variant | MODIFIER | c.1264-395G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132907765 | ||||||
chr9:132907807
|
C | A | 2 | a0001c0001t0027g0226a0001c0001t0027g0227 | 2 | HG02970.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1264-437G>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132907807 | ||||||
chr9:132907813
|
G | A | 2 | a0001c0001t0002g0042a0001c0001t0002g0078 | 2 | NA18980.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.1264-443C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132907813 | ||||||
chr9:132907918
|
C | A | 42 | a0002c0002t0003g0251a0002c0002t0003g0253a0002c0002t0003g0254others(39): Show | 43 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.1264-548G>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132907918 | ||||||
chr9:132908052
|
A | G | 1 | a0001c0001t0001g0234 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1264-682T>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132908052 | ||||||
chr9:132908137
|
T | TTTTG | 42 | a0002c0002t0003g0251a0002c0002t0003g0253a0002c0002t0003g0254others(39): Show | 43 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.1264-768_1264-767i others(6): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132908137 | ||||||
chr9:132908262
|
C | T | 42 | a0002c0002t0003g0251a0002c0002t0003g0253a0002c0002t0003g0254others(39): Show | 43 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.1264-892G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132908262 | ||||||
chr9:132908327
|
A | G | 42 | a0002c0002t0003g0251a0002c0002t0003g0253a0002c0002t0003g0254others(39): Show | 43 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.1264-957T>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132908327 | ||||||
chr9:132908367
|
G | A | 42 | a0002c0002t0003g0251a0002c0002t0003g0253a0002c0002t0003g0254others(39): Show | 43 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.1264-997C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132908367 | ||||||
chr9:132908375
|
C | T | 2 | a0001c0001t0004g0147a0001c0001t0004g0179 | 2 | NA18966.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.1264-1005G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132908375 | ||||||
chr9:132908607
|
A | C | 1 | a0001c0001t0018g0092 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1264-1237T>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132908607 | ||||||
chr9:132908695
|
C | T | 1 | a0001c0001t0063g0039 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1264-1325G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132908695 | ||||||
chr9:132908782
|
A | C | 114 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(111): Show | 135 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.1264-1412T>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132908782 | ||||||
chr9:132908864
|
G | A | 2 | a0002c0009t0093g0303a0002c0009t0100g0304 | 2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1264-1494C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132908864 | ||||||
chr9:132908901
|
C | CT | 8 | a0001c0001t0001g0126a0001c0001t0001g0157a0001c0001t0001g0191others(5): Show | 8 | HG00544.hp1 HG02145.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.1264-1532dupA | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132908901 | ||||||
chr9:132908901
|
C | CTTTTTTT others(3): Show |
2 | a0002c0009t0093g0303a0002c0009t0100g0304 | 2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1264-1541_1264-153 others(14): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132908901 | ||||||
chr9:132908901
|
C | CTTTTTTT others(5): Show |
2 | a0002c0002t0013g0257a0009c0012t0013g0256 | 2 | HG02486.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1264-1543_1264-153 others(16): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132908901 | ||||||
chr9:132908901
|
C | CTTTTTTT others(6): Show |
1 | a0002c0002t0005g0261 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1264-1544_1264-153 others(17): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132908901 | ||||||
chr9:132908901
|
C | CTTTTTTT others(8): Show |
1 | a0002c0002t0066g0291 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1264-1546_1264-153 others(19): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132908901 | ||||||
chr9:132908901
|
C | CTTTTTTT others(9): Show |
1 | a0002c0002t0067g0290 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1264-1547_1264-153 others(20): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132908901 | ||||||
chr9:132908901
|
C | CTTTTTTT others(10): Show |
1 | a0001c0001t0027g0226 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1264-1548_1264-153 others(21): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132908901 | ||||||
chr9:132908901
|
C | CTTTTTTT others(11): Show |
1 | a0002c0002t0098g0235 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1264-1532_1264-153 others(22): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132908901 | ||||||
chr9:132908901
|
C | CTTTTTTT others(12): Show |
2 | a0001c0001t0027g0227a0002c0002t0057g0026 | 2 | HG02970.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1264-1532_1264-153 others(23): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132908901 | ||||||
chr9:132908901
|
C | CTTTTTTT others(14): Show |
1 | a0002c0002t0032g0021 | 2 | HG02723.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1264-1532_1264-153 others(25): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132908901 | ||||||
chr9:132908901
|
C | CTTTTTTT others(16): Show |
4 | a0002c0002t0003g0251a0002c0002t0012g0266a0002c0002t0012g0267others(1): Show | 4 | HG02451.hp1 NA18966.hp2 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.1264-1532_1264-153 others(27): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132908901 | ||||||
chr9:132908901
|
C | CTTTTTTT others(17): Show |
4 | a0002c0002t0016g0245a0002c0002t0059g0252a0002c0002t0075g0262others(1): Show | 4 | HG04115.hp1 NA19064.hp2 NA19082.hp1 others(1): Show |
intron_variant | MODIFIER | c.1264-1532_1264-153 others(28): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132908901 | ||||||
chr9:132908901
|
C | CTTTTTTT others(18): Show |
3 | a0002c0002t0016g0242a0002c0002t0026g0246a0002c0002t0065g0244 | 3 | HG00438.hp1 HG00558.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1264-1532_1264-153 others(29): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132908901 | ||||||
chr9:132908901
|
C | CTTTTTTT others(19): Show |
2 | a0002c0002t0040g0128a0002c0002t0069g0243 | 2 | HG01109.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.1264-1532_1264-153 others(30): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132908901 | ||||||
chr9:132908901
|
C | CTTTTTTT others(20): Show |
2 | a0002c0002t0073g0240a0005c0010t0043g0225 | 2 | HG02735.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1264-1532_1264-153 others(31): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132908901 | ||||||
chr9:132908901
|
C | CTTTTTTT others(21): Show |
3 | a0002c0002t0003g0254a0002c0002t0058g0259a0005c0010t0043g0224 | 3 | HG02895.hp2 HG03209.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.1264-1532_1264-153 others(32): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132908901 | ||||||
chr9:132908901
|
C | CTTTTTTT others(22): Show |
2 | a0002c0002t0003g0253a0002c0002t0014g0249 | 2 | HG02897.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1264-1532_1264-153 others(33): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132908901 | ||||||
chr9:132908901
|
C | CTTTTTTT others(23): Show |
4 | a0002c0002t0012g0255a0002c0002t0014g0247a0002c0002t0014g0248others(1): Show | 4 | HG00323.hp1 HG02257.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1264-1532_1264-153 others(34): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132908901 | ||||||
chr9:132908901
|
C | CTTTTTTT others(24): Show |
1 | a0002c0002t0038g0302 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1264-1532_1264-153 others(35): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132908901 | ||||||
chr9:132908901
|
C | CTTTTTTT others(25): Show |
1 | a0002c0002t0038g0301 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1264-1532_1264-153 others(36): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132908901 | ||||||
chr9:132908901
|
C | CTTTTTTT others(26): Show |
1 | a0002c0002t0014g0250 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1264-1532_1264-153 others(37): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132908901 | ||||||
chr9:132909193
|
C | T | 1 | a0002c0002t0014g0248 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1263+1378G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132909193 | ||||||
chr9:132909248
|
C | T | 2 | a0001c0001t0010g0050a0001c0001t0010g0086 | 2 | NA18961.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.1263+1323G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132909248 | ||||||
chr9:132909473
|
T | C | 2 | a0001c0001t0017g0063a0001c0001t0017g0079 | 2 | HG00741.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.1263+1098A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132909473 | ||||||
chr9:132910136
|
C | CA | 7 | a0001c0001t0001g0170a0001c0001t0002g0061a0001c0006t0002g0105others(4): Show | 7 | HG03209.hp1 HG06807.hp1 NA18981.hp1 others(4): Show |
intron_variant | MODIFIER | c.1263+434dupT | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132910136 | ||||||
chr9:132910179
|
