geneid | 150465 |
---|---|
ensemblid | ENSG00000114999.8 |
hgncid | 21586 |
symbol | TTL |
name | tubulin tyrosine ligase |
refseq_nuc | NM_153712.5 |
refseq_prot | NP_714923.1 |
ensembl_nuc | ENST00000233336.7 |
ensembl_prot | ENSP00000233336.5 |
mane_status | MANE Select |
chr | chr2 |
start | 112482156 |
end | 112541739 |
strand | + |
ver | v1.2 |
region | chr2:112482156-112541739 |
region5000 | chr2:112477156-112546739 |
regionname0 | TTL_chr2_112482156_112541739 |
regionname5000 | TTL_chr2_112477156_112546739 |
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 | 0/0 | 377 | 345 | 98 | 62 | 143 | 12 | 30 | 110 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0002 | 0/0 | 377 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
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 | 0/0 | 1134 | 159 | 48 | 30 | 57 | 6 | 18 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
c0002 | 0/0 | 1134 | 103 | 37 | 20 | 34 | 5 | 7 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
c0003 | 0/0 | 1134 | 81 | 13 | 10 | 52 | 1 | 5 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
c0004 | 0/0 | 1134 | 2 | 0 | 2 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
c0005 | 0/0 | 1134 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
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 | 13148 | 50 | 2 | 16 | 21 | 4 | 7 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0002 | 0/0 | 13150 | 33 | 0 | 9 | 21 | 1 | 2 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0003 | 0/0 | 13151 | 18 | 0 | 1 | 16 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0004 | 0/0 | 13152 | 16 | 8 | 3 | 5 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0005 | 0/0 | 13150 | 10 | 0 | 1 | 9 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0006 | 0/0 | 13156 | 8 | 8 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0007 | 0/0 | 13134 | 8 | 7 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0008 | 0/0 | 13148 | 6 | 0 | 1 | 0 | 3 | 2 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0009 | 0/0 | 13149 | 6 | 4 | 2 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0010 | 0/0 | 13151 | 6 | 0 | 0 | 6 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0011 | 0/0 | 13151 | 5 | 0 | 0 | 5 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0012 | 0/0 | 13157 | 4 | 4 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0013 | 0/0 | 13148 | 4 | 0 | 0 | 3 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0014 | 0/0 | 13148 | 4 | 3 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0015 | 0/0 | 13128 | 3 | 3 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0016 | 0/0 | 13148 | 3 | 0 | 0 | 3 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0017 | 0/0 | 13149 | 3 | 0 | 0 | 1 | 0 | 2 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0018 | 0/0 | 13147 | 3 | 0 | 0 | 3 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0019 | 0/0 | 13151 | 3 | 0 | 0 | 3 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0020 | 0/0 | 13150 | 3 | 3 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0021 | 0/0 | 13152 | 3 | 0 | 0 | 0 | 1 | 2 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0022 | 0/0 | 13151 | 3 | 0 | 0 | 3 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0023 | 0/0 | 13151 | 3 | 2 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0024 | 0/0 | 13152 | 3 | 2 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0025 | 0/0 | 13149 | 3 | 0 | 3 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0026 | 0/0 | 13152 | 3 | 1 | 1 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0027 | 0/0 | 13151 | 3 | 0 | 0 | 3 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0028 | 0/0 | 13155 | 2 | 2 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0029 | 0/0 | 13143 | 2 | 1 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0030 | 0/0 | 13151 | 2 | 0 | 0 | 0 | 1 | 1 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0031 | 0/0 | 13151 | 2 | 0 | 0 | 2 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0032 | 0/0 | 13152 | 2 | 1 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0033 | 0/0 | 13151 | 2 | 0 | 1 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0034 | 0/0 | 13153 | 2 | 0 | 0 | 1 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0035 | 0/0 | 13152 | 2 | 0 | 0 | 1 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0036 | 0/0 | 13136 | 2 | 0 | 0 | 2 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0037 | 0/0 | 13153 | 2 | 0 | 0 | 2 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0038 | 0/0 | 13152 | 2 | 0 | 0 | 2 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0039 | 0/0 | 13149 | 2 | 0 | 1 | 0 | 1 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0040 | 0/0 | 13148 | 2 | 2 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0041 | 0/0 | 13150 | 2 | 0 | 1 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0042 | 0/0 | 13155 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0043 | 0/0 | 13152 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0044 | 0/0 | 13148 | 1 | 0 | 0 | 0 | 1 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0045 | 0/0 | 13148 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0046 | 0/0 | 13149 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0047 | 0/0 | 13148 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0048 | 0/0 | 13134 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0049 | 0/0 | 13134 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0050 | 0/0 | 13134 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0051 | 0/0 | 13151 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0052 | 0/0 | 13151 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0053 | 0/0 | 13156 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0054 | 0/0 | 13155 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0055 | 0/0 | 13155 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0056 | 0/0 | 13154 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0057 | 0/0 | 13151 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0058 | 0/0 | 13149 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0059 | 0/0 | 13150 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0060 | 0/0 | 13151 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0061 | 0/0 | 13148 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0062 | 0/0 | 13152 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0063 | 0/0 | 13149 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0064 | 0/0 | 13149 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0065 | 0/0 | 13150 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0066 | 0/0 | 13150 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0067 | 0/0 | 13151 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0068 | 0/0 | 13150 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0069 | 0/0 | 13150 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0070 | 0/0 | 13156 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0071 | 0/0 | 13148 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0072 | 0/0 | 13151 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0073 | 0/0 | 13150 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0074 | 0/0 | 13148 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0075 | 0/0 | 13151 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0076 | 0/0 | 13150 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0077 | 0/0 | 13148 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0078 | 0/0 | 13150 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0079 | 0/0 | 13148 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0080 | 0/0 | 13150 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0081 | 0/0 | 13148 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0082 | 0/0 | 13147 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0083 | 0/0 | 13149 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0084 | 0/0 | 13147 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0085 | 0/0 | 13149 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0086 | 0/0 | 13148 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0087 | 0/0 | 13147 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0088 | 0/0 | 13152 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0089 | 0/0 | 13149 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0090 | 0/0 | 13150 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0091 | 0/0 | 13152 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0092 | 0/0 | 13149 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0093 | 0/0 | 13148 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0094 | 0/0 | 13150 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0095 | 0/0 | 13152 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0096 | 0/0 | 13148 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0097 | 0/0 | 13149 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0098 | 0/0 | 13150 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0099 | 0/0 | 13148 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0100 | 0/0 | 13148 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0101 | 0/0 | 13148 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0102 | 0/0 | 13150 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0103 | 0/0 | 13152 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0104 | 0/0 | 13148 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0105 | 0/0 | 13150 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0106 | 0/0 | 13152 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0107 | 0/0 | 13151 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0108 | 0/0 | 13151 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0109 | 0/0 | 13150 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0110 | 0/0 | 13152 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0111 | 0/0 | 13152 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0112 | 0/0 | 13151 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0113 | 0/0 | 13151 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0114 | 0/0 | 13151 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0115 | 0/0 | 13152 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0116 | 0/0 | 13150 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0117 | 0/0 | 13149 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0118 | 0/0 | 13150 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0119 | 0/0 | 13149 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0120 | 0/0 | 13148 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0121 | 0/0 | 13148 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0122 | 0/0 | 13152 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0123 | 0/0 | 13149 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0124 | 0/0 | 13134 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0125 | 0/0 | 13133 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0126 | 0/0 | 13132 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0127 | 0/0 | 13151 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0128 | 0/0 | 13143 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0129 | 0/0 | 13147 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0130 | 0/0 | 13152 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0131 | 0/0 | 13151 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0132 | 0/0 | 13149 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0133 | 0/0 | 13149 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0134 | 0/0 | 13151 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0135 | 0/0 | 13148 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0136 | 0/0 | 13137 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0137 | 0/0 | 13152 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0138 | 0/0 | 13150 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0139 | 0/0 | 13151 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0140 | 0/0 | 13151 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0141 | 0/0 | 13076 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
t0142 | 0/0 | 13151 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
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 | 8 | 0 | 1 | 7 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0002 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0003 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0004 | 0/0 | 4 | 3 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0005 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0007 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0008 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0014 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0018 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0022 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
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 | 0/0 | 1134 | 159 | 48 | 30 | 57 | 6 | 18 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0002 | 0/0 | 1134 | 103 | 37 | 20 | 34 | 5 | 7 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0003 | 0/0 | 1134 | 81 | 13 | 10 | 52 | 1 | 5 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0004 | 0/0 | 1134 | 2 | 0 | 2 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0002c0005 | 0/0 | 1134 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 14281 | 48 | 2 | 14 | 21 | 4 | 7 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0001t0005 | 0/0 | 14283 | 10 | 0 | 1 | 9 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0001t0007 | 0/0 | 14267 | 8 | 7 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0001t0013 | 0/0 | 14281 | 4 | 0 | 0 | 3 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0001t0014 | 0/0 | 14281 | 4 | 3 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0001t0016 | 0/0 | 14281 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0001t0017 | 0/0 | 14282 | 3 | 0 | 0 | 1 | 0 | 2 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0001t0018 | 0/0 | 14280 | 3 | 0 | 0 | 3 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0001t0023 | 0/0 | 14284 | 3 | 2 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0001t0024 | 0/0 | 14285 | 3 | 2 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0001t0025 | 0/0 | 14282 | 3 | 0 | 3 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0001t0026 | 0/0 | 14285 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0001t0030 | 0/0 | 14284 | 2 | 0 | 0 | 0 | 1 | 1 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0001t0031 | 0/0 | 14284 | 2 | 0 | 0 | 2 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0001t0032 | 0/0 | 14285 | 2 | 1 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0001t0039 | 0/0 | 14282 | 2 | 0 | 1 | 0 | 1 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0001t0040 | 0/0 | 14281 | 2 | 2 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0001t0046 | 0/0 | 14282 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0001t0047 | 0/0 | 14281 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0001t0048 | 0/0 | 14267 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0001t0049 | 0/0 | 14267 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0001t0050 | 0/0 | 14267 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0001t0059 | 0/0 | 14283 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0001t0061 | 0/0 | 14281 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0001t0062 | 0/0 | 14285 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0001t0063 | 0/0 | 14282 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0001t0064 | 0/0 | 14282 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0001t0065 | 0/0 | 14283 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0001t0066 | 0/0 | 14283 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0001t0067 | 0/0 | 14284 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0001t0068 | 0/0 | 14283 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0001t0069 | 0/0 | 14283 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0001t0070 | 0/0 | 14289 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0001t0071 | 0/0 | 14281 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0001t0072 | 0/0 | 14284 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0001t0073 | 0/0 | 14283 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0001t0074 | 0/0 | 14281 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0001t0075 | 0/0 | 14284 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0001t0076 | 0/0 | 14283 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0001t0077 | 0/0 | 14281 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0001t0078 | 0/0 | 14283 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0001t0079 | 0/0 | 14281 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0001t0080 | 0/0 | 14283 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0001t0081 | 0/0 | 14281 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0001t0082 | 0/0 | 14280 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0001t0083 | 0/0 | 14282 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0001t0085 | 0/0 | 14282 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0001t0086 | 0/0 | 14281 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0001t0087 | 0/0 | 14280 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0001t0088 | 0/0 | 14285 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0001t0089 | 0/0 | 14282 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0001t0090 | 0/0 | 14283 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0001t0091 | 0/0 | 14285 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0001t0092 | 0/0 | 14282 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0001t0093 | 0/0 | 14281 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0001t0094 | 0/0 | 14283 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0001t0095 | 0/0 | 14285 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0001t0096 | 0/0 | 14281 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0001t0097 | 0/0 | 14282 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0001t0098 | 0/0 | 14283 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0001t0099 | 0/0 | 14281 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0001t0100 | 0/0 | 14281 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0001t0120 | 0/0 | 14281 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0001t0121 | 0/0 | 14281 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0001t0122 | 0/0 | 14285 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0001t0123 | 0/0 | 14282 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0001t0124 | 0/0 | 14267 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0001t0125 | 0/0 | 14266 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0001t0126 | 0/0 | 14265 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0001t0130 | 0/0 | 14285 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0001t0132 | 0/0 | 14282 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0001t0133 | 0/0 | 14282 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0001t0134 | 0/0 | 14284 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0001t0135 | 0/0 | 14281 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0001t0136 | 0/0 | 14270 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0002t0002 | 0/0 | 14283 | 31 | 0 | 9 | 19 | 1 | 2 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0002t0004 | 0/0 | 14285 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0002t0006 | 0/0 | 14289 | 8 | 8 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0002t0008 | 0/0 | 14281 | 6 | 0 | 1 | 0 | 3 | 2 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0002t0009 | 0/0 | 14282 | 6 | 4 | 2 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0002t0010 | 0/0 | 14284 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0002t0012 | 0/0 | 14290 | 4 | 4 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0002t0015 | 0/0 | 14261 | 3 | 3 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0002t0016 | 0/0 | 14281 | 2 | 0 | 0 | 2 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0002t0019 | 0/0 | 14284 | 2 | 0 | 0 | 2 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0002t0020 | 0/0 | 14283 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0002t0022 | 0/0 | 14284 | 3 | 0 | 0 | 3 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0002t0026 | 0/0 | 14285 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0002t0028 | 0/0 | 14288 | 2 | 2 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0002t0029 | 0/0 | 14276 | 2 | 1 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0002t0033 | 0/0 | 14284 | 2 | 0 | 1 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0002t0036 | 0/0 | 14269 | 2 | 0 | 0 | 2 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0002t0041 | 0/0 | 14283 | 2 | 0 | 1 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0002t0042 | 0/0 | 14288 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0002t0043 | 0/0 | 14285 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0002t0044 | 0/0 | 14281 | 1 | 0 | 0 | 0 | 1 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0002t0045 | 0/0 | 14281 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0002t0051 | 0/0 | 14284 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0002t0052 | 0/0 | 14284 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0002t0053 | 0/0 | 14289 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0002t0054 | 0/0 | 14288 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0002t0055 | 0/0 | 14288 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0002t0056 | 0/0 | 14287 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0002t0057 | 0/0 | 14284 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0002t0058 | 0/0 | 14282 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0002t0084 | 0/0 | 14280 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0002t0102 | 0/0 | 14283 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0002t0116 | 0/0 | 14283 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0002t0117 | 0/0 | 14282 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0002t0119 | 0/0 | 14282 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0002t0127 | 0/0 | 14284 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0002t0128 | 0/0 | 14276 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0002t0129 | 0/0 | 14280 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0002t0131 | 0/0 | 14284 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0002t0140 | 0/0 | 14284 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0002t0141 | 0/0 | 14209 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0002t0142 | 0/0 | 14284 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0003t0002 | 0/0 | 14283 | 2 | 0 | 0 | 2 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0003t0003 | 0/0 | 14284 | 18 | 0 | 1 | 16 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0003t0004 | 0/0 | 14285 | 15 | 8 | 2 | 5 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0003t0010 | 0/0 | 14284 | 5 | 0 | 0 | 5 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0003t0011 | 0/0 | 14284 | 5 | 0 | 0 | 5 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0003t0020 | 0/0 | 14283 | 2 | 2 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0003t0021 | 0/0 | 14285 | 3 | 0 | 0 | 0 | 1 | 2 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0003t0026 | 0/0 | 14285 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0003t0027 | 0/0 | 14284 | 3 | 0 | 0 | 3 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0003t0034 | 0/0 | 14286 | 2 | 0 | 0 | 1 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0003t0035 | 0/0 | 14285 | 2 | 0 | 0 | 1 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0003t0037 | 0/0 | 14286 | 2 | 0 | 0 | 2 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0003t0038 | 0/0 | 14285 | 2 | 0 | 0 | 2 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0003t0060 | 0/0 | 14284 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0003t0101 | 0/0 | 14281 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0003t0103 | 0/0 | 14285 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0003t0104 | 0/0 | 14281 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0003t0105 | 0/0 | 14283 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0003t0106 | 0/0 | 14285 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0003t0107 | 0/0 | 14284 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0003t0108 | 0/0 | 14284 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0003t0109 | 0/0 | 14283 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0003t0110 | 0/0 | 14285 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0003t0111 | 0/0 | 14285 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0003t0112 | 0/0 | 14284 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0003t0113 | 0/0 | 14284 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0003t0114 | 0/0 | 14284 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0003t0115 | 0/0 | 14285 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0003t0118 | 0/0 | 14283 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0003t0137 | 0/0 | 14285 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0003t0138 | 0/0 | 14283 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0003t0139 | 0/0 | 14284 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0001c0004t0001 | 0/0 | 14281 | 2 | 0 | 2 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