T | C | 30 | a0002c0002t0003g0251a0002c0002t0003g0253a0002c0002t0003g0254others(27): Show | 30 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.1263+392A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132910179 | ||||||
chr9:132910256
|
G | A | 4 | a0002c0002t0032g0021a0002c0002t0066g0291a0002c0002t0067g0290others(1): Show | 5 | HG01081.hp1 HG02723.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1263+315C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132910256 | ||||||
chr9:132910265
|
C | T | 2 | a0001c0001t0015g0036a0001c0001t0015g0037 | 2 | HG02965.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1263+306G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132910265 | ||||||
chr9:132910301
|
C | CA | 24 | a0001c0001t0001g0125a0001c0001t0001g0150a0001c0001t0001g0158others(21): Show | 24 | HG00621.hp2 HG00673.hp2 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.1263+269dupT | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132910301 | ||||||
chr9:132910301
|
CA | C | 39 | a0001c0001t0001g0148a0001c0001t0042g0065a0002c0002t0003g0251others(36): Show | 40 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.1263+269delT | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132910301 | ||||||
chr9:132910465
|
C | T | 4 | a0001c0001t0011g0089a0001c0001t0011g0108a0001c0001t0011g0114others(1): Show | 4 | HG02615.hp2 HG02896.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1263+106G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 12/22 | chr9 | 132910465 | ||||||
chr9:132910725
|
T | C | 42 | a0002c0002t0003g0251a0002c0002t0003g0253a0002c0002t0003g0254others(39): Show | 43 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.1142-33A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 11/22 | chr9 | 132910725 | ||||||
chr9:132910939
|
C | T | 4 | a0001c0001t0022g0220a0001c0001t0022g0221a0001c0001t0044g0222others(1): Show | 4 | HG03041.hp2 HG03195.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1141+63G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 11/22 | chr9 | 132910939 | ||||||
chr9:132911187
|
A | G | 2 | a0001c0001t0001g0017a0001c0001t0049g0171 | 3 | HG00733.hp1 HG01192.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1030-74T>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 10/22 | chr9 | 132911187 | ||||||
chr9:132911625
|
T | TA | 6 | a0001c0001t0001g0158a0001c0001t0002g0061a0001c0001t0082g0289others(3): Show | 6 | HG00735.hp1 HG01175.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.914-58dupT | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 9/22 | chr9 | 132911625 | ||||||
chr9:132911625
|
TA | T | 174 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0013others(171): Show | 202 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.914-58delT | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 9/22 | chr9 | 132911625 | ||||||
chr9:132911625
|
TAA | T | 39 | a0001c0001t0001g0123a0001c0001t0001g0137a0001c0001t0001g0150others(36): Show | 40 | HG00733.hp2 HG01099.hp1 HG01099.hp2 others(37): Show |
intron_variant | MODIFIER | c.914-59_914-58delTT | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 9/22 | chr9 | 132911625 | ||||||
chr9:132911625
|
TAAAAA | T | 6 | a0002c0002t0029g0269a0002c0002t0029g0271a0002c0002t0032g0021others(3): Show | 7 | HG01891.hp1 HG02258.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.914-62_914-58delTT others(3): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 9/22 | chr9 | 132911625 | ||||||
chr9:132911625
|
TAAAAAA | T | 30 | a0002c0002t0003g0253a0002c0002t0003g0254a0002c0002t0005g0261others(27): Show | 30 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.914-63_914-58delTT others(4): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 9/22 | chr9 | 132911625 | ||||||
chr9:132911625
|
TAAAAAAA others(5): Show |
T | 1 | a0001c0001t0054g0115 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.914-69_914-58delTT others(10): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 9/22 | chr9 | 132911625 | ||||||
chr9:132911625
|
TAAAAAAA others(10): Show |
T | 1 | a0002c0002t0057g0026 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.914-74_914-58delTT others(15): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 9/22 | chr9 | 132911625 | ||||||
chr9:132911769
|
C | G | 4 | a0001c0001t0022g0220a0001c0001t0022g0221a0001c0001t0044g0222others(1): Show | 4 | HG03041.hp2 HG03195.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.914-201G>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 9/22 | chr9 | 132911769 | ||||||
chr9:132911912
|
C | T | 1 | a0001c0001t0001g0161 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.914-344G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 9/22 | chr9 | 132911912 | ||||||
chr9:132911926
|
T | C | 1 | a0001c0001t0012g0088 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.913+356A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 9/22 | chr9 | 132911926 | ||||||
chr9:132911927
|
G | C | 1 | a0001c0001t0001g0191 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.913+355C>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 9/22 | chr9 | 132911927 | ||||||
chr9:132912094
|
C | T | 1 | a0001c0007t0005g0231 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.913+188G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 9/22 | chr9 | 132912094 | ||||||
chr9:132912840
|
G | A | 30 | a0002c0002t0003g0251a0002c0002t0003g0253a0002c0002t0003g0254others(27): Show | 30 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.738-383C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132912840 | ||||||
chr9:132912885
|
G | A | 42 | a0002c0002t0003g0251a0002c0002t0003g0253a0002c0002t0003g0254others(39): Show | 43 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.738-428C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132912885 | ||||||
chr9:132912900
|
T | C | 41 | a0002c0002t0003g0251a0002c0002t0003g0253a0002c0002t0003g0254others(38): Show | 42 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.738-443A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132912900 | ||||||
chr9:132913006
|
C | T | 26 | a0001c0001t0033g0023a0001c0001t0033g0286a0001c0001t0034g0024others(23): Show | 26 | HG00735.hp1 HG01074.hp1 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.738-549G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132913006 | ||||||
chr9:132913125
|
T | A | 1 | a0002c0002t0012g0267 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.738-668A>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132913125 | ||||||
chr9:132913310
|
G | A | 1 | a0001c0007t0006g0199 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.738-853C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132913310 | ||||||
chr9:132913330
|
C | T | 2 | a0001c0001t0027g0226a0001c0001t0027g0227 | 2 | HG02970.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.738-873G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132913330 | ||||||
chr9:132913548
|
C | T | 1 | a0001c0001t0008g0160 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.738-1091G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132913548 | ||||||
chr9:132913587
|
G | A | 4 | a0001c0001t0022g0220a0001c0001t0022g0221a0001c0001t0044g0222others(1): Show | 4 | HG03041.hp2 HG03195.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.738-1130C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132913587 | ||||||
chr9:132913686
|
C | T | 3 | a0001c0001t0006g0196a0001c0001t0006g0200a0001c0001t0006g0201 | 3 | HG02145.hp1 HG03516.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.738-1229G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132913686 | ||||||
chr9:132913688
|
C | T | 1 | a0002c0002t0057g0026 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.738-1231G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132913688 | ||||||
chr9:132913818
|
T | C | 1 | a0001c0001t0078g0135 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.738-1361A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132913818 | ||||||
chr9:132913825
|
C | CA | 41 | a0001c0001t0001g0121a0001c0001t0001g0139a0001c0001t0001g0150others(38): Show | 41 | HG00438.hp2 HG00621.hp1 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.738-1369dupT | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132913825 | ||||||
chr9:132913825
|
CA | C | 11 | a0001c0003t0097g0284a0002c0002t0029g0269a0002c0002t0032g0021others(8): Show | 12 | HG01081.hp1 HG01891.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.738-1369delT | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132913825 | ||||||
chr9:132913844
|
A | AAAAAAAA others(5): Show |
1 | a0002c0009t0093g0303 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.738-1388_738-1387i others(14): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132913844 | ||||||
chr9:132913844
|
A | AAAAAAAA others(4): Show |
1 | a0002c0009t0100g0304 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.738-1388_738-1387i others(13): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132913844 | ||||||
chr9:132913855
|
A | C | 2 | a0002c0009t0093g0303a0002c0009t0100g0304 | 2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.738-1398T>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132913855 | ||||||
chr9:132913873
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.738-1416C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132913873 | ||||||
chr9:132913891
|
G | GT | 55 | a0001c0001t0002g0007a0001c0001t0002g0009a0001c0001t0002g0042others(52): Show | 58 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.738-1435dupA | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132913891 | ||||||
chr9:132913891
|
G | T | 2 | a0001c0003t0009g0276a0002c0002t0057g0026 | 2 | HG01433.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.738-1434C>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132913891 | ||||||
chr9:132913891
|
GT | G | 129 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(126): Show | 149 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(146): Show |
intron_variant | MODIFIER | c.738-1435delA | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132913891 | ||||||
chr9:132913896
|
T | G | 29 | a0001c0001t0001g0119a0001c0001t0001g0129a0001c0001t0001g0130others(26): Show | 30 | HG00423.hp2 HG00621.hp1 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.738-1439A>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132913896 | ||||||
chr9:132913897
|
T | G | 90 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(87): Show | 109 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(106): Show |
intron_variant | MODIFIER | c.738-1440A>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132913897 | ||||||
chr9:132913900
|
T | G | 4 | a0002c0002t0029g0269a0002c0002t0029g0271a0002c0002t0034g0292others(1): Show | 4 | HG01891.hp1 HG02258.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.738-1443A>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132913900 | ||||||
chr9:132913902
|
T | G | 1 | a0001c0001t0078g0135 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.738-1445A>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132913902 | ||||||
chr9:132913903
|
T | G | 3 | a0001c0001t0001g0232a0002c0009t0093g0303a0002c0009t0100g0304 | 3 | HG00673.hp2 HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.738-1446A>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132913903 | ||||||
chr9:132913917
|
T | A | 31 | a0002c0002t0003g0251a0002c0002t0003g0253a0002c0002t0003g0254others(28): Show | 31 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.738-1460A>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132913917 | ||||||
chr9:132913945
|
C | A | 4 | a0002c0002t0014g0247a0002c0002t0014g0248a0002c0002t0014g0249others(1): Show | 4 | HG02257.hp1 HG02280.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.738-1488G>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132913945 | ||||||
chr9:132914232
|
G | A | 4 | a0002c0002t0003g0251a0002c0002t0003g0253a0002c0002t0003g0254others(1): Show | 4 | HG02451.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.738-1775C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132914232 | ||||||
chr9:132914326
|
A | C | 3 | a0001c0001t0053g0117a0001c0001t0055g0116a0001c0001t0056g0118 | 3 | HG01106.hp1 HG02258.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.738-1869T>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132914326 | ||||||
chr9:132914442
|
A | G | 2 | a0002c0002t0003g0253a0002c0002t0003g0254 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.738-1985T>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132914442 | ||||||
chr9:132914514
|
T | C | 1 | a0001c0001t0024g0202 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.738-2057A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132914514 | ||||||
chr9:132914665
|
T | G | 2 | a0001c0001t0024g0188a0001c0001t0024g0202 | 2 | HG03669.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.738-2208A>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132914665 | ||||||
chr9:132914703
|
C | A | 2 | a0001c0001t0001g0189a0001c0001t0001g0190 | 2 | HG02071.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.738-2246G>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132914703 | ||||||
chr9:132914703
|
C | CA | 12 | a0001c0001t0001g0136a0001c0001t0005g0214a0001c0001t0005g0215others(9): Show | 12 | HG01167.hp1 HG02145.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.738-2247dupT | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132914703 | ||||||
chr9:132914703
|
C | CAA | 8 | a0001c0001t0018g0092a0001c0001t0018g0236a0001c0001t0018g0237others(5): Show | 8 | HG00733.hp2 HG01256.hp1 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.738-2248_738-2247d others(4): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132914703 | ||||||
chr9:132914703
|
C | T | 3 | a0001c0001t0001g0121a0001c0001t0001g0183a0001c0001t0001g0191 | 3 | NA18952.hp2 NA18963.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.738-2246G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132914703 | ||||||
chr9:132914703
|
CA | C | 61 | a0001c0001t0027g0226a0001c0001t0027g0227a0001c0001t0033g0023others(58): Show | 61 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.738-2247delT | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132914703 | ||||||
chr9:132914752
|
C | T | 1 | a0001c0001t0056g0118 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.738-2295G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132914752 | ||||||
chr9:132914874
|
G | A | 303 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(300): Show | 335 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(332): Show |
intron_variant | MODIFIER | c.738-2417C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132914874 | ||||||
chr9:132914911
|
C | T | 1 | a0001c0001t0001g0209 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.738-2454G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132914911 | ||||||
chr9:132915089
|
C | T | 2 | a0001c0007t0005g0231a0001c0007t0064g0294 | 2 | HG02055.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.738-2632G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132915089 | ||||||
chr9:132915109
|
C | G | 1 | a0001c0001t0001g0157 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.738-2652G>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132915109 | ||||||
chr9:132915169
|
A | G | 1 | a0001c0001t0051g0156 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.738-2712T>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132915169 | ||||||
chr9:132915176
|
C | G | 1 | a0001c0001t0001g0239 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.738-2719G>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132915176 | ||||||
chr9:132915256
|
G | A | 1 | a0002c0002t0057g0026 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.738-2799C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132915256 | ||||||
chr9:132915551
|
C | T | 2 | a0002c0009t0093g0303a0002c0009t0100g0304 | 2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.738-3094G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132915551 | ||||||
chr9:132915598
|
T | G | 1 | a0001c0001t0018g0092 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.738-3141A>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132915598 | ||||||
chr9:132915716
|
G | A | 118 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(115): Show | 139 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.738-3259C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132915716 | ||||||
chr9:132916095
|
C | A | 2 | a0002c0009t0093g0303a0002c0009t0100g0304 | 2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.738-3638G>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132916095 | ||||||
chr9:132916227
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.738-3770C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132916227 | ||||||
chr9:132916436
|
TA | T | 42 | a0002c0002t0003g0251a0002c0002t0003g0253a0002c0002t0003g0254others(39): Show | 43 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.738-3980delT | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132916436 | ||||||
chr9:132916654
|
G | A | 1 | a0001c0001t0071g0091 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.738-4197C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132916654 | ||||||
chr9:132916679
|
T | C | 4 | a0002c0002t0032g0021a0002c0002t0066g0291a0002c0002t0067g0290others(1): Show | 5 | HG01081.hp1 HG02723.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.738-4222A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132916679 | ||||||
chr9:132916870
|
G | A | 1 | a0002c0002t0098g0235 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.738-4413C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132916870 | ||||||
chr9:132916870
|
G | C | 2 | a0002c0009t0093g0303a0002c0009t0100g0304 | 2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.738-4413C>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132916870 | ||||||
chr9:132916878
|
T | C | 1 | a0001c0001t0005g0033 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.738-4421A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132916878 | ||||||
chr9:132916971
|
C | T | 2 | a0002c0009t0093g0303a0002c0009t0100g0304 | 2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.737+4392G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132916971 | ||||||
chr9:132917026
|
G | A | 1 | a0001c0001t0056g0118 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.737+4337C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132917026 | ||||||
chr9:132917142
|
T | C | 1 | a0001c0001t0004g0174 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.737+4221A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132917142 | ||||||
chr9:132917320
|
C | T | 1 | a0001c0001t0033g0286 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.737+4043G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132917320 | ||||||