a0002c0005t0019 | 0/0 | 14284 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | copy fasta | chr2 | 112477156 | 112546739 |
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 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0005g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0005g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0005g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0005g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0005g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0005g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0005g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0007g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0007g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0007g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0007g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0007g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0007g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0007g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0007g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0013g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0013g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0013g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0013g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0014g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0014g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0014g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0014g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0016g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0017g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0017g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0017g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0018g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0018g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0018g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0023g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0023g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0024g0007 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0025g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0025g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0026g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0030g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0030g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0031g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0031g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0032g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0032g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0039g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0039g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0040g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0040g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0046g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0047g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0048g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0049g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0050g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0059g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0061g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0062g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0063g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0064g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0065g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0066g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0067g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0068g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0069g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0070g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0071g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0072g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0073g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0074g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0075g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0076g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0077g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0078g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0079g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0080g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0081g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0082g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0083g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0085g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0086g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0087g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0088g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0089g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0090g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0091g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0092g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0093g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0094g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0095g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0096g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0097g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0098g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0099g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0100g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0120g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0121g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0122g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0123g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0124g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0125g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0126g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0130g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0132g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0133g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0134g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0135g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0001t0136g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0002g0003 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0002g0008 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0002g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0004g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0006g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0006g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0006g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0006g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0006g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0006g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0006g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0008g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0008g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0008g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0008g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0008g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0008g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0009g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0009g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0009g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0009g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0009g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0009g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0010g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0012g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0012g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0012g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0012g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0015g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0015g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0015g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0016g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0016g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0019g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0019g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0020g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0022g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0022g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0022g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0026g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0028g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0028g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0029g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0029g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0033g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0033g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0036g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0036g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0041g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0041g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0042g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0043g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0044g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0045g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0051g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0052g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0053g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0054g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0055g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0056g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0057g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0058g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0084g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0102g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0116g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0117g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0119g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0127g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0128g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0129g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0131g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0140g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0141g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0002t0142g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0003g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0003g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0003g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0003g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0003g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0003g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0003g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0004g0002 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0004g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0004g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0004g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0004g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0004g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0004g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0004g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0004g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0004g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0004g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0010g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0010g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0010g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0010g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0010g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0011g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0011g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0011g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0011g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0020g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0020g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0021g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0021g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0021g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0026g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0027g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0027g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0034g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0034g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0035g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0035g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0037g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0037g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0038g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0060g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0101g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0103g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0104g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0105g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0106g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0107g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0108g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0109g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0110g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0111g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0112g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0113g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0114g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0115g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0118g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0137g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0138g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0003t0139g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0004t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0001c0004t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
a0002c0005t0019g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0078 | EUR | GBR | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG00099 | hp2 | a0001 | c0002 | t0008 | g0089 | EUR | GBR | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG00140 | hp1 | a0001 | c0002 | t0008 | g0070 | EUR | GBR | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG00140 | hp2 | a0001 | c0001 | t0030 | g0258 | EUR | GBR | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG00280 | hp1 | a0001 | c0003 | t0021 | g0171 | EUR | FIN | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG00280 | hp2 | a0001 | c0002 | t0044 | g0071 | EUR | FIN | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG00408 | hp1 | a0001 | c0003 | t0113 | g0169 | EAS | CHS | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | CHS | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG00423 | hp2 | a0001 | c0003 | t0037 | g0161 | EAS | CHS | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG00438 | hp1 | a0001 | c0002 | t0036 | g0301 | EAS | CHS | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG00438 | hp2 | a0001 | c0001 | t0031 | g0267 | EAS | CHS | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG00544 | hp1 | a0001 | c0001 | t0083 | g0005 | EAS | CHS | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG00544 | hp2 | a0001 | c0003 | t0037 | g0157 | EAS | CHS | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG00621 | hp1 | a0001 | c0002 | t0002 | g0134 | EAS | CHS | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG00621 | hp2 | a0001 | c0003 | t0004 | g0002 | EAS | CHS | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG00639 | hp1 | a0001 | c0001 | t0007 | g0054 | AMR | PUR | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG00639 | hp2 | a0001 | c0003 | t0107 | g0173 | AMR | PUR | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG00673 | hp1 | a0002 | c0005 | t0019 | g0137 | EAS | CHS | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG00735 | hp1 | a0001 | c0003 | t0112 | g0149 | AMR | PUR | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG00735 | hp2 | a0001 | c0002 | t0002 | g0118 | AMR | PUR | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG00738 | hp1 | a0001 | c0003 | t0004 | g0002 | AMR | PUR | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG00738 | hp2 | a0001 | c0001 | t0025 | g0042 | AMR | PUR | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0304 | AMR | PUR | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG00741 | hp2 | a0001 | c0003 | t0004 | g0284 | AMR | PUR | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01070 | hp2 | a0001 | c0002 | t0002 | g0182 | AMR | PUR | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01071 | hp1 | a0001 | c0002 | t0002 | g0008 | AMR | PUR | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01074 | hp1 | a0001 | c0003 | t0105 | g0147 | AMR | PUR | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01074 | hp2 | a0001 | c0002 | t0041 | g0058 | AMR | PUR | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01081 | hp1 | a0001 | c0002 | t0026 | g0059 | AMR | PUR | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01081 | hp2 | a0001 | c0002 | t0002 | g0008 | AMR | PUR | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01106 | hp1 | a0001 | c0003 | t0003 | g0174 | AMR | PUR | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01109 | hp1 | a0001 | c0001 | t0014 | g0044 | AMR | PUR | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | PUR | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01167 | hp1 | a0001 | c0002 | t0004 | g0133 | AMR | PUR | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01167 | hp2 | a0001 | c0001 | t0024 | g0007 | AMR | PUR | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01168 | hp1 | a0001 | c0003 | t0118 | g0155 | AMR | PUR | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01168 | hp2 | a0001 | c0002 | t0084 | g0120 | AMR | PUR | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01175 | hp1 | a0001 | c0001 | t0032 | g0192 | AMR | PUR | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0271 | AMR | PUR | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01243 | hp1 | a0001 | c0001 | t0023 | g0101 | AMR | PUR | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01243 | hp2 | a0001 | c0002 | t0029 | g0188 | AMR | PUR | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | CLM | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01256 | hp2 | a0001 | c0001 | t0025 | g0009 | AMR | CLM | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01257 | hp1 | a0001 | c0002 | t0009 | g0294 | AMR | CLM | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0261 | AMR | CLM | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01258 | hp1 | a0001 | c0002 | t0009 | g0295 | AMR | CLM | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01258 | hp2 | a0001 | c0001 | t0025 | g0009 | AMR | CLM | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01261 | hp1 | a0001 | c0002 | t0117 | g0003 | AMR | CLM | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01261 | hp2 | a0001 | c0003 | t0109 | g0175 | AMR | CLM | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01346 | hp1 | a0001 | c0001 | t0048 | g0275 | AMR | CLM | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | CLM | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01358 | hp1 | a0001 | c0002 | t0043 | g0073 | AMR | CLM | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01358 | hp2 | a0001 | c0001 | t0065 | g0264 | AMR | CLM | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01361 | hp1 | a0001 | c0002 | t0033 | g0130 | AMR | CLM | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01361 | hp2 | a0001 | c0001 | t0091 | g0219 | AMR | CLM | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01496 | hp1 | a0001 | c0004 | t0001 | g0249 | AMR | CLM | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01496 | hp2 | a0001 | c0001 | t0075 | g0220 | AMR | CLM | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01516 | hp1 | a0001 | c0002 | t0008 | g0076 | EUR | IBS | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0087 | EUR | IBS | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01884 | hp1 | a0001 | c0001 | t0132 | g0305 | AFR | ACB | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01884 | hp2 | a0001 | c0002 | t0009 | g0144 | AFR | ACB | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01891 | hp1 | a0001 | c0002 | t0028 | g0097 | AFR | ACB | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01891 | hp2 | a0001 | c0001 | t0040 | g0050 | AFR | ACB | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0270 | AMR | PEL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01928 | hp2 | a0001 | c0004 | t0001 | g0248 | AMR | PEL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01952 | hp1 | a0001 | c0002 | t0002 | g0281 | AMR | PEL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01952 | hp2 | a0001 | c0001 | t0094 | g0001 | AMR | PEL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01975 | hp1 | a0001 | c0003 | t0101 | g0158 | AMR | PEL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01975 | hp2 | a0001 | c0002 | t0002 | g0116 | AMR | PEL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01978 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | PEL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01978 | hp2 | a0001 | c0001 | t0095 | g0225 | AMR | PEL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01981 | hp1 | a0001 | c0003 | t0111 | g0154 | AMR | PEL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01981 | hp2 | a0001 | c0001 | t0039 | g0028 | AMR | PEL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PEL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02004 | hp1 | a0001 | c0001 | t0005 | g0215 | AMR | PEL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02004 | hp2 | a0001 | c0002 | t0002 | g0008 | AMR | PEL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02040 | hp1 | a0001 | c0002 | t0002 | g0181 | EAS | KHV | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02040 | hp2 | a0001 | c0001 | t0018 | g0214 | EAS | KHV | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02055 | hp1 | a0001 | c0001 | t0014 | g0033 | AFR | ACB | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02055 | hp2 | a0001 | c0003 | t0110 | g0241 | AFR | ACB | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02071 | hp1 | a0001 | c0001 | t0005 | g0287 | EAS | KHV | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02071 | hp2 | a0001 | c0002 | t0002 | g0128 | EAS | KHV | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02080 | hp1 | a0001 | c0003 | t0104 | g0163 | EAS | KHV | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02080 | hp2 | a0001 | c0001 | t0013 | g0047 | EAS | KHV | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02083 | hp1 | a0001 | c0003 | t0003 | g0242 | EAS | KHV | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02083 | hp2 | a0001 | c0001 | t0072 | g0253 | EAS | KHV | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02129 | hp1 | a0001 | c0003 | t0034 | g0232 | EAS | KHV | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | KHV | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | KHV | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02132 | hp2 | a0001 | c0002 | t0002 | g0080 | EAS | KHV | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02135 | hp1 | a0001 | c0002 | t0141 | g0283 | EAS | KHV | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02135 | hp2 | a0001 | c0003 | t0003 | g0286 | EAS | KHV | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02145 | hp1 | a0001 | c0002 | t0057 | g0280 | AFR | ACB | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | ACB | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | CDX | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02155 | hp2 | a0001 | c0003 | t0010 | g0062 | EAS | CDX | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CDX | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02165 | hp2 | a0001 | c0002 | t0140 | g0045 | EAS | CDX | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02257 | hp1 | a0001 | c0001 | t0100 | g0103 | AFR | ACB | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02257 | hp2 | a0001 | c0001 | t0086 | g0114 | AFR | ACB | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02258 | hp1 | a0001 | c0001 | t0007 | g0038 | AFR | ACB | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02258 | hp2 | a0001 | c0001 | t0133 | g0043 | AFR | ACB | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02280 | hp1 | a0001 | c0002 | t0009 | g0297 | AFR | ACB | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02280 | hp2 | a0001 | c0003 | t0137 | g0026 | AFR | ACB | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02293 | hp1 | a0001 | c0002 | t0008 | g0075 | AMR | PEL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | PEL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02300 | hp1 | a0001 | c0002 | t0002 | g0122 | AMR | PEL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02451 | hp1 | a0001 | c0001 | t0130 | g0041 | AFR | ACB | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02451 | hp2 | a0001 | c0002 | t0058 | g0096 | AFR | ACB | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02523 | hp1 | a0001 | c0001 | t0013 | g0049 | EAS | KHV | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02523 | hp2 | a0001 | c0003 | t0004 | g0176 | EAS | KHV | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | GWD | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02572 | hp2 | a0001 | c0002 | t0006 | g0110 | AFR | GWD | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02602 | hp1 | a0001 | c0001 | t0017 | g0268 | SAS | PJL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02602 | hp2 | a0001 | c0001 | t0135 | g0024 | SAS | PJL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02615 | hp1 | a0001 | c0003 | t0004 | g0004 | AFR | GWD | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02615 | hp2 | a0001 | c0002 | t0012 | g0105 | AFR | GWD | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02622 | hp1 | a0001 | c0002 | t0006 | g0012 | AFR | GWD | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02622 | hp2 | a0001 | c0001 | t0071 | g0099 | AFR | GWD | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02630 | hp1 | a0001 | c0003 | t0004 | g0004 | AFR | GWD | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02630 | hp2 | a0001 | c0001 | t0097 | g0211 | AFR | GWD | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02647 | hp1 | a0001 | c0002 | t0055 | g0279 | AFR | GWD | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02647 | hp2 | a0001 | c0002 | t0127 | g0039 | AFR | GWD | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02683 | hp1 | a0001 | c0002 | t0119 | g0238 | SAS | PJL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02683 | hp2 | a0001 | c0001 | t0099 | g0256 | SAS | PJL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02698 | hp2 | a0001 | c0002 | t0008 | g0072 | SAS | PJL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02717 | hp1 | a0001 | c0001 | t0136 | g0032 | AFR | GWD | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02717 | hp2 | a0001 | c0001 | t0007 | g0055 | AFR | GWD | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02723 | hp1 | a0001 | c0002 | t0129 | g0069 | AFR | GWD | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02723 | hp2 | a0001 | c0001 | t0122 | g0102 | AFR | GWD | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02738 | hp1 | a0001 | c0001 | t0093 | g0240 | SAS | PJL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02738 | hp2 | a0001 | c0001 | t0017 | g0250 | SAS | PJL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02809 | hp1 | a0001 | c0001 | t0069 | g0212 | AFR | GWD | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02809 | hp2 | a0001 | c0002 | t0012 | g0109 | AFR | GWD | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02818 | hp1 | a0001 | c0002 | t0012 | g0111 | AFR | GWD | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02818 | hp2 | a0001 | c0001 | t0046 | g0195 | AFR | GWD | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02886 | hp1 | a0001 | c0001 | t0007 | g0037 | AFR | GWD | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02886 | hp2 | a0001 | c0003 | t0020 | g0115 | AFR | GWD | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02895 | hp1 | a0001 | c0002 | t0054 | g0234 | AFR | GWD | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02895 | hp2 | a0001 | c0002 | t0128 | g0040 | AFR | GWD | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02896 | hp1 | a0001 | c0002 | t0052 | g0236 | AFR | GWD | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02896 | hp2 | a0001 | c0001 | t0007 | g0053 | AFR | GWD | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02897 | hp1 | a0001 | c0002 | t0053 | g0233 | AFR | GWD | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02897 | hp2 | a0001 | c0001 | t0007 | g0052 | AFR | GWD | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02922 | hp1 | a0001 | c0001 | t0076 | g0090 | AFR | ESN | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02922 | hp2 | a0001 | c0002 | t0051 | g0237 | AFR | ESN | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02965 | hp1 | a0001 | c0001 | t0126 | g0035 | AFR | ESN | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02965 | hp2 | a0001 | c0002 | t0006 | g0107 | AFR | ESN | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02970 | hp1 | a0001 | c0001 | t0120 | g0100 | AFR | ESN | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02970 | hp2 | a0001 | c0002 | t0006 | g0106 | AFR | ESN | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02976 | hp1 | a0001 | c0001 | t0032 | g0193 | AFR | ESN | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02976 | hp2 | a0001 | c0001 | t0089 | g0206 | AFR | ESN | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG03017 | hp1 | a0001 | c0001 | t0081 | g0005 | SAS | PJL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG03017 | hp2 | a0001 | c0002 | t0008 | g0074 | SAS | PJL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG03041 | hp1 | a0001 | c0001 | t0007 | g0051 | AFR | GWD | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG03041 | hp2 | a0001 | c0001 | t0014 | g0031 | AFR | GWD | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG03098 | hp1 | a0001 | c0002 | t0006 | g0104 | AFR | MSL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG03098 | hp2 | a0001 | c0002 | t0142 | g0095 | AFR | MSL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG03130 | hp1 | a0001 | c0003 | t0004 | g0168 | AFR | ESN | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG03130 | hp2 | a0001 | c0001 | t0024 | g0007 | AFR | ESN | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG03139 | hp1 | a0001 | c0001 | t0079 | g0257 | AFR | ESN | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG03139 | hp2 | a0001 | c0002 | t0009 | g0296 | AFR | ESN | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG03195 | hp1 | a0001 | c0002 | t0015 | g0083 | AFR | ESN | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG03195 | hp2 | a0001 | c0001 | t0040 | g0046 | AFR | ESN | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG03209 | hp1 | a0001 | c0002 | t0045 | g0081 | AFR | MSL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG03209 | hp2 | a0001 | c0002 | t0006 | g0012 | AFR | MSL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG03225 | hp1 | a0001 | c0002 | t0012 | g0112 | AFR | MSL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG03225 | hp2 | a0001 | c0003 | t0004 | g0150 | AFR | MSL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG03239 | hp1 | a0001 | c0003 | t0021 | g0165 | SAS | PJL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG03453 | hp1 | a0001 | c0003 | t0020 | g0177 | AFR | MSL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG03453 | hp2 | a0001 | c0002 | t0028 | g0146 | AFR | MSL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG03490 | hp1 | a0001 | c0001 | t0030 | g0244 | SAS | PJL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG03490 | hp2 | a0001 | c0001 | t0134 | g0029 | SAS | PJL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG03516 | hp1 | a0001 | c0002 | t0015 | g0084 | AFR | ESN | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG03516 | hp2 | a0001 | c0002 | t0056 | g0094 | AFR | ESN | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG03540 | hp1 | a0001 | c0001 | t0077 | g0292 | AFR | GWD | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG03540 | hp2 | a0001 | c0002 | t0020 | g0093 | AFR | GWD | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG03579 | hp1 | a0001 | c0003 | t0004 | g0153 | AFR | MSL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG03579 | hp2 | a0001 | c0002 | t0131 | g0034 | AFR | MSL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG03704 | hp1 | a0001 | c0001 | t0098 | g0277 | SAS | PJL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0274 | SAS | PJL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0252 | SAS | PJL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG03710 | hp2 | a0001 | c0002 | t0002 | g0136 | SAS | PJL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG03927 | hp1 | a0001 | c0002 | t0116 | g0289 | SAS | BEB | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG03927 | hp2 | a0001 | c0002 | t0042 | g0088 | SAS | BEB | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG03942 | hp1 | a0001 | c0003 | t0021 | g0152 | SAS | BEB | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | BEB | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG04115 | hp1 | a0001 | c0001 | t0013 | g0048 | SAS | STU | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG04115 | hp2 | a0001 | c0003 | t0035 | g0156 | SAS | STU | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG04184 | hp1 | a0001 | c0003 | t0034 | g0180 | SAS | BEB | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0251 | SAS | BEB | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG04199 | hp1 | a0001 | c0001 | t0121 | g0262 | SAS | STU | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG04199 | hp2 | a0001 | c0002 | t0002 | g0135 | SAS | STU | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG04204 | hp1 | a0001 | c0003 | t0003 | g0159 | SAS | STU | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0278 | SAS | STU | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18522 | hp1 | a0001 | c0003 | t0004 | g0148 | AFR | YRI | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18522 | hp2 | a0001 | c0002 | t0009 | g0143 | AFR | YRI | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CHB | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18612 | hp2 | a0001 | c0003 | t0035 | g0243 | EAS | CHB | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18906 | hp1 | a0001 | c0001 | t0125 | g0036 | AFR | YRI | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18906 | hp2 | a0001 | c0001 | t0124 | g0067 | AFR | YRI | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18939 | hp1 | a0001 | c0002 | t0002 | g0129 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18939 | hp2 | a0001 | c0001 | t0082 | g0259 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18942 | hp1 | a0001 | c0001 | t0087 | g0190 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18942 | hp2 | a0001 | c0003 | t0003 | g0160 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18943 | hp2 | a0001 | c0002 | t0016 | g0123 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18944 | hp2 | a0001 | c0003 | t0003 | g0015 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18945 | hp1 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18945 | hp2 | a0001 | c0003 | t0003 | g0230 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18947 | hp1 | a0001 | c0002 | t0002 | g0132 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18948 | hp1 | a0001 | c0003 | t0011 | g0228 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18948 | hp2 | a0001 | c0003 | t0003 | g0299 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18950 | hp1 | a0001 | c0001 | t0062 | g0213 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18954 | hp1 | a0001 | c0003 | t0038 | g0002 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18954 | hp2 | a0001 | c0001 | t0092 | g0199 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18957 | hp1 | a0001 | c0003 | t0026 | g0010 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18957 | hp2 | a0001 | c0001 | t0067 | g0207 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18960 | hp1 | a0001 | c0001 | t0074 | g0266 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18960 | hp2 | a0001 | c0003 | t0011 | g0023 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18961 | hp1 | a0001 | c0003 | t0003 | g0303 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18961 | hp2 | a0001 | c0002 | t0041 | g0060 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18963 | hp1 | a0001 | c0003 | t0010 | g0064 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18963 | hp2 | a0001 | c0002 | t0036 | g0302 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18964 | hp1 | a0001 | c0002 | t0022 | g0126 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18964 | hp2 | a0001 | c0003 | t0011 | g0023 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18965 | hp1 | a0001 | c0002 | t0033 | g0282 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18968 | hp1 | a0001 | c0001 | t0064 | g0017 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18968 | hp2 | a0001 | c0003 | t0003 | g0004 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18970 | hp2 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18971 | hp2 | a0001 | c0003 | t0027 | g0006 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18973 | hp1 | a0001 | c0003 | t0002 | g0170 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18973 | hp2 | a0001 | c0002 | t0010 | g0057 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18974 | hp1 | a0001 | c0002 | t0019 | g0117 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18974 | hp2 | a0001 | c0003 | t0003 | g0229 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18979 | hp1 | a0001 | c0002 | t0019 | g0014 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18979 | hp2 | a0001 | c0003 | t0106 | g0231 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18980 | hp1 | a0001 | c0003 | t0027 | g0006 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18980 | hp2 | a0001 | c0002 | t0002 | g0131 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18981 | hp1 | a0001 | c0002 | t0002 | g0186 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18981 | hp2 | a0001 | c0001 | t0073 | g0020 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18985 | hp1 | a0001 | c0003 | t0027 | g0061 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18985 | hp2 | a0001 | c0001 | t0068 | g0198 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18986 | hp1 | a0001 | c0003 | t0003 | g0183 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18986 | hp2 | a0001 | c0002 | t0002 | g0121 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18989 | hp1 | a0001 | c0001 | t0031 | g0290 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18989 | hp2 | a0001 | c0003 | t0002 | g0172 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18992 | hp1 | a0001 | c0002 | t0002 | g0140 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18992 | hp2 | a0001 | c0001 | t0078 | g0001 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18994 | hp1 | a0001 | c0003 | t0010 | g0066 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18994 | hp2 | a0001 | c0001 | t0005 | g0217 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18995 | hp1 | a0001 | c0003 | t0103 | g0167 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18995 | hp2 | a0001 | c0001 | t0063 | g0209 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18998 | hp1 | a0001 | c0003 | t0003 | g0226 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18998 | hp2 | a0001 | c0001 | t0018 | g0288 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18999 | hp1 | a0001 | c0001 | t0013 | g0063 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA18999 | hp2 | a0001 | c0003 | t0003 | g0239 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19001 | hp1 | a0001 | c0002 | t0022 | g0125 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19001 | hp2 | a0001 | c0001 | t0066 | g0200 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19002 | hp1 | a0001 | c0001 | t0059 | g0001 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19002 | hp2 | a0001 | c0002 | t0002 | g0185 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19003 | hp1 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19003 | hp2 | a0001 | c0003 | t0115 | g0178 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19004 | hp2 | a0001 | c0003 | t0038 | g0002 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19005 | hp1 | a0001 | c0001 | t0080 | g0020 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19005 | hp2 | a0001 | c0002 | t0102 | g0003 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19009 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19009 | hp2 | a0001 | c0003 | t0003 | g0227 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19011 | hp1 | a0001 | c0003 | t0004 | g0002 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19011 | hp2 | a0001 | c0001 | t0061 | g0218 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19030 | hp1 | a0001 | c0001 | t0049 | g0291 | AFR | LWK | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19030 | hp2 | a0001 | c0001 | t0088 | g0086 | AFR | LWK | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19043 | hp1 | a0001 | c0001 | t0014 | g0030 | AFR | LWK | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19043 | hp2 | a0001 | c0001 | t0007 | g0068 | AFR | LWK | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19054 | hp1 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19054 | hp2 | a0001 | c0002 | t0002 | g0013 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19056 | hp1 | a0001 | c0001 | t0005 | g0221 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19056 | hp2 | a0001 | c0003 | t0003 | g0164 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19057 | hp1 | a0001 | c0002 | t0002 | g0138 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19057 | hp2 | a0001 | c0003 | t0010 | g0065 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19060 | hp1 | a0001 | c0003 | t0011 | g0298 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19060 | hp2 | a0001 | c0001 | t0005 | g0223 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19065 | hp1 | a0001 | c0002 | t0002 | g0013 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19066 | hp1 | a0001 | c0001 | t0018 | g0224 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19066 | hp2 | a0001 | c0003 | t0003 | g0151 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19072 | hp1 | a0001 | c0003 | t0060 | g0179 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19072 | hp2 | a0001 | c0001 | t0016 | g0194 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19075 | hp1 | a0001 | c0002 | t0002 | g0124 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19075 | hp2 | a0001 | c0003 | t0004 | g0184 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19077 | hp1 | a0001 | c0002 | t0002 | g0119 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19077 | hp2 | a0001 | c0003 | t0108 | g0285 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19079 | hp1 | a0001 | c0003 | t0010 | g0010 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19079 | hp2 | a0001 | c0002 | t0016 | g0127 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19080 | hp1 | a0001 | c0002 | t0002 | g0189 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19081 | hp1 | a0001 | c0001 | t0017 | g0204 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19081 | hp2 | a0001 | c0003 | t0004 | g0113 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19084 | hp2 | a0001 | c0003 | t0011 | g0300 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19087 | hp1 | a0001 | c0002 | t0022 | g0139 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19088 | hp1 | a0001 | c0003 | t0003 | g0015 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19090 | hp1 | a0001 | c0002 | t0002 | g0079 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19090 | hp2 | a0001 | c0003 | t0139 | g0006 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19091 | hp1 | a0001 | c0003 | t0114 | g0166 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19091 | hp2 | a0001 | c0001 | t0005 | g0216 | EAS | JPT | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19240 | hp1 | a0001 | c0001 | t0070 | g0082 | AFR | YRI | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA19240 | hp2 | a0001 | c0001 | t0090 | g0293 | AFR | YRI | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA20129 | hp1 | a0001 | c0002 | t0006 | g0235 | AFR | ASW | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA20129 | hp2 | a0001 | c0001 | t0024 | g0007 | AFR | ASW | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0092 | EUR | TSI | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA20752 | hp2 | a0001 | c0001 | t0039 | g0027 | EUR | TSI | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA20805 | hp1 | a0001 | c0002 | t0002 | g0014 | EUR | TSI | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0255 | EUR | TSI | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02109 | hp1 | a0001 | c0001 | t0123 | g0098 | AFR | ACB | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02109 | hp2 | a0001 | c0002 | t0015 | g0085 | AFR | ACB | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02486 | hp1 | a0001 | c0001 | t0050 | g0276 | AFR | ACB | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02486 | hp2 | a0001 | c0001 | t0023 | g0011 | AFR | ACB | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02559 | hp1 | a0001 | c0001 | t0026 | g0056 | AFR | ACB | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG02559 | hp2 | a0001 | c0001 | t0023 | g0011 | AFR | ACB | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG03471 | hp1 | a0001 | c0001 | t0047 | g0141 | AFR | MSL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG03471 | hp2 | a0001 | c0003 | t0004 | g0004 | AFR | MSL | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG06807 | hp1 | a0001 | c0002 | t0006 | g0108 | AFR | USA | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
HG06807 | hp2 | a0001 | c0003 | t0004 | g0162 | AFR | USA | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA20300 | hp1 | a0001 | c0002 | t0029 | g0187 | AFR | USA | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA20300 | hp2 | a0001 | c0001 | t0085 | g0145 | AFR | USA | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA21309 | hp1 | a0001 | c0003 | t0138 | g0025 | AFR | LWK | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
NA21309 | hp2 | a0001 | c0001 | t0096 | g0091 | AFR | LWK | TTL_chr2_112477156_112546739 | TTL | chr2 | 112477156 | 112546739 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:112485925
|
C | T | 1 | a0002 | 1 | HG00673.hp1 | missense_variant | MODERATE | c.166C>T | p.Pro56Ser | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/7 | 355/14267 | 166/1134 | 56/377 | chr2 | 112485925 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:112494341
|
C | T | 1 | a0001c0004 | 2 | HG01496.hp1 HG01928.hp2 |
synonymous_variant | LOW | c.435C>T | p.Asn145Asn | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/7 | 624/14267 | 435/1134 | 145/377 | chr2 | 112494341 | ||
chr2:112501339
|
C | T | 3 | a0001c0002a0001c0003a0002c0005 | 185 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(182): Show |
splice_region_variant&synonymous_variant | LOW | c.603C>T | p.Ile201Ile | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 4/7 | 792/14267 | 603/1134 | 201/377 | chr2 | 112501339 | ||
chr2:112520372
|
T | C | 1 | a0001c0003 | 81 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(78): Show |
synonymous_variant | LOW | c.966T>C | p.Asp322Asp | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/7 | 1155/14267 | 966/1134 | 322/377 | chr2 | 112520372 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:112482172
|
C | G | 1 | a0001c0002t0142 | 1 | HG03098.hp2 | 5_prime_UTR_variant | MODIFIER | c.-173C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 1/7 | 173 | chr2 | 112482172 | |||||
chr2:112482173
|
CCGGCGGG others(68): Show |
C | 1 | a0001c0002t0141 | 1 | HG02135.hp1 | 5_prime_UTR_variant | MODIFIER | c.-154_-80delCGGCGCC others(68): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 1/7 | 80 | INFO_REALIGN_3_PRIME | chr2 | 112482173 | ||||
chr2:112482234
|
G | T | 1 | a0001c0003t0027 | 3 | NA18971.hp2 NA18980.hp1 NA18985.hp1 |
5_prime_UTR_variant | MODIFIER | c.-111G>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 1/7 | 111 | chr2 | 112482234 | |||||
chr2:112482256
|
C | T | 30 | a0001c0001t0007a0001c0001t0013a0001c0001t0014others(27): Show | 54 | HG00639.hp1 HG00738.hp2 HG01074.hp2 others(51): Show |
5_prime_UTR_variant | MODIFIER | c.-89C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 1/7 | 89 | chr2 | 112482256 | |||||
chr2:112528915
|
T | A | 5 | a0001c0002t0008a0001c0002t0042a0001c0002t0043others(2): Show | 10 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*120T>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 120 | chr2 | 112528915 | |||||
chr2:112528932
|
C | T | 4 | a0001c0001t0023a0001c0001t0024a0001c0001t0122others(1): Show | 8 | HG01167.hp2 HG01243.hp1 HG02109.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*137C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 137 | chr2 | 112528932 | |||||
chr2:112528933
|
G | A | 2 | a0001c0001t0046a0001c0001t0047 | 2 | HG02818.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*138G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 138 | chr2 | 112528933 | |||||
chr2:112528985
|
A | G | 143 | a0001c0001t0001a0001c0001t0005a0001c0001t0013others(140): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
3_prime_UTR_variant | MODIFIER | c.*190A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 190 | chr2 | 112528985 | |||||
chr2:112529074
|
C | T | 1 | a0001c0001t0121 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*279C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 279 | chr2 | 112529074 | |||||
chr2:112529080
|
C | T | 4 | a0001c0001t0023a0001c0001t0024a0001c0001t0122others(1): Show | 8 | HG01167.hp2 HG01243.hp1 HG02109.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*285C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 285 | chr2 | 112529080 | |||||
chr2:112529182
|
G | A | 1 | a0001c0002t0042 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*387G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 387 | chr2 | 112529182 | |||||
chr2:112529337
|
C | T | 1 | a0001c0002t0042 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*542C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 542 | chr2 | 112529337 | |||||
chr2:112529386
|
C | A | 4 | a0001c0001t0023a0001c0001t0024a0001c0001t0122others(1): Show | 8 | HG01167.hp2 HG01243.hp1 HG02109.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*591C>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 591 | chr2 | 112529386 | |||||
chr2:112529622
|
T | A | 2 | a0001c0002t0051a0001c0002t0052 | 2 | HG02896.hp1 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*827T>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 827 | chr2 | 112529622 | |||||
chr2:112529741
|
T | C | 2 | a0001c0001t0016a0001c0002t0016 | 3 | NA18943.hp2 NA19072.hp2 NA19079.hp2 |
3_prime_UTR_variant | MODIFIER | c.*946T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 946 | chr2 | 112529741 | |||||
chr2:112529752
|
C | G | 125 | a0001c0001t0001a0001c0001t0005a0001c0001t0013others(122): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
3_prime_UTR_variant | MODIFIER | c.*957C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 957 | chr2 | 112529752 | |||||
chr2:112530117
|
C | T | 1 | a0001c0001t0120 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1322C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 1322 | chr2 | 112530117 | |||||
chr2:112530153
|
A | G | 4 | a0001c0002t0042a0001c0002t0051a0001c0002t0052others(1): Show | 4 | HG02896.hp1 HG02922.hp2 HG03098.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1358A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 1358 | chr2 | 112530153 | |||||
chr2:112530387
|
A | G | 122 | a0001c0001t0001a0001c0001t0005a0001c0001t0013others(119): Show | 286 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(283): Show |
3_prime_UTR_variant | MODIFIER | c.*1592A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 1592 | chr2 | 112530387 | |||||
chr2:112530436
|
T | C | 1 | a0001c0001t0059 | 1 | NA19002.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1641T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 1641 | chr2 | 112530436 | |||||
chr2:112530608
|
G | A | 1 | a0001c0003t0060 | 1 | NA19072.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1813G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 1813 | chr2 | 112530608 | |||||
chr2:112531003
|
G | A | 143 | a0001c0001t0001a0001c0001t0005a0001c0001t0013others(140): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
3_prime_UTR_variant | MODIFIER | c.*2208G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 2208 | chr2 | 112531003 | |||||
chr2:112531011
|
C | T | 53 | a0001c0001t0014a0001c0001t0026a0001c0001t0100others(50): Show | 141 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(138): Show |
3_prime_UTR_variant | MODIFIER | c.*2216C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 2216 | chr2 | 112531011 | |||||
chr2:112531064
|
C | T | 2 | a0001c0001t0098a0001c0001t0099 | 2 | HG02683.hp2 HG03704.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2269C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 2269 | chr2 | 112531064 | |||||
chr2:112531065
|
G | A | 1 | a0001c0002t0051 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2270G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 2270 | chr2 | 112531065 | |||||
chr2:112531132
|
A | G | 5 | a0001c0001t0032a0001c0001t0040a0001c0001t0096others(2): Show | 7 | HG01175.hp1 HG01891.hp2 HG02109.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2337A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 2337 | chr2 | 112531132 | |||||
chr2:112531200
|
T | C | 1 | a0001c0002t0015 | 3 | HG02109.hp2 HG03195.hp1 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2405T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 2405 | chr2 | 112531200 | |||||
chr2:112531364
|
C | G | 1 | a0001c0002t0140 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2569C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 2569 | chr2 | 112531364 | |||||
chr2:112531455
|
A | G | 51 | a0001c0001t0026a0001c0001t0032a0001c0001t0095others(48): Show | 137 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(134): Show |
3_prime_UTR_variant | MODIFIER | c.*2660A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 2660 | chr2 | 112531455 | |||||
chr2:112531645
|
A | AC | 2 | a0001c0001t0024a0001c0001t0122 | 4 | HG01167.hp2 HG02723.hp2 HG03130.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2850_*2851insC | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 2851 | chr2 | 112531645 | |||||
chr2:112531681
|
A | G | 1 | a0001c0002t0142 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2886A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 2886 | chr2 | 112531681 | |||||
chr2:112531893
|
A | C | 1 | a0001c0001t0094 | 1 | HG01952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3098A>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 3098 | chr2 | 112531893 | |||||
chr2:112532124
|
T | G | 126 | a0001c0001t0001a0001c0001t0005a0001c0001t0013others(123): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
3_prime_UTR_variant | MODIFIER | c.*3329T>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 3329 | chr2 | 112532124 | |||||
chr2:112532623
|
A | T | 1 | a0001c0001t0093 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3828A>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 3828 | chr2 | 112532623 | |||||
chr2:112532630
|
A | C | 1 | a0001c0002t0142 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3835A>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 3835 | chr2 | 112532630 | |||||
chr2:112532658
|
G | A | 1 | a0001c0002t0042 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3863G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 3863 | chr2 | 112532658 | |||||
chr2:112532737
|
T | G | 142 | a0001c0001t0001a0001c0001t0005a0001c0001t0013others(139): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
3_prime_UTR_variant | MODIFIER | c.*3942T>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 3942 | chr2 | 112532737 | |||||
chr2:112532765
|
C | CTCTTAAA others(14): Show |
142 | a0001c0001t0001a0001c0001t0005a0001c0001t0013others(139): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
3_prime_UTR_variant | MODIFIER | c.*3975_*3976insAAAA others(17): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 3976 | INFO_REALIGN_3_PRIME | chr2 | 112532765 | ||||
chr2:112532824
|
G | T | 1 | a0001c0002t0142 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4029G>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 4029 | chr2 | 112532824 | |||||
chr2:112532869
|
T | C | 1 | a0001c0002t0102 | 1 | NA19005.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4074T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 4074 | chr2 | 112532869 | |||||
chr2:112533153
|
A | C | 2 | a0001c0002t0006a0001c0002t0012 | 12 | HG02572.hp2 HG02615.hp2 HG02622.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*4358A>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 4358 | chr2 | 112533153 | |||||
chr2:112533207
|
C | T | 4 | a0001c0002t0008a0001c0002t0043a0001c0002t0044others(1): Show | 9 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4412C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 4412 | chr2 | 112533207 | |||||
chr2:112533301
|
A | T | 4 | a0001c0002t0008a0001c0002t0043a0001c0002t0044others(1): Show | 9 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4506A>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 4506 | chr2 | 112533301 | |||||
chr2:112533412
|
T | G | 1 | a0001c0003t0103 | 1 | NA18995.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4617T>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 4617 | chr2 | 112533412 | |||||
chr2:112533630
|
G | C | 2 | a0001c0002t0051a0001c0002t0052 | 2 | HG02896.hp1 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4835G>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 4835 | chr2 | 112533630 | |||||
chr2:112533808
|
G | A | 50 | a0001c0001t0026a0001c0001t0032a0001c0002t0002others(47): Show | 136 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*5013G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 5013 | chr2 | 112533808 | |||||
chr2:112533896
|
T | C | 1 | a0001c0001t0061 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5101T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 5101 | chr2 | 112533896 | |||||
chr2:112534102
|
C | T | 124 | a0001c0001t0001a0001c0001t0005a0001c0001t0013others(121): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
3_prime_UTR_variant | MODIFIER | c.*5307C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 5307 | chr2 | 112534102 | |||||
chr2:112534109
|
A | G | 1 | a0001c0002t0042 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5314A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 5314 | chr2 | 112534109 | |||||
chr2:112534182
|
C | T | 1 | a0001c0002t0042 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5387C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 5387 | chr2 | 112534182 | |||||
chr2:112534189
|
A | G | 6 | a0001c0002t0009a0001c0002t0029a0001c0002t0058others(3): Show | 12 | HG01243.hp2 HG01257.hp1 HG01258.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*5394A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 5394 | chr2 | 112534189 | |||||
chr2:112534209
|
A | G | 1 | a0001c0003t0038 | 2 | NA18954.hp1 NA19004.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5414A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 5414 | chr2 | 112534209 | |||||
chr2:112534277
|
G | A | 2 | a0001c0001t0014a0001c0001t0100 | 5 | HG01109.hp1 HG02055.hp1 HG02257.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5482G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 5482 | chr2 | 112534277 | |||||
chr2:112534323
|
CAA | C | 10 | a0001c0001t0062a0001c0001t0063a0001c0001t0064others(7): Show | 13 | HG01358.hp2 HG01361.hp1 HG02129.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*5549_*5550delAA | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 5549 | INFO_REALIGN_3_PRIME | chr2 | 112534323 | ||||
chr2:112534323
|
CAAA | C | 114 | a0001c0001t0001a0001c0001t0005a0001c0001t0013others(111): Show | 286 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(283): Show |
3_prime_UTR_variant | MODIFIER | c.*5548_*5550delAAA | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 5548 | INFO_REALIGN_3_PRIME | chr2 | 112534323 | ||||
chr2:112534323
|
CAAAA | C | 16 | a0001c0001t0092a0001c0002t0008a0001c0002t0009others(13): Show | 27 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*5547_*5550delAAAA | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 5547 | INFO_REALIGN_3_PRIME | chr2 | 112534323 | ||||
chr2:112534412
|
C | G | 1 | a0001c0002t0131 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5617C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 5617 | chr2 | 112534412 | |||||
chr2:112534486
|
G | C | 1 | a0001c0001t0122 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5691G>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 5691 | chr2 | 112534486 | |||||
chr2:112534701
|
A | G | 2 | a0001c0002t0116a0001c0002t0119 | 2 | HG02683.hp1 HG03927.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5906A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 5906 | chr2 | 112534701 | |||||
chr2:112534817
|
C | G | 121 | a0001c0001t0001a0001c0001t0005a0001c0001t0013others(118): Show | 285 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(282): Show |
3_prime_UTR_variant | MODIFIER | c.*6022C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 6022 | chr2 | 112534817 | |||||
chr2:112534872
|
CG | C | 14 | a0001c0002t0006a0001c0002t0009a0001c0002t0012others(11): Show | 31 | HG01243.hp2 HG01257.hp1 HG01258.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*6078delG | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 6078 | chr2 | 112534872 | |||||
chr2:112534893
|
A | G | 1 | a0001c0002t0042 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6098A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 6098 | chr2 | 112534893 | |||||
chr2:112534966
|
G | A | 1 | a0001c0001t0121 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6171G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 6171 | chr2 | 112534966 | |||||
chr2:112535100
|
AAGTT | A | 1 | a0001c0002t0015 | 3 | HG02109.hp2 HG03195.hp1 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6310_*6313delAGTT | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 6310 | INFO_REALIGN_3_PRIME | chr2 | 112535100 | ||||
chr2:112535194
|
G | T | 142 | a0001c0001t0001a0001c0001t0005a0001c0001t0013others(139): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
3_prime_UTR_variant | MODIFIER | c.*6399G>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 6399 | chr2 | 112535194 | |||||
chr2:112535204
|
A | G | 1 | a0001c0003t0011 | 5 | NA18948.hp1 NA18960.hp2 NA18964.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*6409A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 6409 | chr2 | 112535204 | |||||
chr2:112535286
|
A | G | 1 | a0001c0001t0091 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6491A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 6491 | chr2 | 112535286 | |||||
chr2:112535303
|
C | G | 2 | a0001c0001t0126a0001c0002t0131 | 2 | HG02965.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6508C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 6508 | chr2 | 112535303 | |||||
chr2:112535305
|
G | A | 1 | a0001c0001t0124 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6510G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 6510 | chr2 | 112535305 | |||||
chr2:112535365
|
G | A | 5 | a0001c0002t0006a0001c0002t0012a0001c0002t0028others(2): Show | 16 | HG01891.hp1 HG02572.hp2 HG02615.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*6570G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 6570 | chr2 | 112535365 | |||||
chr2:112535396
|
A | G | 3 | a0001c0002t0051a0001c0002t0052a0001c0002t0142 | 3 | HG02896.hp1 HG02922.hp2 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6601A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 6601 | chr2 | 112535396 | |||||
chr2:112535567
|
T | TA | 9 | a0001c0002t0006a0001c0002t0012a0001c0002t0028others(6): Show | 20 | HG01891.hp1 HG02145.hp1 HG02572.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*6773dupA | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 6774 | INFO_REALIGN_3_PRIME | chr2 | 112535567 | ||||
chr2:112535744
|
AT | A | 141 | a0001c0001t0001a0001c0001t0005a0001c0001t0013others(138): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