chr9:132917393
|
C | T | 101 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(98): Show | 122 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.737+3970G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132917393 | ||||||
chr9:132917464
|
G | T | 1 | a0003c0005t0004g0175 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.737+3899C>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132917464 | ||||||
chr9:132917526
|
T | G | 1 | a0001c0001t0071g0091 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.737+3837A>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132917526 | ||||||
chr9:132917574
|
C | T | 1 | a0001c0001t0001g0182 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.737+3789G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132917574 | ||||||
chr9:132917584
|
C | T | 1 | a0001c0001t0002g0238 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.737+3779G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132917584 | ||||||
chr9:132917648
|
T | A | 163 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(160): Show | 184 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.737+3715A>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132917648 | ||||||
chr9:132918388
|
G | C | 1 | a0002c0002t0086g0260 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.737+2975C>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132918388 | ||||||
chr9:132918437
|
C | G | 3 | a0002c0002t0032g0021a0002c0002t0066g0291a0002c0002t0067g0290 | 4 | HG01081.hp1 HG02723.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.737+2926G>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132918437 | ||||||
chr9:132918464
|
C | T | 1 | a0001c0001t0013g0047 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.737+2899G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132918464 | ||||||
chr9:132918746
|
G | A | 1 | a0001c0001t0018g0092 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.737+2617C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132918746 | ||||||
chr9:132918790
|
G | A | 1 | a0001c0001t0056g0118 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.737+2573C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132918790 | ||||||
chr9:132918818
|
G | A | 1 | a0002c0002t0057g0026 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.737+2545C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132918818 | ||||||
chr9:132918897
|
A | G | 2 | a0002c0009t0093g0303a0002c0009t0100g0304 | 2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.737+2466T>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132918897 | ||||||
chr9:132918907
|
G | A | 1 | a0002c0002t0057g0026 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.737+2456C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132918907 | ||||||
chr9:132919180
|
G | A | 2 | a0005c0010t0043g0224a0005c0010t0043g0225 | 2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.737+2183C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132919180 | ||||||
chr9:132919326
|
A | G | 1 | a0002c0002t0057g0026 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.737+2037T>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132919326 | ||||||
chr9:132919530
|
T | C | 1 | a0002c0002t0034g0292 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.737+1833A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132919530 | ||||||
chr9:132919697
|
C | G | 5 | a0001c0001t0033g0023a0001c0001t0033g0286a0001c0001t0034g0024others(2): Show | 5 | HG00735.hp1 HG01123.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.737+1666G>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132919697 | ||||||
chr9:132920064
|
C | A | 2 | a0002c0002t0003g0253a0002c0002t0003g0254 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.737+1299G>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132920064 | ||||||
chr9:132920250
|
A | C | 1 | a0001c0001t0003g0044 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.737+1113T>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132920250 | ||||||
chr9:132920287
|
C | CAGA | 4 | a0001c0001t0005g0033a0001c0001t0005g0034a0001c0001t0037g0032others(1): Show | 4 | HG02647.hp1 HG02895.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.737+1075_737+1076i others(5): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132920287 | ||||||
chr9:132920397
|
G | A | 1 | a0001c0001t0005g0034 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.737+966C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132920397 | ||||||
chr9:132920484
|
A | G | 1 | a0002c0002t0074g0265 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.737+879T>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132920484 | ||||||
chr9:132920745
|
G | A | 2 | a0001c0001t0015g0036a0001c0001t0015g0037 | 2 | HG02965.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.737+618C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132920745 | ||||||
chr9:132920795
|
C | T | 44 | a0001c0001t0027g0226a0001c0001t0027g0227a0002c0002t0003g0251others(41): Show | 45 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.737+568G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132920795 | ||||||
chr9:132920802
|
A | G | 2 | a0002c0009t0093g0303a0002c0009t0100g0304 | 2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.737+561T>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132920802 | ||||||
chr9:132920858
|
C | G | 2 | a0002c0009t0093g0303a0002c0009t0100g0304 | 2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.737+505G>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132920858 | ||||||
chr9:132920862
|
G | T | 4 | a0001c0001t0015g0036a0001c0001t0015g0037a0001c0001t0015g0272others(1): Show | 4 | HG02818.hp2 HG02965.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.737+501C>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132920862 | ||||||
chr9:132920893
|
G | A | 1 | a0001c0001t0078g0135 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.737+470C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132920893 | ||||||
chr9:132920972
|
C | T | 2 | a0002c0009t0093g0303a0002c0009t0100g0304 | 2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.737+391G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132920972 | ||||||
chr9:132921080
|
T | C | 1 | a0002c0002t0074g0265 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.737+283A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132921080 | ||||||
chr9:132921114
|
G | A | 1 | a0002c0002t0070g0263 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.737+249C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132921114 | ||||||
chr9:132921130
|
G | A | 3 | a0002c0002t0029g0269a0002c0002t0029g0271a0002c0002t0080g0270 | 3 | HG01891.hp1 HG02258.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.737+233C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132921130 | ||||||
chr9:132921221
|
A | C | 1 | a0002c0013t0087g0293 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.737+142T>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132921221 | ||||||
chr9:132921235
|
T | C | 1 | a0001c0001t0015g0272 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.737+128A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 8/22 | chr9 | 132921235 | ||||||
chr9:132921544
|
T | C | 2 | a0002c0009t0093g0303a0002c0009t0100g0304 | 2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.664-108A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 7/22 | chr9 | 132921544 | ||||||
chr9:132921562
|
G | A | 2 | a0002c0009t0093g0303a0002c0009t0100g0304 | 2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.664-126C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 7/22 | chr9 | 132921562 | ||||||
chr9:132922067
|
T | G | 1 | a0001c0001t0002g0093 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.509-94A>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 6/22 | chr9 | 132922067 | ||||||
chr9:132922073
|
A | G | 2 | a0002c0009t0093g0303a0002c0009t0100g0304 | 2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.509-100T>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 6/22 | chr9 | 132922073 | ||||||
chr9:132922203
|
T | C | 1 | a0002c0002t0098g0235 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.509-230A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 6/22 | chr9 | 132922203 | ||||||
chr9:132922268
|
A | G | 1 | a0001c0001t0036g0006 | 2 | NA18939.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.509-295T>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 6/22 | chr9 | 132922268 | ||||||
chr9:132922324
|
G | A | 2 | a0002c0009t0093g0303a0002c0009t0100g0304 | 2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.509-351C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 6/22 | chr9 | 132922324 | ||||||
chr9:132922607
|
C | T | 11 | a0001c0001t0005g0033a0001c0001t0005g0034a0001c0001t0006g0195others(8): Show | 11 | HG02145.hp1 HG02451.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.509-634G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 6/22 | chr9 | 132922607 | ||||||
chr9:132922750
|
G | A | 1 | a0001c0001t0003g0295 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.508+598C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 6/22 | chr9 | 132922750 | ||||||
chr9:132922803
|
A | G | 1 | a0002c0002t0034g0292 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.508+545T>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 6/22 | chr9 | 132922803 | ||||||
chr9:132922952
|
C | T | 1 | a0001c0001t0001g0020 | 2 | HG01106.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.508+396G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 6/22 | chr9 | 132922952 | ||||||
chr9:132922995
|
G | A | 2 | a0001c0001t0055g0116a0001c0001t0056g0118 | 2 | HG01106.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.508+353C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 6/22 | chr9 | 132922995 | ||||||
chr9:132923051
|
C | T | 2 | a0002c0009t0093g0303a0002c0009t0100g0304 | 2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.508+297G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 6/22 | chr9 | 132923051 | ||||||
chr9:132923055
|
C | T | 1 | a0002c0002t0098g0235 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.508+293G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 6/22 | chr9 | 132923055 | ||||||
chr9:132923120
|
C | A | 4 | a0001c0001t0022g0220a0001c0001t0022g0221a0001c0001t0044g0222others(1): Show | 4 | HG03041.hp2 HG03195.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.508+228G>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 6/22 | chr9 | 132923120 | ||||||
chr9:132923120
|
C | T | 1 | a0001c0003t0030g0274 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.508+228G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 6/22 | chr9 | 132923120 | ||||||
chr9:132923249
|
A | G | 1 | a0001c0001t0061g0110 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.508+99T>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 6/22 | chr9 | 132923249 | ||||||
chr9:132923334
|
G | A | 1 | a0002c0002t0012g0255 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.508+14C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 6/22 | chr9 | 132923334 | ||||||
chr9:132923611
|
C | T | 2 | a0002c0009t0093g0303a0002c0009t0100g0304 | 2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.364-119G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 5/22 | chr9 | 132923611 | ||||||
chr9:132923905
|
TGTTA | T | 4 | a0002c0002t0029g0269a0002c0002t0029g0271a0002c0002t0034g0292others(1): Show | 4 | HG01891.hp1 HG02258.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.364-417_364-414del others(4): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 5/22 | chr9 | 132923905 | ||||||
chr9:132923912
|
T | TA | 8 | a0001c0001t0006g0195a0001c0001t0006g0197a0001c0001t0006g0200others(5): Show | 8 | HG01106.hp1 HG02145.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.364-421dupT | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 5/22 | chr9 | 132923912 | ||||||
chr9:132924061
|
A | AAT | 189 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(186): Show | 211 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.364-571_364-570dup others(2): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 5/22 | chr9 | 132924061 | ||||||
chr9:132924299
|
T | C | 1 | a0001c0003t0097g0284 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.364-807A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 5/22 | chr9 | 132924299 | ||||||
chr9:132924309
|
T | C | 1 | a0002c0002t0057g0026 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.364-817A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 5/22 | chr9 | 132924309 | ||||||
chr9:132924389
|
G | A | 27 | a0001c0001t0001g0137a0001c0001t0033g0023a0001c0001t0033g0286others(24): Show | 27 | HG00735.hp1 HG01074.hp1 HG01123.hp1 others(24): Show |
intron_variant | MODIFIER | c.364-897C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 5/22 | chr9 | 132924389 | ||||||
chr9:132924530
|
G | T | 191 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(188): Show | 213 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(210): Show |
intron_variant | MODIFIER | c.364-1038C>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 5/22 | chr9 | 132924530 | ||||||
chr9:132924542
|
A | C | 3 | a0001c0001t0053g0117a0001c0007t0005g0231a0001c0007t0064g0294 | 3 | HG02055.hp1 HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.363+1045T>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 5/22 | chr9 | 132924542 | ||||||
chr9:132924547
|
A | G | 1 | a0002c0002t0032g0021 | 2 | HG02723.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.363+1040T>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 5/22 | chr9 | 132924547 | ||||||
chr9:132924554
|
T | C | 2 | a0005c0010t0043g0224a0005c0010t0043g0225 | 2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.363+1033A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 5/22 | chr9 | 132924554 | ||||||
chr9:132924617
|
A | G | 44 | a0001c0001t0027g0226a0001c0001t0027g0227a0002c0002t0003g0251others(41): Show | 45 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.363+970T>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 5/22 | chr9 | 132924617 | ||||||
chr9:132924938
|
C | T | 5 | a0001c0001t0003g0044a0001c0001t0003g0045a0001c0001t0003g0107others(2): Show | 5 | NA18951.hp1 NA18965.hp1 NA18972.hp1 others(2): Show |
intron_variant | MODIFIER | c.363+649G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 5/22 | chr9 | 132924938 | ||||||
chr9:132925249
|
T | C | 1 | a0002c0002t0098g0235 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.363+338A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 5/22 | chr9 | 132925249 | ||||||
chr9:132925375
|
C | T | 2 | a0002c0009t0093g0303a0002c0009t0100g0304 | 2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.363+212G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 5/22 | chr9 | 132925375 | ||||||
chr9:132925801
|
G | C | 1 | a0001c0001t0001g0180 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.211-62C>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 4/22 | chr9 | 132925801 | ||||||
chr9:132926025
|
A | G | 2 | a0002c0002t0066g0291a0002c0002t0067g0290 | 2 | HG01081.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.211-286T>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 4/22 | chr9 | 132926025 | ||||||
chr9:132926073
|
A | C | 1 | a0001c0001t0001g0022 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.211-334T>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 4/22 | chr9 | 132926073 | ||||||
chr9:132926494
|
C | T | 1 | a0001c0001t0099g0112 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.210+707G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 4/22 | chr9 | 132926494 | ||||||
chr9:132926572
|
G | A | 2 | a0001c0001t0027g0226a0001c0001t0027g0227 | 2 | HG02970.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.210+629C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 4/22 | chr9 | 132926572 | ||||||
chr9:132926644
|
C | T | 2 | a0002c0009t0093g0303a0002c0009t0100g0304 | 2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.210+557G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 4/22 | chr9 | 132926644 | ||||||
chr9:132926685
|
CT | C | 103 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(100): Show | 124 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.210+515delA | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 4/22 | chr9 | 132926685 | ||||||
chr9:132926689
|
T | G | 44 | a0001c0001t0027g0226a0001c0001t0027g0227a0002c0002t0003g0251others(41): Show | 45 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.210+512A>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 4/22 | chr9 | 132926689 | ||||||
chr9:132926703
|
A | G | 8 | a0001c0001t0001g0020a0001c0001t0001g0153a0001c0001t0001g0154others(5): Show | 9 | HG01099.hp2 HG01106.hp2 HG01167.hp2 others(6): Show |
intron_variant | MODIFIER | c.210+498T>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 4/22 | chr9 | 132926703 | ||||||
chr9:132926777
|
C | T | 2 | a0002c0009t0093g0303a0002c0009t0100g0304 | 2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.210+424G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 4/22 | chr9 | 132926777 | ||||||
chr9:132926799
|
T | C | 1 | a0001c0001t0061g0110 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.210+402A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 4/22 | chr9 | 132926799 | ||||||
chr9:132926911
|
A | G | 113 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(110): Show | 134 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.210+290T>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 4/22 | chr9 | 132926911 | ||||||
chr9:132927168
|
C | T | 1 | a0001c0001t0061g0110 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.210+33G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 4/22 | chr9 | 132927168 | ||||||
chr9:132927452
|
T | G | 30 | a0002c0002t0003g0251a0002c0002t0003g0253a0002c0002t0003g0254others(27): Show | 30 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.107-148A>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 3/22 | chr9 | 132927452 | ||||||
chr9:132927521
|
C | CT | 114 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(111): Show | 134 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.107-218dupA | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 3/22 | chr9 | 132927521 | ||||||
chr9:132927521
|
C | CTT | 14 | a0001c0001t0001g0139a0001c0001t0001g0151a0001c0001t0001g0232others(11): Show | 15 | HG00673.hp2 HG01255.hp2 HG02056.hp1 others(12): Show |
intron_variant | MODIFIER | c.107-219_107-218dup others(2): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 3/22 | chr9 | 132927521 | ||||||
chr9:132927521
|
C | CTTT | 25 | a0001c0001t0027g0227a0002c0002t0003g0251a0002c0002t0003g0253others(22): Show | 25 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(22): Show |