3_prime_UTR_variant | MODIFIER | c.*6957delT | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 6957 | INFO_REALIGN_3_PRIME | chr2 | 112535744 | ||||
chr2:112535771
|
A | G | 2 | a0001c0002t0051a0001c0002t0052 | 2 | HG02896.hp1 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6976A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 6976 | chr2 | 112535771 | |||||
chr2:112535820
|
T | G | 2 | a0001c0002t0051a0001c0002t0052 | 2 | HG02896.hp1 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7025T>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 7025 | chr2 | 112535820 | |||||
chr2:112535934
|
A | T | 1 | a0001c0001t0090 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7139A>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 7139 | chr2 | 112535934 | |||||
chr2:112535982
|
T | G | 62 | a0001c0001t0014a0001c0001t0026a0001c0001t0032others(59): Show | 151 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(148): Show |
3_prime_UTR_variant | MODIFIER | c.*7187T>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 7187 | chr2 | 112535982 | |||||
chr2:112536004
|
C | T | 2 | a0001c0002t0051a0001c0002t0052 | 2 | HG02896.hp1 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7209C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 7209 | chr2 | 112536004 | |||||
chr2:112536045
|
G | A | 3 | a0001c0002t0008a0001c0002t0043a0001c0002t0044 | 8 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*7250G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 7250 | chr2 | 112536045 | |||||
chr2:112536080
|
G | A | 1 | a0001c0001t0121 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7285G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 7285 | chr2 | 112536080 | |||||
chr2:112536223
|
A | G | 2 | a0001c0001t0048a0001c0001t0050 | 2 | HG01346.hp1 HG02486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7428A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 7428 | chr2 | 112536223 | |||||
chr2:112536239
|
A | T | 1 | a0001c0001t0039 | 2 | HG01981.hp2 NA20752.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7444A>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 7444 | chr2 | 112536239 | |||||
chr2:112536240
|
A | T | 8 | a0001c0001t0025a0001c0001t0039a0001c0001t0088others(5): Show | 11 | HG00738.hp2 HG01256.hp2 HG01258.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*7445A>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 7445 | chr2 | 112536240 | |||||
chr2:112536241
|
T | A | 14 | a0001c0001t0070a0001c0002t0006a0001c0002t0008others(11): Show | 30 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*7446T>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 7446 | chr2 | 112536241 | |||||
chr2:112536311
|
T | G | 1 | a0001c0002t0042 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7516T>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 7516 | chr2 | 112536311 | |||||
chr2:112536354
|
T | C | 1 | a0001c0001t0133 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7559T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 7559 | chr2 | 112536354 | |||||
chr2:112536408
|
A | G | 2 | a0001c0003t0114a0001c0003t0115 | 2 | NA19003.hp2 NA19091.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7613A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 7613 | chr2 | 112536408 | |||||
chr2:112536429
|
A | G | 2 | a0001c0002t0051a0001c0002t0052 | 2 | HG02896.hp1 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7634A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 7634 | chr2 | 112536429 | |||||
chr2:112536721
|
C | T | 76 | a0001c0001t0014a0001c0001t0026a0001c0001t0032others(73): Show | 181 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(178): Show |
3_prime_UTR_variant | MODIFIER | c.*7926C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 7926 | chr2 | 112536721 | |||||
chr2:112536764
|
G | A | 69 | a0001c0001t0014a0001c0001t0026a0001c0001t0032others(66): Show | 169 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(166): Show |
3_prime_UTR_variant | MODIFIER | c.*7969G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 7969 | chr2 | 112536764 | |||||
chr2:112536919
|
A | G | 1 | a0001c0002t0142 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8124A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 8124 | chr2 | 112536919 | |||||
chr2:112537077
|
TTTTG | T | 2 | a0001c0002t0029a0001c0002t0128 | 3 | HG01243.hp2 HG02895.hp2 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8303_*8306delTTTG | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 8303 | INFO_REALIGN_3_PRIME | chr2 | 112537077 | ||||
chr2:112537161
|
A | G | 70 | a0001c0001t0014a0001c0001t0026a0001c0001t0032others(67): Show | 170 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(167): Show |
3_prime_UTR_variant | MODIFIER | c.*8366A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 8366 | chr2 | 112537161 | |||||
chr2:112537166
|
C | T | 1 | a0001c0001t0087 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8371C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 8371 | chr2 | 112537166 | |||||
chr2:112537179
|
T | TA | 70 | a0001c0001t0014a0001c0001t0026a0001c0001t0032others(67): Show | 170 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(167): Show |
3_prime_UTR_variant | MODIFIER | c.*8386dupA | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 8387 | INFO_REALIGN_3_PRIME | chr2 | 112537179 | ||||
chr2:112537363
|
G | T | 3 | a0001c0002t0055a0001c0002t0056a0001c0002t0057 | 3 | HG02145.hp1 HG02647.hp1 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8568G>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 8568 | chr2 | 112537363 | |||||
chr2:112537438
|
A | G | 9 | a0001c0001t0070a0001c0002t0006a0001c0002t0012others(6): Show | 20 | HG01891.hp1 HG02145.hp1 HG02572.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*8643A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 8643 | chr2 | 112537438 | |||||
chr2:112537447
|
C | T | 1 | a0001c0001t0086 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8652C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 8652 | chr2 | 112537447 | |||||
chr2:112537624
|
C | T | 3 | a0001c0001t0023a0001c0001t0024a0001c0001t0122 | 7 | HG01167.hp2 HG01243.hp1 HG02486.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*8829C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 8829 | chr2 | 112537624 | |||||
chr2:112537710
|
C | A | 1 | a0001c0001t0066 | 1 | NA19001.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8915C>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 8915 | chr2 | 112537710 | |||||
chr2:112537904
|
C | G | 1 | a0001c0003t0112 | 1 | HG00735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9109C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 9109 | chr2 | 112537904 | |||||
chr2:112538036
|
G | C | 4 | a0001c0001t0040a0001c0001t0071a0001c0001t0096others(1): Show | 5 | HG01891.hp2 HG02622.hp2 HG02630.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*9241G>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 9241 | chr2 | 112538036 | |||||
chr2:112538046
|
A | G | 10 | a0001c0001t0070a0001c0002t0006a0001c0002t0012others(7): Show | 21 | HG01891.hp1 HG02145.hp1 HG02572.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*9251A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 9251 | chr2 | 112538046 | |||||
chr2:112538275
|
C | T | 2 | a0001c0001t0048a0001c0001t0050 | 2 | HG01346.hp1 HG02486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*9480C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 9480 | chr2 | 112538275 | |||||
chr2:112538358
|
C | T | 1 | a0001c0001t0086 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9563C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 9563 | chr2 | 112538358 | |||||
chr2:112538421
|
A | C | 1 | a0001c0001t0085 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9626A>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 9626 | chr2 | 112538421 | |||||
chr2:112538481
|
G | A | 37 | a0001c0001t0014a0001c0001t0066a0001c0001t0067others(34): Show | 87 | HG00438.hp1 HG00621.hp1 HG00673.hp1 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*9686G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 9686 | chr2 | 112538481 | |||||
chr2:112538526
|
C | T | 1 | a0001c0002t0058 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9731C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 9731 | chr2 | 112538526 | |||||
chr2:112538541
|
G | A | 26 | a0001c0001t0014a0001c0001t0066a0001c0001t0067others(23): Show | 65 | HG00438.hp1 HG00621.hp1 HG00673.hp1 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*9746G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 9746 | chr2 | 112538541 | |||||
chr2:112538626
|
G | C | 36 | a0001c0001t0014a0001c0001t0066a0001c0001t0067others(33): Show | 86 | HG00438.hp1 HG00621.hp1 HG00673.hp1 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*9831G>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 9831 | chr2 | 112538626 | |||||
chr2:112538881
|
G | C | 1 | a0001c0001t0072 | 1 | HG02083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10086G>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 10086 | chr2 | 112538881 | |||||
chr2:112538883
|
C | T | 1 | a0001c0001t0072 | 1 | HG02083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10088C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 10088 | chr2 | 112538883 | |||||
chr2:112538884
|
A | G | 1 | a0001c0001t0072 | 1 | HG02083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10089A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 10089 | chr2 | 112538884 | |||||
chr2:112538888
|
C | T | 1 | a0001c0003t0111 | 1 | HG01981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10093C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 10093 | chr2 | 112538888 | |||||
chr2:112538914
|
A | G | 1 | a0001c0001t0097 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10119A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 10119 | chr2 | 112538914 | |||||
chr2:112538924
|
T | C | 1 | a0001c0001t0073 | 1 | NA18981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10129T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 10129 | chr2 | 112538924 | |||||
chr2:112538931
|
T | C | 1 | a0001c0003t0139 | 1 | NA19090.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10136T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 10136 | chr2 | 112538931 | |||||
chr2:112538955
|
A | C | 1 | a0001c0002t0084 | 1 | HG01168.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10160A>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 10160 | chr2 | 112538955 | |||||
chr2:112538989
|
C | T | 1 | a0001c0001t0083 | 1 | HG00544.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10194C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 10194 | chr2 | 112538989 | |||||
chr2:112539048
|
C | A | 1 | a0001c0001t0074 | 1 | NA18960.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10253C>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 10253 | chr2 | 112539048 | |||||
chr2:112539111
|
T | TA | 13 | a0001c0001t0017a0001c0001t0025a0001c0001t0039others(10): Show | 20 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*10340dupA | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 10341 | INFO_REALIGN_3_PRIME | chr2 | 112539111 | ||||
chr2:112539111
|
T | TAAA | 7 | a0001c0001t0070a0001c0001t0136a0001c0002t0006others(4): Show | 15 | HG01891.hp1 HG02572.hp2 HG02622.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*10338_*10340dupAA others(1): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 10341 | INFO_REALIGN_3_PRIME | chr2 | 112539111 | ||||
chr2:112539111
|
T | TAAAA | 3 | a0001c0002t0012a0001c0002t0053a0001c0002t0054 | 6 | HG02615.hp2 HG02809.hp2 HG02818.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*10337_*10340dupAA others(2): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 10341 | INFO_REALIGN_3_PRIME | chr2 | 112539111 | ||||
chr2:112539111
|
TA | T | 32 | a0001c0001t0014a0001c0001t0065a0001c0001t0066others(29): Show | 74 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*10340delA | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 10340 | INFO_REALIGN_3_PRIME | chr2 | 112539111 | ||||
chr2:112539111
|
TAAAAAAA others(8): Show |
T | 1 | a0001c0002t0036 | 2 | HG00438.hp1 NA18963.hp2 |
3_prime_UTR_variant | MODIFIER | c.*10326_*10340delAA others(13): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 10326 | INFO_REALIGN_3_PRIME | chr2 | 112539111 | ||||
chr2:112539162
|
A | G | 7 | a0001c0001t0065a0001c0002t0008a0001c0002t0043others(4): Show | 12 | HG00099.hp2 HG00140.hp1 HG01358.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*10367A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 10367 | chr2 | 112539162 | |||||
chr2:112539230
|
T | A | 16 | a0001c0001t0066a0001c0001t0067a0001c0001t0068others(13): Show | 51 | HG00438.hp1 HG00621.hp1 HG00673.hp1 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*10435T>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 10435 | chr2 | 112539230 | |||||
chr2:112539265
|
A | G | 7 | a0001c0001t0065a0001c0002t0008a0001c0002t0043others(4): Show | 12 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*10470A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 10470 | chr2 | 112539265 | |||||
chr2:112539293
|
C | T | 42 | a0001c0001t0014a0001c0001t0066a0001c0001t0067others(39): Show | 100 | HG00438.hp1 HG00621.hp1 HG00673.hp1 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*10498C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 10498 | chr2 | 112539293 | |||||
chr2:112539378
|
TTAA | T | 18 | a0001c0001t0025a0001c0001t0039a0001c0001t0040others(15): Show | 22 | HG00738.hp2 HG01256.hp2 HG01258.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*10586_*10588delAT others(1): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 10586 | INFO_REALIGN_3_PRIME | chr2 | 112539378 | ||||
chr2:112539425
|
T | C | 1 | a0001c0001t0063 | 1 | NA18995.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10630T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 10630 | chr2 | 112539425 | |||||
chr2:112539577
|
T | TG | 3 | a0001c0003t0021a0001c0003t0110a0001c0003t0111 | 5 | HG00280.hp1 HG01981.hp1 HG02055.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*10783dupG | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 10784 | INFO_REALIGN_3_PRIME | chr2 | 112539577 | ||||
chr2:112539757
|
C | G | 1 | a0001c0001t0081 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10962C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 10962 | chr2 | 112539757 | |||||
chr2:112539794
|
T | A | 37 | a0001c0001t0014a0001c0001t0066a0001c0001t0067others(34): Show | 89 | HG00438.hp1 HG00621.hp1 HG00673.hp1 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*10999T>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 10999 | chr2 | 112539794 | |||||
chr2:112539994
|
C | T | 1 | a0001c0003t0107 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11199C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 11199 | chr2 | 112539994 | |||||
chr2:112540089
|
T | C | 10 | a0001c0001t0070a0001c0001t0136a0001c0002t0006others(7): Show | 21 | HG01891.hp1 HG02145.hp1 HG02572.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*11294T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 11294 | chr2 | 112540089 | |||||
chr2:112540192
|
CT | C | 1 | a0001c0001t0018 | 3 | HG02040.hp2 NA18998.hp2 NA19066.hp1 |
3_prime_UTR_variant | MODIFIER | c.*11400delT | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 11400 | INFO_REALIGN_3_PRIME | chr2 | 112540192 | ||||
chr2:112540199
|
C | T | 37 | a0001c0001t0014a0001c0001t0066a0001c0001t0067others(34): Show | 89 | HG00438.hp1 HG00621.hp1 HG00673.hp1 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*11404C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 11404 | chr2 | 112540199 | |||||
chr2:112540208
|
C | G | 2 | a0001c0001t0136a0001c0002t0056 | 2 | HG02717.hp1 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*11413C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 11413 | chr2 | 112540208 | |||||
chr2:112540273
|
A | C | 1 | a0001c0001t0080 | 1 | NA19005.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11478A>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 11478 | chr2 | 112540273 | |||||
chr2:112540419
|
A | G | 6 | a0001c0001t0070a0001c0002t0006a0001c0002t0012others(3): Show | 17 | HG01891.hp1 HG02572.hp2 HG02615.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*11624A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 11624 | chr2 | 112540419 | |||||
chr2:112540433
|
C | CA | 15 | a0001c0001t0070a0001c0001t0076a0001c0001t0085others(12): Show | 26 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*11654dupA | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 11655 | INFO_REALIGN_3_PRIME | chr2 | 112540433 | ||||
chr2:112540433
|
CA | C | 64 | a0001c0001t0005a0001c0001t0014a0001c0001t0059others(61): Show | 151 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(148): Show |
3_prime_UTR_variant | MODIFIER | c.*11654delA | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 11654 | INFO_REALIGN_3_PRIME | chr2 | 112540433 | ||||
chr2:112540441
|
A | C | 31 | a0001c0001t0014a0001c0001t0065a0001c0001t0066others(28): Show | 77 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*11646A>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 11646 | chr2 | 112540441 | |||||
chr2:112540445
|
A | G | 22 | a0001c0001t0001a0001c0001t0013a0001c0001t0016others(19): Show | 78 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*11650A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 11650 | chr2 | 112540445 | |||||
chr2:112540447
|
AAAG | A | 25 | a0001c0001t0001a0001c0001t0013a0001c0001t0016others(22): Show | 81 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*11654_*11656delAG others(1): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 11654 | INFO_REALIGN_3_PRIME | chr2 | 112540447 | ||||
chr2:112540448
|
A | G | 3 | a0001c0001t0031a0001c0001t0072a0001c0002t0140 | 4 | HG00438.hp2 HG02083.hp2 HG02165.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*11653A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 11653 | chr2 | 112540448 | |||||
chr2:112540450
|
G | A | 3 | a0001c0001t0031a0001c0001t0072a0001c0002t0140 | 4 | HG00438.hp2 HG02083.hp2 HG02165.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*11655G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 11655 | chr2 | 112540450 | |||||
chr2:112540608
|
A | G | 1 | a0001c0001t0078 | 1 | NA18992.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11813A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 11813 | chr2 | 112540608 | |||||
chr2:112540743
|
CTT | C | 3 | a0001c0002t0015a0001c0002t0029a0001c0002t0128 | 6 | HG01243.hp2 HG02109.hp2 HG02895.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*11952_*11953delTT | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 11952 | INFO_REALIGN_3_PRIME | chr2 | 112540743 | ||||
chr2:112540783
|
G | T | 1 | a0001c0001t0079 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11988G>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 11988 | chr2 | 112540783 | |||||
chr2:112540910
|
T | C | 1 | a0001c0001t0075 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*12115T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 12115 | chr2 | 112540910 | |||||
chr2:112541009
|
T | C | 58 | a0001c0001t0001a0001c0001t0013a0001c0001t0016others(55): Show | 132 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(129): Show |
3_prime_UTR_variant | MODIFIER | c.*12214T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 12214 | chr2 | 112541009 | |||||
chr2:112541053
|
A | G | 5 | a0001c0002t0009a0001c0002t0015a0001c0002t0029others(2): Show | 13 | HG01243.hp2 HG01257.hp1 HG01258.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*12258A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 12258 | chr2 | 112541053 | |||||
chr2:112541106
|
A | G | 1 | a0001c0002t0042 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*12311A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 12311 | chr2 | 112541106 | |||||
chr2:112541214
|
G | A | 3 | a0001c0002t0020a0001c0003t0020a0001c0003t0138 | 4 | HG02886.hp2 HG03453.hp1 HG03540.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*12419G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 12419 | chr2 | 112541214 | |||||
chr2:112541239
|
A | G | 5 | a0001c0002t0009a0001c0002t0015a0001c0002t0029others(2): Show | 13 | HG01243.hp2 HG01257.hp1 HG01258.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*12444A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 12444 | chr2 | 112541239 | |||||
chr2:112541251
|
C | G | 52 | a0001c0001t0001a0001c0001t0013a0001c0001t0016others(49): Show | 118 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(115): Show |
3_prime_UTR_variant | MODIFIER | c.*12456C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 12456 | chr2 | 112541251 | |||||
chr2:112541326
|
C | A | 1 | a0001c0002t0042 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*12531C>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 12531 | chr2 | 112541326 | |||||
chr2:112541330
|
T | C | 1 | a0001c0003t0027 | 3 | NA18971.hp2 NA18980.hp1 NA18985.hp1 |
3_prime_UTR_variant | MODIFIER | c.*12535T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 12535 | chr2 | 112541330 | |||||
chr2:112541431
|
T | C | 3 | a0001c0001t0048a0001c0001t0050a0001c0002t0042 | 3 | HG01346.hp1 HG02486.hp1 HG03927.hp2 |
3_prime_UTR_variant | MODIFIER | c.*12636T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 12636 | chr2 | 112541431 | |||||
chr2:112541560
|
CAG | C | 2 | a0001c0001t0014a0001c0001t0100 | 5 | HG01109.hp1 HG02055.hp1 HG02257.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*12766_*12767delAG | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 12766 | chr2 | 112541560 | |||||
chr2:112541592
|
T | C | 1 | a0001c0001t0094 | 1 | HG01952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*12797T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 7/7 | 12797 | chr2 | 112541592 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:112482520
|
C | T | 1 | a0001c0001t0132g0305 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.157+19C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 1/6 | chr2 | 112482520 | ||||||
chr2:112482551
|
G | T | 1 | a0001c0001t0001g0304 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.157+50G>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 1/6 | chr2 | 112482551 | ||||||
chr2:112482606
|
T | C | 72 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0087others(69): Show | 74 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(71): Show |
intron_variant | MODIFIER | c.157+105T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 1/6 | chr2 | 112482606 | ||||||
chr2:112482702
|
C | T | 1 | a0001c0003t0003g0303 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.157+201C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 1/6 | chr2 | 112482702 | ||||||