intron_variant | MODIFIER | c.107-220_107-218dup others(3): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 3/22 | chr9 | 132927521 | ||||||
chr9:132927521
|
C | CTTTT | 10 | a0001c0001t0027g0226a0002c0002t0012g0266a0002c0002t0029g0269others(7): Show | 10 | HG00639.hp1 HG01081.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.107-221_107-218dup others(4): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 3/22 | chr9 | 132927521 | ||||||
chr9:132927683
|
C | T | 1 | a0001c0001t0055g0116 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.107-379G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 3/22 | chr9 | 132927683 | ||||||
chr9:132927772
|
G | A | 22 | a0001c0001t0001g0137a0001c0003t0009g0276a0001c0003t0009g0281others(19): Show | 22 | HG01074.hp1 HG01175.hp1 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.107-468C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 3/22 | chr9 | 132927772 | ||||||
chr9:132927779
|
C | A | 3 | a0001c0001t0053g0117a0001c0001t0055g0116a0001c0001t0056g0118 | 3 | HG01106.hp1 HG02258.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.107-475G>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 3/22 | chr9 | 132927779 | ||||||
chr9:132927845
|
C | T | 1 | a0001c0001t0078g0135 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.107-541G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 3/22 | chr9 | 132927845 | ||||||
chr9:132927922
|
C | A | 1 | a0002c0002t0057g0026 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.107-618G>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 3/22 | chr9 | 132927922 | ||||||
chr9:132928134
|
G | A | 3 | a0001c0001t0001g0191a0002c0002t0038g0301a0002c0002t0038g0302 | 3 | HG02572.hp1 HG02630.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.106+633C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 3/22 | chr9 | 132928134 | ||||||
chr9:132928369
|
A | C | 2 | a0002c0009t0093g0303a0002c0009t0100g0304 | 2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.106+398T>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 3/22 | chr9 | 132928369 | ||||||
chr9:132928580
|
C | A | 2 | a0005c0010t0043g0224a0005c0010t0043g0225 | 2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.106+187G>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 3/22 | chr9 | 132928580 | ||||||
chr9:132928597
|
C | G | 1 | a0002c0002t0012g0266 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.106+170G>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 3/22 | chr9 | 132928597 | ||||||
chr9:132928679
|
A | T | 1 | a0001c0001t0001g0180 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.106+88T>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 3/22 | chr9 | 132928679 | ||||||
chr9:132928752
|
T | C | 10 | a0001c0001t0001g0013a0001c0001t0001g0119a0001c0001t0001g0120others(7): Show | 11 | HG00558.hp1 NA18952.hp1 NA18984.hp2 others(8): Show |
intron_variant | MODIFIER | c.106+15A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 3/22 | chr9 | 132928752 | ||||||
chr9:132929039
|
G | A | 1 | a0001c0001t0054g0115 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-80-87C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132929039 | ||||||
chr9:132929161
|
C | T | 1 | a0001c0001t0006g0195 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-80-209G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132929161 | ||||||
chr9:132929187
|
T | G | 2 | a0001c0001t0001g0177a0003c0005t0001g0178 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.-80-235A>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132929187 | ||||||
chr9:132929322
|
T | G | 1 | a0001c0001t0002g0095 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-80-370A>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132929322 | ||||||
chr9:132929331
|
C | T | 1 | a0002c0002t0032g0021 | 2 | HG02723.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.-80-379G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132929331 | ||||||
chr9:132929348
|
T | C | 113 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(110): Show | 134 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.-80-396A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132929348 | ||||||
chr9:132929355
|
TC | T | 4 | a0001c0001t0003g0229a0001c0001t0003g0295a0001c0001t0010g0230others(1): Show | 4 | HG00323.hp2 NA18946.hp1 NA19086.hp1 others(1): Show |
intron_variant | MODIFIER | c.-80-404delG | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132929355 | ||||||
chr9:132929522
|
G | A | 30 | a0002c0002t0003g0251a0002c0002t0003g0253a0002c0002t0003g0254others(27): Show | 30 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.-80-570C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132929522 | ||||||
chr9:132929760
|
A | AC | 7 | a0001c0001t0006g0195a0001c0001t0006g0196a0001c0001t0006g0197others(4): Show | 7 | HG02145.hp1 HG02451.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.-80-809_-80-808ins others(1): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132929760 | ||||||
chr9:132930220
|
A | C | 37 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(34): Show | 42 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.-80-1268T>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132930220 | ||||||
chr9:132930587
|
C | CA | 99 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(96): Show | 120 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.-80-1636dupT | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132930587 | ||||||
chr9:132930587
|
C | CAA | 66 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0180others(63): Show | 66 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-1637_-80-1636d others(4): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132930587 | ||||||
chr9:132930587
|
C | CAAA | 12 | a0001c0001t0001g0192a0001c0001t0001g0212a0001c0001t0006g0200others(9): Show | 12 | HG02145.hp1 HG02572.hp1 HG02970.hp2 others(9): Show |
intron_variant | MODIFIER | c.-80-1638_-80-1636d others(5): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132930587 | ||||||
chr9:132930920
|
T | G | 1 | a0002c0002t0086g0260 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-80-1968A>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132930920 | ||||||
chr9:132930971
|
A | G | 1 | a0001c0001t0025g0040 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-80-2019T>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132930971 | ||||||
chr9:132930980
|
C | A | 1 | a0001c0001t0078g0135 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-80-2028G>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132930980 | ||||||
chr9:132931261
|
G | A | 1 | a0001c0001t0002g0109 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-80-2309C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132931261 | ||||||
chr9:132931384
|
G | A | 4 | a0002c0002t0029g0269a0002c0002t0029g0271a0002c0002t0034g0292others(1): Show | 4 | HG01891.hp1 HG02258.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-80-2432C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132931384 | ||||||
chr9:132931475
|
T | C | 4 | a0001c0001t0022g0220a0001c0001t0022g0221a0001c0001t0044g0222others(1): Show | 4 | HG03041.hp2 HG03195.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.-80-2523A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132931475 | ||||||
chr9:132931606
|
G | A | 1 | a0001c0001t0050g0193 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-80-2654C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132931606 | ||||||
chr9:132931761
|
G | C | 1 | a0002c0002t0005g0261 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-80-2809C>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132931761 | ||||||
chr9:132932013
|
C | G | 1 | a0001c0001t0063g0039 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-81+3020G>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132932013 | ||||||
chr9:132932027
|
C | T | 1 | a0002c0013t0087g0293 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-81+3006G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132932027 | ||||||
chr9:132932358
|
A | G | 1 | a0002c0002t0032g0021 | 2 | HG02723.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.-81+2675T>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132932358 | ||||||
chr9:132932430
|
G | A | 1 | a0001c0001t0034g0024 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-81+2603C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132932430 | ||||||
chr9:132932593
|
T | G | 1 | a0001c0001t0001g0194 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-81+2440A>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132932593 | ||||||
chr9:132932635
|
G | T | 1 | a0002c0013t0087g0293 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-81+2398C>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132932635 | ||||||
chr9:132933010
|
G | A | 4 | a0001c0001t0005g0033a0001c0001t0005g0034a0001c0001t0037g0032others(1): Show | 4 | HG02647.hp1 HG02895.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-81+2023C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132933010 | ||||||
chr9:132933444
|
GT | G | 35 | a0002c0002t0003g0251a0002c0002t0003g0253a0002c0002t0003g0254others(32): Show | 36 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.-81+1588delA | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132933444 | ||||||
chr9:132933471
|
T | C | 30 | a0002c0002t0003g0251a0002c0002t0003g0253a0002c0002t0003g0254others(27): Show | 30 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.-81+1562A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132933471 | ||||||