chr2:112482762
|
A | G | 1 | a0001c0002t0008g0089 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.157+261A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 1/6 | chr2 | 112482762 | ||||||
chr2:112482773
|
C | G | 2 | a0001c0002t0036g0301a0001c0002t0036g0302 | 2 | HG00438.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.157+272C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 1/6 | chr2 | 112482773 | ||||||
chr2:112482794
|
C | T | 1 | a0001c0003t0011g0023 | 2 | NA18960.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.157+293C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 1/6 | chr2 | 112482794 | ||||||
chr2:112482820
|
C | A | 2 | a0001c0001t0076g0090a0001c0001t0096g0091 | 2 | HG02922.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.157+319C>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 1/6 | chr2 | 112482820 | ||||||
chr2:112482847
|
G | GTCCGCCG others(13): Show |
1 | a0001c0001t0001g0087 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.157+352_157+371dup others(20): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 112482847 | |||||
chr2:112482853
|
C | G | 1 | a0001c0002t0042g0088 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.157+352C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 1/6 | chr2 | 112482853 | ||||||
chr2:112482862
|
C | CGCTGG | 4 | a0001c0003t0003g0299a0001c0003t0011g0023a0001c0003t0011g0298others(1): Show | 5 | NA18948.hp2 NA18960.hp2 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.157+363_157+364ins others(5): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 112482862 | |||||
chr2:112482867
|
C | G | 4 | a0001c0003t0003g0299a0001c0003t0011g0023a0001c0003t0011g0298others(1): Show | 5 | NA18948.hp2 NA18960.hp2 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.157+366C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 1/6 | chr2 | 112482867 | ||||||
chr2:112482985
|
C | T | 4 | a0001c0002t0009g0294a0001c0002t0009g0295a0001c0002t0009g0296others(1): Show | 4 | HG01257.hp1 HG01258.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.157+484C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 1/6 | chr2 | 112482985 | ||||||
chr2:112482990
|
C | A | 1 | a0001c0001t0132g0305 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.157+489C>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 1/6 | chr2 | 112482990 | ||||||
chr2:112482990
|
C | T | 1 | a0001c0001t0090g0293 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.157+489C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 1/6 | chr2 | 112482990 | ||||||
chr2:112483127
|
T | A | 1 | a0001c0001t0135g0024 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.157+626T>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 1/6 | chr2 | 112483127 | ||||||
chr2:112483340
|
G | C | 53 | a0001c0001t0007g0037a0001c0001t0007g0038a0001c0001t0007g0051others(50): Show | 55 | HG00639.hp1 HG00738.hp2 HG01074.hp2 others(52): Show |
intron_variant | MODIFIER | c.157+839G>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 1/6 | chr2 | 112483340 | ||||||
chr2:112483344
|
G | T | 29 | a0001c0001t0007g0051a0001c0001t0007g0052a0001c0001t0007g0053others(26): Show | 30 | HG00639.hp1 HG01074.hp2 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.157+843G>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 1/6 | chr2 | 112483344 | ||||||
chr2:112483385
|
C | T | 1 | a0001c0002t0042g0088 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.157+884C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 1/6 | chr2 | 112483385 | ||||||
chr2:112484210
|
C | T | 1 | a0001c0001t0077g0292 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.158-1707C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 1/6 | chr2 | 112484210 | ||||||
chr2:112484234
|
G | GT | 13 | a0001c0001t0005g0287a0001c0001t0014g0044a0001c0001t0018g0288others(10): Show | 13 | HG00741.hp2 HG01109.hp1 HG01952.hp1 others(10): Show |
intron_variant | MODIFIER | c.158-1668dupT | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 112484234 | |||||
chr2:112484234
|
GT | G | 12 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0087others(9): Show | 12 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(9): Show |
intron_variant | MODIFIER | c.158-1668delT | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 112484234 | |||||
chr2:112484302
|
C | T | 4 | a0001c0001t0088g0086a0001c0002t0015g0083a0001c0002t0015g0084others(1): Show | 4 | HG02109.hp2 HG03195.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.158-1615C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 1/6 | chr2 | 112484302 | ||||||
chr2:112484354
|
C | T | 1 | a0001c0001t0133g0043 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.158-1563C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 1/6 | chr2 | 112484354 | ||||||
chr2:112484408
|
C | T | 4 | a0001c0001t0088g0086a0001c0002t0015g0083a0001c0002t0015g0084others(1): Show | 4 | HG02109.hp2 HG03195.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.158-1509C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 1/6 | chr2 | 112484408 | ||||||
chr2:112484466
|
T | G | 1 | a0001c0002t0020g0093 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.158-1451T>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 1/6 | chr2 | 112484466 | ||||||
chr2:112484645
|
C | G | 3 | a0001c0002t0020g0093a0001c0002t0055g0279a0001c0002t0057g0280 | 3 | HG02145.hp1 HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.158-1272C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 1/6 | chr2 | 112484645 | ||||||
chr2:112484688
|
A | G | 2 | a0001c0001t0025g0009a0001c0001t0025g0042 | 3 | HG00738.hp2 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.158-1229A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 1/6 | chr2 | 112484688 | ||||||
chr2:112484781
|
C | G | 1 | a0001c0002t0020g0093 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.158-1136C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 1/6 | chr2 | 112484781 | ||||||
chr2:112484988
|
C | T | 1 | a0001c0001t0001g0278 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.158-929C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 1/6 | chr2 | 112484988 | ||||||
chr2:112485050
|
A | G | 3 | a0001c0002t0020g0093a0001c0002t0055g0279a0001c0002t0057g0280 | 3 | HG02145.hp1 HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.158-867A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 1/6 | chr2 | 112485050 | ||||||
chr2:112485711
|
A | G | 2 | a0001c0001t0070g0082a0001c0002t0045g0081 | 2 | HG03209.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.158-206A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 1/6 | chr2 | 112485711 | ||||||
chr2:112485744
|
G | A | 228 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(225): Show | 249 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.158-173G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 1/6 | chr2 | 112485744 | ||||||
chr2:112485877
|
G | GGGGCTGA others(17): Show |
31 | a0001c0001t0023g0011a0001c0001t0023g0101a0001c0001t0024g0007others(28): Show | 35 | HG01167.hp2 HG01243.hp1 HG01257.hp1 others(32): Show |
intron_variant | MODIFIER | c.158-40_158-39insGG others(22): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 1/6 | chr2 | 112485877 | ||||||
chr2:112486113
|
A | G | 1 | a0001c0003t0003g0239 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.236+118A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112486113 | ||||||
chr2:112486137
|
G | A | 1 | a0001c0001t0093g0240 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.236+142G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112486137 | ||||||
chr2:112486197
|
A | G | 2 | a0001c0001t0088g0086a0001c0001t0130g0041 | 2 | HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.236+202A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112486197 | ||||||
chr2:112486222
|
T | A | 12 | a0001c0001t0001g0077a0001c0001t0001g0087a0001c0001t0070g0082others(9): Show | 12 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(9): Show |
intron_variant | MODIFIER | c.236+227T>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112486222 | ||||||
chr2:112486345
|
C | G | 2 | a0001c0002t0116g0289a0001c0002t0119g0238 | 2 | HG02683.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.236+350C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112486345 | ||||||
chr2:112486355
|
C | G | 2 | a0001c0002t0051g0237a0001c0002t0052g0236 | 2 | HG02896.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.236+360C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112486355 | ||||||
chr2:112486438
|
T | C | 1 | a0001c0001t0026g0056 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.236+443T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112486438 | ||||||
chr2:112486447
|
A | T | 2 | a0001c0002t0051g0237a0001c0002t0052g0236 | 2 | HG02896.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.236+452A>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112486447 | ||||||
chr2:112486675
|
G | C | 290 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0016others(287): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.236+680G>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112486675 | ||||||
chr2:112486682
|
G | C | 2 | a0001c0001t0076g0090a0001c0001t0090g0293 | 2 | HG02922.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.236+687G>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112486682 | ||||||
chr2:112486721
|
C | T | 13 | a0001c0001t0013g0063a0001c0003t0003g0226a0001c0003t0003g0227others(10): Show | 13 | HG02129.hp1 NA18945.hp2 NA18948.hp1 others(10): Show |
intron_variant | MODIFIER | c.236+726C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112486721 | ||||||
chr2:112486759
|
G | A | 1 | a0001c0003t0004g0113 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.236+764G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112486759 | ||||||
chr2:112486946
|
C | T | 1 | a0001c0002t0057g0280 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.236+951C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112486946 | ||||||
chr2:112487064
|
G | A | 1 | a0001c0001t0086g0114 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.236+1069G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112487064 | ||||||
chr2:112487092
|
C | T | 130 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0016others(127): Show | 143 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.236+1097C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112487092 | ||||||
chr2:112487093
|
A | G | 130 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0016others(127): Show | 143 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.236+1098A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112487093 | ||||||
chr2:112487170
|
C | T | 1 | a0001c0003t0137g0026 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.236+1175C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112487170 | ||||||
chr2:112487383
|
A | G | 13 | a0001c0001t0001g0087a0001c0002t0008g0070a0001c0002t0008g0072others(10): Show | 13 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(10): Show |
intron_variant | MODIFIER | c.236+1388A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112487383 | ||||||
chr2:112487556
|
G | A | 1 | a0001c0001t0070g0082 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.236+1561G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112487556 | ||||||
chr2:112487866
|
T | C | 292 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0016others(289): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.236+1871T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112487866 | ||||||
chr2:112487870
|
T | G | 1 | a0001c0001t0007g0051 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.236+1875T>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112487870 | ||||||
chr2:112488084
|
A | G | 307 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0016others(304): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.236+2089A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112488084 | ||||||
chr2:112488150
|
C | T | 2 | a0001c0002t0002g0185a0001c0002t0002g0186 | 2 | NA18981.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.236+2155C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112488150 | ||||||
chr2:112488434
|
G | A | 12 | a0001c0002t0008g0070a0001c0002t0008g0072a0001c0002t0008g0074others(9): Show | 12 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(9): Show |
intron_variant | MODIFIER | c.236+2439G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112488434 | ||||||
chr2:112488483
|
C | T | 1 | a0001c0002t0057g0280 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.236+2488C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112488483 | ||||||
chr2:112488588
|
T | C | 1 | a0001c0003t0020g0115 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.236+2593T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112488588 | ||||||
chr2:112488766
|
AG | A | 8 | a0001c0001t0076g0090a0001c0001t0098g0277a0001c0002t0002g0181others(5): Show | 8 | HG01070.hp2 HG02040.hp1 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.236+2772delG | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112488766 | ||||||
chr2:112488767
|
G | A | 284 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0016others(281): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.236+2772G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112488767 | ||||||
chr2:112488859
|
C | T | 73 | a0001c0003t0002g0170a0001c0003t0002g0172a0001c0003t0003g0004others(70): Show | 81 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.236+2864C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112488859 | ||||||
chr2:112488960
|
G | A | 1 | a0001c0001t0030g0244 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.236+2965G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112488960 | ||||||
chr2:112489032
|
A | C | 1 | a0001c0002t0002g0080 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.236+3037A>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112489032 | ||||||
chr2:112489085
|
T | C | 1 | a0001c0001t0001g0245 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.236+3090T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112489085 | ||||||
chr2:112489197
|
C | T | 1 | a0001c0001t0095g0225 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.236+3202C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112489197 | ||||||
chr2:112489273
|
C | T | 1 | a0001c0001t0050g0276 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.236+3278C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112489273 | ||||||
chr2:112489283
|
C | G | 2 | a0001c0001t0048g0275a0001c0001t0050g0276 | 2 | HG01346.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.236+3288C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112489283 | ||||||
chr2:112489370
|
A | C | 12 | a0001c0002t0008g0070a0001c0002t0008g0072a0001c0002t0008g0074others(9): Show | 12 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(9): Show |
intron_variant | MODIFIER | c.236+3375A>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112489370 | ||||||
chr2:112489396
|
C | T | 1 | a0001c0002t0042g0088 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.236+3401C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112489396 | ||||||
chr2:112489444
|
G | T | 1 | a0001c0001t0018g0224 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.236+3449G>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112489444 | ||||||
chr2:112489462
|
A | C | 3 | a0001c0003t0003g0242a0001c0003t0034g0180a0001c0003t0035g0243 | 3 | HG02083.hp1 HG04184.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.236+3467A>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112489462 | ||||||
chr2:112489726
|
G | C | 16 | a0001c0002t0006g0012a0001c0002t0006g0104a0001c0002t0006g0106others(13): Show | 17 | HG02572.hp2 HG02615.hp2 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.236+3731G>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112489726 | ||||||
chr2:112489912
|
A | T | 1 | a0001c0001t0040g0050 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.236+3917A>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112489912 | ||||||
chr2:112490039
|
G | T | 4 | a0001c0002t0020g0093a0001c0002t0028g0097a0001c0002t0028g0146others(1): Show | 4 | HG01891.hp1 HG02647.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.236+4044G>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112490039 | ||||||
chr2:112490043
|
C | G | 71 | a0001c0003t0002g0170a0001c0003t0002g0172a0001c0003t0003g0004others(68): Show | 79 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.236+4048C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112490043 | ||||||
chr2:112490059
|
C | T | 12 | a0001c0001t0014g0030a0001c0001t0014g0031a0001c0001t0014g0033others(9): Show | 12 | HG01109.hp1 HG01346.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.236+4064C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112490059 | ||||||
chr2:112490178
|
G | A | 75 | a0001c0002t0051g0237a0001c0002t0052g0236a0001c0003t0002g0170others(72): Show | 83 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.237-3965G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112490178 | ||||||
chr2:112490213
|
C | T | 12 | a0001c0001t0014g0030a0001c0001t0014g0031a0001c0001t0014g0033others(9): Show | 12 | HG01109.hp1 HG01346.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.237-3930C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112490213 | ||||||
chr2:112490291
|
G | A | 1 | a0001c0002t0056g0094 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.237-3852G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112490291 | ||||||
chr2:112490410
|
C | A | 1 | a0001c0001t0098g0277 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.237-3733C>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112490410 | ||||||
chr2:112490559
|
T | A | 2 | a0001c0002t0127g0039a0001c0002t0129g0069 | 2 | HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.237-3584T>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112490559 | ||||||
chr2:112490568
|
C | CT | 15 | a0001c0001t0001g0022a0001c0001t0001g0078a0001c0001t0001g0092others(12): Show | 16 | HG00099.hp1 HG01070.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.237-3553dupT | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 112490568 | |||||
chr2:112490568
|
CT | C | 31 | a0001c0001t0001g0191a0001c0001t0087g0190a0001c0002t0002g0140others(28): Show | 32 | HG01257.hp1 HG01891.hp1 HG02135.hp1 others(29): Show |
intron_variant | MODIFIER | c.237-3553delT | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 112490568 | |||||
chr2:112490568
|
CTT | C | 67 | a0001c0002t0002g0003a0001c0002t0002g0008a0001c0002t0002g0013others(64): Show | 71 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.237-3554_237-3553d others(4): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 112490568 | |||||
chr2:112490568
|
CTTTTTT | C | 66 | a0001c0003t0002g0170a0001c0003t0002g0172a0001c0003t0003g0004others(63): Show | 74 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.237-3558_237-3553d others(8): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 112490568 | |||||
chr2:112490571
|
T | C | 2 | a0001c0002t0051g0237a0001c0002t0052g0236 | 2 | HG02896.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.237-3572T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112490571 | ||||||
chr2:112490655
|
C | T | 18 | a0001c0001t0001g0001a0001c0001t0005g0001a0001c0001t0005g0215others(15): Show | 21 | HG01361.hp2 HG01496.hp2 HG01952.hp2 others(18): Show |
intron_variant | MODIFIER | c.237-3488C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112490655 | ||||||
chr2:112490675
|
G | A | 1 | a0001c0003t0003g0303 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.237-3468G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112490675 | ||||||
chr2:112490727
|
A | G | 12 | a0001c0002t0008g0070a0001c0002t0008g0072a0001c0002t0008g0074others(9): Show | 12 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(9): Show |
intron_variant | MODIFIER | c.237-3416A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112490727 | ||||||
chr2:112490784
|
G | A | 3 | a0001c0002t0029g0187a0001c0002t0029g0188a0001c0002t0128g0040 | 3 | HG01243.hp2 HG02895.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.237-3359G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112490784 | ||||||
chr2:112490938
|
C | G | 12 | a0001c0001t0014g0030a0001c0001t0014g0031a0001c0001t0014g0033others(9): Show | 12 | HG01109.hp1 HG01346.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.237-3205C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112490938 | ||||||
chr2:112490999
|
C | T | 1 | a0001c0001t0005g0221 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.237-3144C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112490999 | ||||||
chr2:112491055
|
G | A | 1 | a0001c0001t0001g0246 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.237-3088G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112491055 | ||||||
chr2:112491096
|
A | G | 12 | a0001c0002t0008g0070a0001c0002t0008g0072a0001c0002t0008g0074others(9): Show | 12 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(9): Show |
intron_variant | MODIFIER | c.237-3047A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112491096 | ||||||
chr2:112491125
|
G | A | 2 | a0001c0003t0105g0147a0001c0003t0137g0026 | 2 | HG01074.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.237-3018G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112491125 | ||||||
chr2:112491390
|
T | C | 75 | a0001c0002t0051g0237a0001c0002t0052g0236a0001c0003t0002g0170others(72): Show | 83 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.237-2753T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112491390 | ||||||
chr2:112491545
|
T | C | 3 | a0001c0002t0015g0083a0001c0002t0015g0084a0001c0002t0015g0085 | 3 | HG02109.hp2 HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.237-2598T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112491545 | ||||||
chr2:112491743
|
A | G | 3 | a0001c0002t0020g0093a0001c0002t0028g0097a0001c0002t0028g0146 | 3 | HG01891.hp1 HG03453.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.237-2400A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112491743 | ||||||
chr2:112491768
|
A | G | 3 | a0001c0002t0029g0187a0001c0002t0029g0188a0001c0002t0128g0040 | 3 | HG01243.hp2 HG02895.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.237-2375A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112491768 | ||||||
chr2:112492056
|
C | T | 1 | a0001c0002t0116g0289 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.237-2087C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112492056 | ||||||
chr2:112492259
|
T | C | 1 | a0001c0002t0055g0279 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.237-1884T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112492259 | ||||||
chr2:112492274
|
G | A | 1 | a0001c0001t0085g0145 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.237-1869G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112492274 | ||||||
chr2:112492354
|
G | A | 2 | a0001c0002t0009g0297a0001c0002t0058g0096 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.237-1789G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112492354 | ||||||
chr2:112492444
|
G | A | 1 | a0001c0001t0001g0222 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.237-1699G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112492444 | ||||||
chr2:112492742
|
T | A | 16 | a0001c0002t0006g0012a0001c0002t0006g0104a0001c0002t0006g0106others(13): Show | 17 | HG02572.hp2 HG02615.hp2 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.237-1401T>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112492742 | ||||||
chr2:112492783
|
C | T | 73 | a0001c0003t0002g0170a0001c0003t0002g0172a0001c0003t0003g0004others(70): Show | 81 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.237-1360C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112492783 | ||||||
chr2:112492904
|
A | T | 1 | a0001c0001t0062g0213 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.237-1239A>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112492904 | ||||||
chr2:112492952
|
T | C | 54 | a0001c0002t0002g0003a0001c0002t0002g0008a0001c0002t0002g0013others(51): Show | 58 | HG00438.hp1 HG00621.hp1 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.237-1191T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112492952 | ||||||
chr2:112493135
|
T | G | 51 | a0001c0002t0002g0003a0001c0002t0002g0008a0001c0002t0002g0013others(48): Show | 55 | HG00438.hp1 HG00621.hp1 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.237-1008T>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112493135 | ||||||
chr2:112493160
|
G | A | 54 | a0001c0002t0002g0003a0001c0002t0002g0008a0001c0002t0002g0013others(51): Show | 58 | HG00438.hp1 HG00621.hp1 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.237-983G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112493160 | ||||||
chr2:112493212
|
G | A | 1 | a0001c0002t0028g0146 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.237-931G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112493212 | ||||||
chr2:112493215
|
C | G | 1 | a0001c0002t0051g0237 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.237-928C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112493215 | ||||||
chr2:112493355
|
T | TA | 80 | a0001c0002t0020g0093a0001c0002t0028g0097a0001c0002t0028g0146others(77): Show | 88 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.237-774dupA | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 112493355 | |||||
chr2:112493423
|
C | T | 184 | a0001c0001t0014g0030a0001c0001t0014g0031a0001c0001t0014g0033others(181): Show | 197 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.237-720C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112493423 | ||||||
chr2:112493570
|
A | T | 1 | a0001c0001t0086g0114 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.237-573A>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112493570 | ||||||
chr2:112493571
|
T | C | 1 | a0001c0002t0042g0088 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.237-572T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112493571 | ||||||
chr2:112493582
|
G | A | 16 | a0001c0002t0006g0012a0001c0002t0006g0104a0001c0002t0006g0106others(13): Show | 17 | HG02572.hp2 HG02615.hp2 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.237-561G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112493582 | ||||||
chr2:112493764
|
C | G | 1 | a0001c0001t0088g0086 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.237-379C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112493764 | ||||||
chr2:112493826
|
A | G | 7 | a0001c0002t0009g0143a0001c0002t0009g0144a0001c0002t0009g0294others(4): Show | 7 | HG01257.hp1 HG01258.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.237-317A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112493826 | ||||||
chr2:112493966
|
C | T | 1 | a0001c0002t0057g0280 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.237-177C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112493966 | ||||||
chr2:112494134
|
A | T | 4 | a0001c0001t0014g0031a0001c0001t0014g0033a0001c0001t0014g0044others(1): Show | 4 | HG01109.hp1 HG02055.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.237-9A>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 2/6 | chr2 | 112494134 | ||||||
chr2:112494445
|
C | T | 1 | a0001c0001t0077g0292 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.469+70C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112494445 | ||||||
chr2:112494467
|
G | A | 1 | a0001c0002t0002g0116 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.469+92G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112494467 | ||||||
chr2:112494540
|
T | C | 7 | a0001c0002t0009g0143a0001c0002t0009g0144a0001c0002t0009g0294others(4): Show | 7 | HG01257.hp1 HG01258.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.469+165T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112494540 | ||||||
chr2:112494685
|
T | C | 1 | a0001c0002t0128g0040 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.469+310T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112494685 | ||||||
chr2:112494713
|
CT | C | 3 | a0001c0001t0076g0090a0001c0001t0085g0145a0001c0001t0090g0293 | 3 | HG02922.hp1 NA19240.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.469+339delT | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112494713 | ||||||
chr2:112494762
|
C | G | 1 | a0001c0003t0004g0113 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.469+387C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112494762 | ||||||
chr2:112494826
|
A | G | 75 | a0001c0002t0051g0237a0001c0002t0052g0236a0001c0003t0002g0170others(72): Show | 83 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.469+451A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112494826 | ||||||
chr2:112494849
|
C | T | 1 | a0001c0002t0009g0144 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.469+474C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112494849 | ||||||
chr2:112494888
|
T | C | 7 | a0001c0002t0009g0143a0001c0002t0009g0144a0001c0002t0009g0294others(4): Show | 7 | HG01257.hp1 HG01258.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.469+513T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112494888 | ||||||
chr2:112495011
|
G | A | 7 | a0001c0002t0009g0143a0001c0002t0009g0144a0001c0002t0009g0294others(4): Show | 7 | HG01257.hp1 HG01258.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.469+636G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112495011 | ||||||
chr2:112495148
|
A | G | 16 | a0001c0002t0006g0012a0001c0002t0006g0104a0001c0002t0006g0106others(13): Show | 17 | HG02572.hp2 HG02615.hp2 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.469+773A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112495148 | ||||||
chr2:112495188
|
T | C | 1 | a0001c0003t0004g0148 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.469+813T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112495188 | ||||||
chr2:112495250
|
C | T | 1 | a0001c0001t0134g0029 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.469+875C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112495250 | ||||||
chr2:112495421
|
A | G | 12 | a0001c0002t0008g0070a0001c0002t0008g0072a0001c0002t0008g0074others(9): Show | 12 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(9): Show |
intron_variant | MODIFIER | c.469+1046A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112495421 | ||||||
chr2:112495482
|
T | C | 1 | a0001c0001t0088g0086 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.469+1107T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112495482 | ||||||
chr2:112495601
|
G | A | 172 | a0001c0002t0002g0003a0001c0002t0002g0008a0001c0002t0002g0013others(169): Show | 185 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.469+1226G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112495601 | ||||||
chr2:112495613
|
C | T | 16 | a0001c0002t0006g0012a0001c0002t0006g0104a0001c0002t0006g0106others(13): Show | 17 | HG02572.hp2 HG02615.hp2 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.469+1238C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112495613 | ||||||
chr2:112495657
|
C | T | 5 | a0001c0001t0007g0051a0001c0001t0007g0052a0001c0001t0007g0053others(2): Show | 5 | HG00639.hp1 HG02717.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.469+1282C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112495657 | ||||||
chr2:112495675
|
G | A | 159 | a0001c0002t0002g0003a0001c0002t0002g0008a0001c0002t0002g0013others(156): Show | 172 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.469+1300G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112495675 | ||||||
chr2:112495728
|
T | C | 2 | a0001c0001t0032g0192a0001c0001t0032g0193 | 2 | HG01175.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.469+1353T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112495728 | ||||||
chr2:112495764
|
G | A | 73 | a0001c0003t0002g0170a0001c0003t0002g0172a0001c0003t0003g0004others(70): Show | 81 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.469+1389G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112495764 | ||||||
chr2:112495846
|
T | TA | 75 | a0001c0002t0051g0237a0001c0002t0052g0236a0001c0003t0002g0170others(72): Show | 83 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.469+1481dupA | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 112495846 | |||||
chr2:112495962
|
G | C | 2 | a0001c0001t0048g0275a0001c0001t0050g0276 | 2 | HG01346.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.469+1587G>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112495962 | ||||||
chr2:112495974
|
A | G | 1 | a0001c0002t0131g0034 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.469+1599A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112495974 | ||||||
chr2:112496108
|
C | T | 12 | a0001c0002t0008g0070a0001c0002t0008g0072a0001c0002t0008g0074others(9): Show | 12 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(9): Show |
intron_variant | MODIFIER | c.469+1733C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112496108 | ||||||
chr2:112496194
|
C | A | 5 | a0001c0002t0020g0093a0001c0002t0028g0097a0001c0002t0028g0146others(2): Show | 5 | HG01891.hp1 HG02145.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.469+1819C>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112496194 | ||||||
chr2:112496569
|
A | G | 172 | a0001c0002t0002g0003a0001c0002t0002g0008a0001c0002t0002g0013others(169): Show | 185 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.469+2194A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112496569 | ||||||
chr2:112496665
|
C | CTG | 72 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0016others(69): Show | 82 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.469+2332_469+2333d others(4): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 112496665 | |||||
chr2:112496665
|
C | CTGTG | 20 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0208others(17): Show | 22 | HG00438.hp2 HG00673.hp2 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.469+2330_469+2333d others(6): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 112496665 | |||||
chr2:112496665
|
C | CTGTGTG | 10 | a0001c0001t0013g0063a0001c0001t0014g0031a0001c0001t0014g0033others(7): Show | 10 | HG01109.hp1 HG01496.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.469+2328_469+2333d others(8): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 112496665 | |||||
chr2:112496665
|
CTG | C | 59 | a0001c0001t0001g0077a0001c0001t0001g0246a0001c0001t0001g0271others(56): Show | 67 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.469+2332_469+2333d others(4): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 112496665 | |||||
chr2:112496665
|
CTGTG | C | 16 | a0001c0001t0031g0290a0001c0002t0006g0104a0001c0002t0008g0070others(13): Show | 16 | HG00140.hp1 HG00280.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.469+2330_469+2333d others(6): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 112496665 | |||||
chr2:112496665
|
CTGTGTG | C | 4 | a0001c0002t0142g0095a0001c0003t0003g0226a0001c0003t0105g0147others(1): Show | 4 | HG01074.hp1 HG02280.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.469+2328_469+2333d others(8): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 112496665 | |||||
chr2:112496665
|
CTGTGTGT others(1): Show |
C | 5 | a0001c0002t0053g0233a0001c0002t0054g0234a0001c0002t0127g0039others(2): Show | 5 | HG00735.hp1 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.469+2326_469+2333d others(10): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 112496665 | |||||
chr2:112496665
|
CTGTGTGT others(3): Show |
C | 5 | a0001c0002t0009g0143a0001c0002t0009g0144a0001c0002t0009g0296others(2): Show | 5 | HG01884.hp2 HG02280.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.469+2324_469+2333d others(12): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 112496665 | |||||
chr2:112496665
|
CTGTGTGT others(5): Show |
C | 3 | a0001c0002t0009g0294a0001c0002t0009g0295a0001c0002t0131g0034 | 3 | HG01257.hp1 HG01258.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.469+2322_469+2333d others(14): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 112496665 | |||||
chr2:112496665
|
CTGTGTGT others(7): Show |
C | 6 | a0001c0001t0001g0247a0001c0001t0001g0278a0001c0001t0016g0194others(3): Show | 6 | HG01256.hp1 HG01346.hp1 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.469+2320_469+2333d others(16): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 112496665 | |||||
chr2:112496665
|
CTGTGTGT others(11): Show |
C | 1 | a0001c0001t0040g0050 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.469+2316_469+2333d others(20): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 112496665 | |||||
chr2:112496697
|
G | A | 1 | a0001c0001t0017g0250 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.469+2322G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112496697 | ||||||
chr2:112496698
|
TGTGTGTG others(4): Show |
T | 2 | a0001c0001t0017g0250a0001c0002t0019g0117 | 2 | HG02738.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.469+2324_469+2334d others(13): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112496698 | ||||||
chr2:112496700
|
TGTGTGTG others(2): Show |
T | 14 | a0001c0002t0002g0003a0001c0002t0002g0116a0001c0002t0002g0118others(11): Show | 15 | HG00735.hp2 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.469+2326_469+2334d others(11): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112496700 | ||||||
chr2:112496702
|
TGTGTGTA | T | 38 | a0001c0002t0002g0008a0001c0002t0002g0013a0001c0002t0002g0014others(35): Show | 41 | HG00438.hp1 HG00621.hp1 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.469+2328_469+2334d others(9): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112496702 | ||||||
chr2:112496703
|
G | A | 1 | a0001c0001t0133g0043 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.469+2328G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112496703 | ||||||
chr2:112496706
|
TGTA | T | 4 | a0001c0001t0040g0046a0001c0003t0010g0064a0001c0003t0021g0152others(1): Show | 4 | HG02055.hp2 HG03195.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.469+2332_469+2334d others(5): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112496706 | ||||||
chr2:112496708
|
T | TGTA | 4 | a0001c0001t0039g0028a0001c0001t0073g0020a0001c0001t0080g0020others(1): Show | 4 | HG01361.hp2 HG01981.hp2 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.469+2333_469+2334i others(5): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112496708 | ||||||
chr2:112496709
|
A | T | 6 | a0001c0001t0039g0028a0001c0001t0073g0020a0001c0001t0080g0020others(3): Show | 6 | HG01361.hp2 HG01981.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.469+2334A>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112496709 | ||||||
chr2:112496710
|
T | A | 58 | a0001c0001t0040g0046a0001c0002t0002g0003a0001c0002t0002g0008others(55): Show | 62 | HG00438.hp1 HG00621.hp1 HG00673.hp1 others(59): Show |
intron_variant | MODIFIER | c.469+2335T>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112496710 | ||||||
chr2:112496790
|
C | G | 7 | a0001c0002t0009g0143a0001c0002t0009g0144a0001c0002t0009g0294others(4): Show | 7 | HG01257.hp1 HG01258.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.469+2415C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112496790 | ||||||
chr2:112496815
|
C | T | 1 | a0001c0001t0069g0212 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.469+2440C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112496815 | ||||||
chr2:112496817
|
C | G | 7 | a0001c0002t0009g0143a0001c0002t0009g0144a0001c0002t0009g0294others(4): Show | 7 | HG01257.hp1 HG01258.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.469+2442C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112496817 | ||||||
chr2:112496946
|
G | A | 16 | a0001c0002t0006g0012a0001c0002t0006g0104a0001c0002t0006g0106others(13): Show | 17 | HG02572.hp2 HG02615.hp2 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.469+2571G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112496946 | ||||||
chr2:112497062
|
C | T | 177 | a0001c0001t0014g0030a0001c0001t0014g0031a0001c0001t0014g0033others(174): Show | 190 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.469+2687C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112497062 | ||||||
chr2:112497064
|
C | T | 2 | a0001c0002t0036g0301a0001c0002t0036g0302 | 2 | HG00438.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.469+2689C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112497064 | ||||||
chr2:112497121
|
C | T | 1 | a0001c0002t0042g0088 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.469+2746C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112497121 | ||||||
chr2:112497216
|
G | A | 1 | a0001c0002t0051g0237 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.469+2841G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112497216 | ||||||
chr2:112497292
|
C | T | 1 | a0001c0003t0003g0151 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.469+2917C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112497292 | ||||||
chr2:112497467
|
C | T | 75 | a0001c0002t0051g0237a0001c0002t0052g0236a0001c0003t0002g0170others(72): Show | 83 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.469+3092C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112497467 | ||||||
chr2:112497543
|
A | G | 1 | a0001c0002t0002g0121 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.469+3168A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112497543 | ||||||
chr2:112497629
|
G | A | 1 | a0001c0002t0042g0088 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.469+3254G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112497629 | ||||||
chr2:112497637
|
T | G | 172 | a0001c0002t0002g0003a0001c0002t0002g0008a0001c0002t0002g0013others(169): Show | 185 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.469+3262T>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112497637 | ||||||
chr2:112497760
|
A | G | 1 | a0001c0002t0057g0280 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.469+3385A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112497760 | ||||||
chr2:112497802
|
A | G | 1 | a0001c0001t0077g0292 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.470-3404A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112497802 | ||||||
chr2:112497840
|
C | T | 3 | a0001c0001t0001g0021a0001c0001t0001g0269a0001c0001t0001g0270 | 4 | HG01928.hp1 HG01993.hp1 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.470-3366C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112497840 | ||||||
chr2:112497920
|
A | G | 1 | a0001c0002t0008g0076 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.470-3286A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112497920 | ||||||
chr2:112497925
|
C | G | 1 | a0001c0002t0057g0280 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.470-3281C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112497925 | ||||||
chr2:112498269
|
G | A | 6 | a0001c0002t0020g0093a0001c0002t0028g0097a0001c0002t0028g0146others(3): Show | 6 | HG01891.hp1 HG02145.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.470-2937G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112498269 | ||||||
chr2:112498278
|
G | T | 1 | a0001c0002t0142g0095 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.470-2928G>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112498278 | ||||||
chr2:112498331
|
A | C | 19 | a0001c0001t0014g0030a0001c0001t0014g0031a0001c0001t0014g0033others(16): Show | 19 | HG01109.hp1 HG01257.hp1 HG01258.hp1 others(16): Show |
intron_variant | MODIFIER | c.470-2875A>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112498331 | ||||||
chr2:112498343
|
C | G | 2 | a0001c0002t0028g0097a0001c0002t0028g0146 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.470-2863C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112498343 | ||||||
chr2:112498484
|
C | T | 172 | a0001c0002t0002g0003a0001c0002t0002g0008a0001c0002t0002g0013others(169): Show | 185 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.470-2722C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112498484 | ||||||
chr2:112498570
|
T | C | 2 | a0001c0002t0127g0039a0001c0002t0129g0069 | 2 | HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.470-2636T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112498570 | ||||||
chr2:112498600
|
T | G | 1 | a0001c0002t0002g0122 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.470-2606T>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112498600 | ||||||
chr2:112498675
|
G | A | 2 | a0001c0001t0001g0265a0001c0002t0042g0088 | 2 | HG02132.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.470-2531G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112498675 | ||||||
chr2:112498719
|
C | T | 1 | a0001c0001t0014g0030 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.470-2487C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112498719 | ||||||
chr2:112498773
|
C | T | 12 | a0001c0002t0008g0070a0001c0002t0008g0072a0001c0002t0008g0074others(9): Show | 12 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(9): Show |
intron_variant | MODIFIER | c.470-2433C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112498773 | ||||||
chr2:112498777
|
C | T | 2 | a0001c0002t0009g0294a0001c0002t0009g0295 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.470-2429C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112498777 | ||||||