chr9:132933474
|
C | T | 102 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(99): Show | 123 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.-81+1559G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132933474 | ||||||
chr9:132933513
|
G | A | 1 | a0001c0001t0024g0202 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-81+1520C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132933513 | ||||||
chr9:132933682
|
G | A | 2 | a0001c0001t0082g0289a0001c0001t0083g0264 | 2 | HG00735.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.-81+1351C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132933682 | ||||||
chr9:132933998
|
T | C | 2 | a0002c0002t0070g0263a0002c0002t0075g0262 | 2 | NA19065.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.-81+1035A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132933998 | ||||||
chr9:132934008
|
T | C | 2 | a0001c0001t0001g0203a0001c0001t0001g0239 | 2 | HG02080.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.-81+1025A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132934008 | ||||||
chr9:132934194
|
C | A | 1 | a0002c0002t0098g0235 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-81+839G>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132934194 | ||||||
chr9:132934329
|
C | T | 1 | a0001c0001t0001g0137 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-81+704G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132934329 | ||||||
chr9:132934466
|
C | T | 1 | a0001c0001t0001g0136 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-81+567G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132934466 | ||||||
chr9:132934557
|
G | A | 1 | a0001c0001t0061g0110 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-81+476C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132934557 | ||||||
chr9:132934861
|
T | G | 1 | a0001c0006t0020g0111 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-81+172A>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132934861 | ||||||
chr9:132934947
|
G | A | 1 | a0002c0002t0012g0266 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-81+86C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 2/22 | chr9 | 132934947 | ||||||
chr9:132935112
|
T | C | 2 | a0002c0009t0093g0303a0002c0009t0100g0304 | 2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-143-17A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132935112 | ||||||
chr9:132935209
|
C | G | 1 | a0002c0002t0057g0026 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-143-114G>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132935209 | ||||||
chr9:132935250
|
C | T | 2 | a0002c0009t0093g0303a0002c0009t0100g0304 | 2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-143-155G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132935250 | ||||||
chr9:132935552
|
T | C | 2 | a0002c0009t0093g0303a0002c0009t0100g0304 | 2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-143-457A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132935552 | ||||||
chr9:132935623
|
G | C | 4 | a0001c0001t0053g0117a0001c0001t0054g0115a0001c0001t0055g0116others(1): Show | 4 | HG01106.hp1 HG02258.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.-143-528C>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132935623 | ||||||
chr9:132935664
|
C | T | 2 | a0001c0001t0007g0038a0004c0011t0007g0005 | 3 | HG02559.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-143-569G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132935664 | ||||||
chr9:132935714
|
C | T | 2 | a0002c0009t0093g0303a0002c0009t0100g0304 | 2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-143-619G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132935714 | ||||||
chr9:132935771
|
C | T | 1 | a0001c0001t0078g0135 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-143-676G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132935771 | ||||||
chr9:132935870
|
A | C | 1 | a0002c0013t0087g0293 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-143-775T>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132935870 | ||||||
chr9:132935882
|
C | T | 7 | a0001c0001t0001g0014a0001c0001t0001g0130a0001c0001t0001g0132others(4): Show | 8 | HG02165.hp2 NA18946.hp2 NA18948.hp1 others(5): Show |
intron_variant | MODIFIER | c.-143-787G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132935882 | ||||||
chr9:132936041
|
C | A | 1 | a0001c0001t0001g0204 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-143-946G>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132936041 | ||||||
chr9:132936396
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-143-1301G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132936396 | ||||||
chr9:132936423
|
T | C | 1 | a0001c0001t0001g0020 | 2 | HG01106.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.-143-1328A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132936423 | ||||||
chr9:132936550
|
T | C | 3 | a0001c0001t0053g0117a0001c0001t0055g0116a0001c0001t0056g0118 | 3 | HG01106.hp1 HG02258.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.-143-1455A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132936550 | ||||||
chr9:132936892
|
G | A | 3 | a0002c0002t0032g0021a0002c0002t0066g0291a0002c0002t0067g0290 | 4 | HG01081.hp1 HG02723.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.-143-1797C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132936892 | ||||||
chr9:132937028
|
C | G | 1 | a0002c0002t0040g0128 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-143-1933G>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132937028 | ||||||
chr9:132937100
|
G | A | 1 | a0002c0002t0057g0026 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-143-2005C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132937100 | ||||||
chr9:132937173
|
G | A | 2 | a0002c0002t0066g0291a0002c0002t0067g0290 | 2 | HG01081.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-143-2078C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132937173 | ||||||
chr9:132937181
|
C | A | 2 | a0002c0009t0093g0303a0002c0009t0100g0304 | 2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-143-2086G>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132937181 | ||||||
chr9:132937181
|
C | G | 29 | a0002c0002t0003g0251a0002c0002t0003g0253a0002c0002t0003g0254others(26): Show | 29 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(26): Show |
intron_variant | MODIFIER | c.-143-2086G>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132937181 | ||||||
chr9:132937304
|
G | A | 1 | a0001c0001t0041g0113 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-143-2209C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132937304 | ||||||
chr9:132937335
|
C | T | 2 | a0001c0001t0015g0036a0001c0001t0015g0037 | 2 | HG02965.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-143-2240G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132937335 | ||||||
chr9:132937336
|
G | C | 67 | a0001c0001t0033g0023a0001c0001t0033g0286a0001c0001t0034g0024others(64): Show | 68 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.-143-2241C>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132937336 | ||||||
chr9:132937439
|
G | A | 3 | a0001c0001t0005g0214a0001c0001t0005g0215a0001c0001t0005g0216 | 3 | HG01167.hp1 HG02145.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.-143-2344C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132937439 | ||||||
chr9:132937592
|
A | T | 2 | a0005c0010t0043g0224a0005c0010t0043g0225 | 2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-143-2497T>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132937592 | ||||||
chr9:132937614
|
C | T | 60 | a0001c0001t0033g0023a0001c0001t0033g0286a0001c0001t0034g0024others(57): Show | 61 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.-143-2519G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132937614 | ||||||
chr9:132937692
|
G | A | 2 | a0002c0009t0093g0303a0002c0009t0100g0304 | 2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-143-2597C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132937692 | ||||||
chr9:132937800
|
C | T | 2 | a0002c0009t0093g0303a0002c0009t0100g0304 | 2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-143-2705G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132937800 | ||||||
chr9:132937941
|
C | T | 1 | a0001c0006t0002g0035 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-143-2846G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132937941 | ||||||
chr9:132938071
|
T | C | 2 | a0001c0001t0053g0117a0001c0001t0056g0118 | 2 | HG02258.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.-143-2976A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132938071 | ||||||
chr9:132938251
|
T | C | 1 | a0006c0017t0001g0205 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-143-3156A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132938251 | ||||||
chr9:132938330
|
G | A | 1 | a0002c0013t0087g0293 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-143-3235C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132938330 | ||||||
chr9:132938534
|
G | A | 2 | a0005c0010t0043g0224a0005c0010t0043g0225 | 2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-143-3439C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132938534 | ||||||
chr9:132938701
|
C | T | 1 | a0001c0003t0081g0268 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-143-3606G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132938701 | ||||||
chr9:132938744
|
C | A | 1 | a0001c0001t0001g0206 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-143-3649G>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132938744 | ||||||
chr9:132938825
|
T | C | 1 | a0001c0001t0011g0114 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-143-3730A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132938825 | ||||||
chr9:132938879
|
G | A | 1 | a0002c0013t0087g0293 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-143-3784C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132938879 | ||||||
chr9:132938994
|
A | G | 2 | a0002c0009t0093g0303a0002c0009t0100g0304 | 2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-143-3899T>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132938994 | ||||||
chr9:132939296
|
G | T | 29 | a0002c0002t0003g0251a0002c0002t0003g0253a0002c0002t0003g0254others(26): Show | 29 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(26): Show |
intron_variant | MODIFIER | c.-143-4201C>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132939296 | ||||||
chr9:132939882
|
T | C | 194 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(191): Show | 216 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.-144+4661A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132939882 | ||||||
chr9:132939933
|
C | T | 10 | a0001c0001t0001g0013a0001c0001t0001g0119a0001c0001t0001g0120others(7): Show | 11 | HG00558.hp1 NA18952.hp1 NA18984.hp2 others(8): Show |
intron_variant | MODIFIER | c.-144+4610G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132939933 | ||||||
chr9:132940087
|
T | G | 115 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(112): Show | 136 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.-144+4456A>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132940087 | ||||||
chr9:132940239
|
TA | T | 8 | a0001c0001t0005g0033a0001c0001t0005g0034a0001c0001t0011g0030others(5): Show | 8 | HG02280.hp2 HG02486.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.-144+4303delT | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132940239 | ||||||
chr9:132940485
|
T | G | 1 | a0001c0001t0020g0207 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-144+4058A>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132940485 | ||||||
chr9:132940533
|
T | C | 1 | a0002c0002t0074g0265 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-144+4010A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132940533 | ||||||
chr9:132940753
|
T | A | 5 | a0001c0001t0001g0209a0001c0001t0001g0211a0001c0001t0001g0212others(2): Show | 5 | NA18941.hp2 NA18960.hp2 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.-144+3790A>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132940753 | ||||||
chr9:132940878
|
C | A | 1 | a0001c0007t0064g0294 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-144+3665G>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132940878 | ||||||
chr9:132941217
|
T | C | 1 | a0001c0001t0002g0213 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-144+3326A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132941217 | ||||||
chr9:132941232
|
G | A | 3 | a0001c0001t0005g0214a0001c0001t0005g0215a0001c0001t0005g0216 | 3 | HG01167.hp1 HG02145.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.-144+3311C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132941232 | ||||||
chr9:132941234
|
A | G | 2 | a0005c0010t0043g0224a0005c0010t0043g0225 | 2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-144+3309T>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132941234 | ||||||
chr9:132941498
|
A | G | 71 | a0001c0001t0027g0226a0001c0001t0027g0227a0001c0001t0033g0023others(68): Show | 72 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.-144+3045T>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132941498 | ||||||
chr9:132941512
|
A | C | 1 | a0001c0001t0003g0028 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-144+3031T>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132941512 | ||||||
chr9:132941923
|
C | T | 1 | a0001c0001t0048g0027 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-144+2620G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132941923 | ||||||
chr9:132941969
|
C | T | 2 | a0002c0009t0093g0303a0002c0009t0100g0304 | 2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-144+2574G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132941969 | ||||||
chr9:132942390
|
T | G | 3 | a0001c0001t0039g0217a0001c0001t0039g0218a0001c0001t0088g0219 | 3 | HG00733.hp2 HG01516.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.-144+2153A>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132942390 | ||||||
chr9:132942406
|
G | A | 3 | a0001c0001t0022g0220a0001c0001t0022g0221a0001c0001t0044g0222 | 3 | HG03195.hp2 NA18906.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-144+2137C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132942406 | ||||||
chr9:132942467
|
T | C | 1 | a0002c0002t0012g0266 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-144+2076A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132942467 | ||||||
chr9:132942571
|
T | C | 1 | a0001c0001t0001g0223 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-144+1972A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132942571 | ||||||
chr9:132943231
|
T | TA | 64 | a0001c0001t0003g0229a0001c0001t0003g0295a0001c0001t0010g0230others(61): Show | 64 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.-144+1311dupT | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132943231 | ||||||
chr9:132943231
|
T | TAA | 7 | a0001c0003t0031g0298a0001c0003t0031g0300a0001c0003t0035g0297others(4): Show | 8 | HG01074.hp1 HG01175.hp1 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.-144+1310_-144+131 others(6): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132943231 | ||||||
chr9:132943275
|
C | CTTCAGTA others(16): Show |
1 | a0002c0002t0057g0026 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-144+1245_-144+126 others(27): Show |
TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132943275 | ||||||
chr9:132943294
|
T | C | 2 | a0001c0001t0001g0232a0001c0001t0001g0233 | 2 | HG00673.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.-144+1249A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132943294 | ||||||
chr9:132943316
|
T | A | 1 | a0001c0001t0001g0234 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-144+1227A>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132943316 | ||||||
chr9:132943317
|
T | A | 1 | a0001c0001t0001g0234 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-144+1226A>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132943317 | ||||||
chr9:132943424
|
C | A | 1 | a0002c0002t0032g0021 | 2 | HG02723.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.-144+1119G>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132943424 | ||||||
chr9:132943511
|
C | G | 1 | a0001c0001t0007g0025 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-144+1032G>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132943511 | ||||||
chr9:132943522
|
G | C | 2 | a0002c0009t0093g0303a0002c0009t0100g0304 | 2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-144+1021C>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132943522 | ||||||
chr9:132943625
|
T | C | 1 | a0002c0002t0098g0235 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-144+918A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132943625 | ||||||
chr9:132943733
|
C | A | 2 | a0001c0001t0018g0236a0001c0001t0018g0237 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-144+810G>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132943733 | ||||||
chr9:132943791
|
A | C | 2 | a0002c0009t0093g0303a0002c0009t0100g0304 | 2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-144+752T>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132943791 | ||||||
chr9:132943980
|
C | T | 2 | a0002c0009t0093g0303a0002c0009t0100g0304 | 2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-144+563G>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132943980 | ||||||
chr9:132944033
|
G | T | 32 | a0001c0001t0001g0239a0001c0001t0002g0238a0001c0001t0083g0264others(29): Show | 32 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.-144+510C>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132944033 | ||||||
chr9:132944097
|
T | C | 2 | a0002c0002t0038g0301a0002c0002t0038g0302 | 2 | HG02572.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.-144+446A>G | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132944097 | ||||||
chr9:132944192
|
G | T | 2 | a0001c0001t0033g0023a0001c0001t0034g0024 | 2 | HG02886.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-144+351C>A | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132944192 | ||||||
chr9:132944194
|
G | A | 66 | a0001c0001t0001g0239a0001c0001t0002g0238a0001c0001t0003g0295others(63): Show | 67 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.-144+349C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132944194 | ||||||
chr9:132944373
|
G | A | 2 | a0002c0009t0093g0303a0002c0009t0100g0304 | 2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-144+170C>T | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132944373 | ||||||
chr9:132944441
|
C | G | 1 | a0001c0001t0001g0022 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-144+102G>C | TSC1 | ENSG00000165699.15 | transcript | ENST00000298552.9 | protein_coding | 1/22 | chr9 | 132944441 |