chr2:112498787
|
C | T | 1 | a0001c0002t0131g0034 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.470-2419C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112498787 | ||||||
chr2:112498838
|
C | T | 1 | a0001c0001t0007g0055 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.470-2368C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112498838 | ||||||
chr2:112498921
|
C | T | 73 | a0001c0003t0002g0170a0001c0003t0002g0172a0001c0003t0003g0004others(70): Show | 81 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.470-2285C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112498921 | ||||||
chr2:112499088
|
G | A | 1 | a0001c0001t0001g0255 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.470-2118G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112499088 | ||||||
chr2:112499184
|
G | A | 12 | a0001c0002t0002g0013a0001c0002t0002g0124a0001c0002t0002g0128others(9): Show | 13 | HG00438.hp1 HG02071.hp2 NA18939.hp1 others(10): Show |
intron_variant | MODIFIER | c.470-2022G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112499184 | ||||||
chr2:112499255
|
T | A | 8 | a0001c0002t0020g0093a0001c0002t0028g0097a0001c0002t0028g0146others(5): Show | 8 | HG01891.hp1 HG02145.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.470-1951T>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112499255 | ||||||
chr2:112499294
|
T | A | 1 | a0001c0001t0134g0029 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.470-1912T>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112499294 | ||||||
chr2:112499374
|
C | T | 8 | a0001c0002t0020g0093a0001c0002t0028g0097a0001c0002t0028g0146others(5): Show | 8 | HG01891.hp1 HG02145.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.470-1832C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112499374 | ||||||
chr2:112499398
|
G | A | 1 | a0001c0003t0004g0184 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.470-1808G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112499398 | ||||||
chr2:112499404
|
C | G | 16 | a0001c0002t0006g0012a0001c0002t0006g0104a0001c0002t0006g0106others(13): Show | 17 | HG02572.hp2 HG02615.hp2 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.470-1802C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112499404 | ||||||
chr2:112499705
|
A | T | 7 | a0001c0002t0009g0143a0001c0002t0009g0144a0001c0002t0009g0294others(4): Show | 7 | HG01257.hp1 HG01258.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.470-1501A>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112499705 | ||||||
chr2:112499880
|
G | C | 1 | a0001c0002t0057g0280 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.470-1326G>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112499880 | ||||||
chr2:112499950
|
A | G | 2 | a0001c0002t0127g0039a0001c0002t0129g0069 | 2 | HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.470-1256A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112499950 | ||||||
chr2:112500041
|
C | T | 1 | a0001c0001t0001g0278 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.470-1165C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112500041 | ||||||
chr2:112500139
|
A | G | 1 | a0001c0002t0002g0138 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.470-1067A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112500139 | ||||||
chr2:112500196
|
A | G | 2 | a0001c0002t0051g0237a0001c0002t0052g0236 | 2 | HG02896.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.470-1010A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112500196 | ||||||
chr2:112500235
|
G | A | 73 | a0001c0003t0002g0170a0001c0003t0002g0172a0001c0003t0003g0004others(70): Show | 81 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.470-971G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112500235 | ||||||
chr2:112500238
|
CA | C | 172 | a0001c0002t0002g0003a0001c0002t0002g0008a0001c0002t0002g0013others(169): Show | 185 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.470-966delA | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 112500238 | |||||
chr2:112500242
|
A | G | 3 | a0001c0003t0003g0174a0001c0003t0107g0173a0001c0003t0109g0175 | 3 | HG00639.hp2 HG01106.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.470-964A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112500242 | ||||||
chr2:112500527
|
C | T | 3 | a0001c0002t0015g0083a0001c0002t0015g0084a0001c0002t0015g0085 | 3 | HG02109.hp2 HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.470-679C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112500527 | ||||||
chr2:112500572
|
AAAAC | A | 5 | a0001c0001t0007g0051a0001c0001t0007g0052a0001c0001t0007g0053others(2): Show | 5 | HG00639.hp1 HG02717.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.470-618_470-615del others(4): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 112500572 | |||||
chr2:112500775
|
A | G | 1 | a0001c0002t0028g0097 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.470-431A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112500775 | ||||||
chr2:112500783
|
A | G | 8 | a0001c0002t0020g0093a0001c0002t0028g0097a0001c0002t0028g0146others(5): Show | 8 | HG01891.hp1 HG02145.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.470-423A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112500783 | ||||||
chr2:112500902
|
A | C | 81 | a0001c0001t0014g0030a0001c0001t0014g0031a0001c0001t0014g0033others(78): Show | 89 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.470-304A>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112500902 | ||||||
chr2:112501094
|
G | A | 172 | a0001c0002t0002g0003a0001c0002t0002g0008a0001c0002t0002g0013others(169): Show | 185 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.470-112G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 3/6 | chr2 | 112501094 | ||||||
chr2:112501371
|
T | C | 2 | a0001c0002t0127g0039a0001c0002t0129g0069 | 2 | HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.605+30T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 4/6 | chr2 | 112501371 | ||||||
chr2:112501498
|
C | T | 1 | a0001c0001t0132g0305 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.605+157C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 4/6 | chr2 | 112501498 | ||||||
chr2:112501641
|
A | G | 1 | a0001c0002t0008g0072 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.605+300A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 4/6 | chr2 | 112501641 | ||||||
chr2:112501642
|
T | C | 1 | a0001c0002t0008g0072 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.605+301T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 4/6 | chr2 | 112501642 | ||||||
chr2:112501643
|
G | A | 1 | a0001c0002t0008g0072 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.605+302G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 4/6 | chr2 | 112501643 | ||||||
chr2:112501782
|
A | T | 1 | a0001c0003t0106g0231 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.605+441A>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 4/6 | chr2 | 112501782 | ||||||
chr2:112501835
|
C | T | 1 | a0001c0002t0028g0146 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.605+494C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 4/6 | chr2 | 112501835 | ||||||
chr2:112501866
|
CA | C | 133 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0016others(130): Show | 146 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.605+544delA | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 112501866 | |||||
chr2:112501866
|
CAAAA | C | 162 | a0001c0002t0002g0003a0001c0002t0002g0008a0001c0002t0002g0013others(159): Show | 175 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.605+541_605+544del others(4): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 112501866 | |||||
chr2:112501866
|
CAAAAA | C | 8 | a0001c0002t0009g0143a0001c0002t0009g0144a0001c0002t0009g0294others(5): Show | 8 | HG01257.hp1 HG01258.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.605+540_605+544del others(5): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 112501866 | |||||
chr2:112501887
|
C | A | 7 | a0001c0002t0009g0143a0001c0002t0009g0144a0001c0002t0009g0294others(4): Show | 7 | HG01257.hp1 HG01258.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.605+546C>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 4/6 | chr2 | 112501887 | ||||||
chr2:112501896
|
A | G | 184 | a0001c0001t0014g0030a0001c0001t0014g0031a0001c0001t0014g0033others(181): Show | 197 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.605+555A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 4/6 | chr2 | 112501896 | ||||||
chr2:112501944
|
C | T | 1 | a0001c0001t0122g0102 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.605+603C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 4/6 | chr2 | 112501944 | ||||||
chr2:112502162
|
A | G | 66 | a0001c0002t0002g0003a0001c0002t0002g0008a0001c0002t0002g0013others(63): Show | 70 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.606-750A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 4/6 | chr2 | 112502162 | ||||||
chr2:112502637
|
C | CA | 15 | a0001c0001t0013g0047a0001c0001t0017g0250a0001c0001t0039g0028others(12): Show | 15 | HG01243.hp2 HG01361.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.606-259dupA | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 112502637 | |||||
chr2:112502637
|
CA | C | 76 | a0001c0001t0123g0098a0001c0002t0020g0093a0001c0002t0028g0097others(73): Show | 84 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.606-259delA | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 112502637 | |||||
chr2:112502661
|
AT | A | 172 | a0001c0002t0002g0003a0001c0002t0002g0008a0001c0002t0002g0013others(169): Show | 185 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.606-244delT | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 112502661 | |||||
chr2:112502872
|
T | C | 1 | a0001c0002t0002g0131 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.606-40T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 4/6 | chr2 | 112502872 | ||||||
chr2:112503284
|
T | G | 97 | a0001c0002t0002g0003a0001c0002t0002g0008a0001c0002t0002g0013others(94): Show | 102 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.875+103T>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112503284 | ||||||
chr2:112503387
|
A | ATG | 17 | a0001c0001t0135g0024a0001c0002t0006g0012a0001c0002t0006g0104others(14): Show | 18 | HG02572.hp2 HG02602.hp2 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.875+222_875+223dup others(2): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112503387 | |||||
chr2:112503387
|
A | G | 1 | a0001c0002t0142g0095 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.875+206A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112503387 | ||||||
chr2:112503401
|
G | A | 1 | a0001c0002t0057g0280 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.875+220G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112503401 | ||||||
chr2:112503401
|
G | GTA | 12 | a0001c0002t0008g0070a0001c0002t0008g0072a0001c0002t0008g0074others(9): Show | 12 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(9): Show |
intron_variant | MODIFIER | c.875+221_875+222ins others(2): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112503401 | |||||
chr2:112503401
|
G | GTATA | 5 | a0001c0002t0020g0093a0001c0002t0028g0097a0001c0002t0028g0146others(2): Show | 5 | HG01891.hp1 HG03098.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.875+221_875+222ins others(4): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112503401 | |||||
chr2:112503403
|
G | A | 20 | a0001c0002t0008g0070a0001c0002t0008g0072a0001c0002t0008g0074others(17): Show | 20 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(17): Show |
intron_variant | MODIFIER | c.875+222G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112503403 | ||||||
chr2:112503403
|
G | GTA | 8 | a0001c0001t0030g0258a0001c0002t0009g0143a0001c0002t0009g0144others(5): Show | 8 | HG00140.hp2 HG01257.hp1 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.875+238_875+239dup others(2): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112503403 | |||||
chr2:112503403
|
G | GTATA | 54 | a0001c0001t0069g0212a0001c0001t0079g0257a0001c0002t0002g0003others(51): Show | 59 | HG00438.hp1 HG00621.hp1 HG00673.hp1 others(56): Show |
intron_variant | MODIFIER | c.875+236_875+239dup others(4): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112503403 | |||||
chr2:112503403
|
G | GTATATA | 60 | a0001c0002t0002g0079a0001c0002t0002g0080a0001c0002t0002g0132others(57): Show | 67 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.875+234_875+239dup others(6): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112503403 | |||||
chr2:112503403
|
G | GTATATAT others(1): Show |
6 | a0001c0003t0003g0242a0001c0003t0010g0065a0001c0003t0011g0298others(3): Show | 6 | HG02055.hp2 HG02083.hp1 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.875+232_875+239dup others(8): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112503403 | |||||
chr2:112503403
|
G | GTATATAT others(3): Show |
1 | a0001c0003t0020g0177 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.875+230_875+239dup others(10): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112503403 | |||||
chr2:112503403
|
G | GTGTATA | 4 | a0001c0003t0003g0151a0001c0003t0004g0113a0001c0003t0021g0165others(1): Show | 4 | HG02280.hp2 HG03239.hp1 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.875+223_875+224ins others(6): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112503403 | |||||
chr2:112503403
|
G | GTGTATAT others(1): Show |
4 | a0001c0003t0003g0230a0001c0003t0010g0010a0001c0003t0010g0064others(1): Show | 4 | NA18945.hp2 NA18957.hp1 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.875+223_875+224ins others(8): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112503403 | |||||
chr2:112503403
|
GTA | G | 3 | a0001c0001t0032g0192a0001c0001t0032g0193a0001c0001t0097g0211 | 3 | HG01175.hp1 HG02630.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.875+238_875+239del others(2): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112503403 | |||||
chr2:112503405
|
A | G | 12 | a0001c0001t0014g0030a0001c0001t0014g0031a0001c0001t0014g0033others(9): Show | 12 | HG01109.hp1 HG01346.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.875+224A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112503405 | ||||||
chr2:112503429
|
T | A | 17 | a0001c0002t0006g0012a0001c0002t0006g0104a0001c0002t0006g0106others(14): Show | 18 | HG02572.hp2 HG02615.hp2 HG02622.hp1 others(15): Show |
intron_variant | MODIFIER | c.875+248T>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112503429 | ||||||
chr2:112503458
|
A | G | 97 | a0001c0002t0002g0003a0001c0002t0002g0008a0001c0002t0002g0013others(94): Show | 102 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.875+277A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112503458 | ||||||
chr2:112503483
|
G | C | 1 | a0001c0001t0001g0273 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.875+302G>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112503483 | ||||||
chr2:112503490
|
A | G | 2 | a0001c0002t0026g0059a0001c0002t0041g0058 | 2 | HG01074.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.875+309A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112503490 | ||||||
chr2:112503577
|
G | A | 1 | a0001c0002t0142g0095 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.875+396G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112503577 | ||||||
chr2:112503658
|
C | CT | 15 | a0001c0001t0014g0033a0001c0002t0008g0070a0001c0002t0008g0072others(12): Show | 15 | HG00140.hp1 HG00280.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.875+497dupT | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112503658 | |||||
chr2:112503658
|
CT | C | 101 | a0001c0001t0013g0049a0001c0001t0016g0194a0001c0001t0040g0046others(98): Show | 110 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.875+497delT | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112503658 | |||||
chr2:112503658
|
CTT | C | 6 | a0001c0002t0012g0112a0001c0002t0051g0237a0001c0002t0127g0039others(3): Show | 6 | HG02647.hp2 HG02723.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.875+496_875+497del others(2): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112503658 | |||||
chr2:112503700
|
TA | T | 73 | a0001c0003t0002g0170a0001c0003t0002g0172a0001c0003t0003g0004others(70): Show | 81 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.875+520delA | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112503700 | ||||||
chr2:112503775
|
T | G | 1 | a0001c0001t0082g0259 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.875+594T>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112503775 | ||||||
chr2:112503805
|
C | CT | 131 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0016others(128): Show | 141 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.875+644dupT | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112503805 | |||||
chr2:112503805
|
CT | C | 77 | a0001c0002t0006g0107a0001c0002t0012g0105a0001c0002t0042g0088others(74): Show | 85 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.875+644delT | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112503805 | |||||
chr2:112503805
|
CTT | C | 7 | a0001c0002t0020g0093a0001c0002t0028g0097a0001c0002t0028g0146others(4): Show | 7 | HG01891.hp1 HG02280.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.875+643_875+644del others(2): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112503805 | |||||
chr2:112503805
|
CTTT | C | 49 | a0001c0002t0002g0003a0001c0002t0002g0008a0001c0002t0002g0013others(46): Show | 53 | HG00438.hp1 HG00621.hp1 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.875+642_875+644del others(3): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112503805 | |||||
chr2:112503805
|
CTTTTT | C | 11 | a0001c0002t0008g0070a0001c0002t0008g0074a0001c0002t0008g0075others(8): Show | 11 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(8): Show |
intron_variant | MODIFIER | c.875+640_875+644del others(5): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112503805 | |||||
chr2:112503902
|
C | T | 1 | a0001c0001t0001g0255 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.875+721C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112503902 | ||||||
chr2:112503962
|
C | A | 75 | a0001c0002t0051g0237a0001c0002t0052g0236a0001c0003t0002g0170others(72): Show | 83 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.875+781C>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112503962 | ||||||
chr2:112503997
|
T | C | 1 | a0001c0001t0126g0035 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.875+816T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112503997 | ||||||
chr2:112504082
|
C | T | 7 | a0001c0002t0006g0104a0001c0002t0006g0106a0001c0002t0006g0110others(4): Show | 7 | HG02572.hp2 HG02615.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.875+901C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112504082 | ||||||
chr2:112504107
|
T | G | 1 | a0001c0001t0096g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.875+926T>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112504107 | ||||||
chr2:112504111
|
A | G | 66 | a0001c0002t0002g0003a0001c0002t0002g0008a0001c0002t0002g0013others(63): Show | 70 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.875+930A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112504111 | ||||||
chr2:112504182
|
A | G | 98 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0016others(95): Show | 107 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.875+1001A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112504182 | ||||||
chr2:112504286
|
G | A | 12 | a0001c0002t0008g0070a0001c0002t0008g0072a0001c0002t0008g0074others(9): Show | 12 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(9): Show |
intron_variant | MODIFIER | c.875+1105G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112504286 | ||||||
chr2:112504349
|
A | C | 1 | a0001c0002t0002g0131 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.875+1168A>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112504349 | ||||||
chr2:112504383
|
C | T | 1 | a0001c0001t0085g0145 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.875+1202C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112504383 | ||||||
chr2:112504449
|
A | G | 1 | a0001c0003t0004g0162 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.875+1268A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112504449 | ||||||
chr2:112504513
|
G | A | 91 | a0001c0002t0002g0003a0001c0002t0002g0008a0001c0002t0002g0013others(88): Show | 96 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.875+1332G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112504513 | ||||||
chr2:112504522
|
G | A | 1 | a0001c0003t0111g0154 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.875+1341G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112504522 | ||||||
chr2:112504738
|
C | T | 55 | a0001c0001t0070g0082a0001c0002t0002g0003a0001c0002t0002g0008others(52): Show | 59 | HG00438.hp1 HG00621.hp1 HG00673.hp1 others(56): Show |
intron_variant | MODIFIER | c.875+1557C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112504738 | ||||||
chr2:112504739
|
G | A | 37 | a0001c0002t0006g0012a0001c0002t0006g0104a0001c0002t0006g0106others(34): Show | 38 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(35): Show |
intron_variant | MODIFIER | c.875+1558G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112504739 | ||||||
chr2:112504818
|
A | G | 12 | a0001c0002t0008g0070a0001c0002t0008g0072a0001c0002t0008g0074others(9): Show | 12 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(9): Show |
intron_variant | MODIFIER | c.875+1637A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112504818 | ||||||
chr2:112504820
|
G | T | 184 | a0001c0001t0014g0030a0001c0001t0014g0031a0001c0001t0014g0033others(181): Show | 197 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.875+1639G>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112504820 | ||||||
chr2:112504842
|
G | T | 172 | a0001c0002t0002g0003a0001c0002t0002g0008a0001c0002t0002g0013others(169): Show | 185 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.875+1661G>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112504842 | ||||||
chr2:112505168
|
A | G | 54 | a0001c0002t0002g0003a0001c0002t0002g0008a0001c0002t0002g0013others(51): Show | 58 | HG00438.hp1 HG00621.hp1 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.875+1987A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112505168 | ||||||
chr2:112505246
|
T | G | 1 | a0001c0003t0104g0163 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.875+2065T>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112505246 | ||||||
chr2:112505284
|
A | T | 1 | a0002c0005t0019g0137 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.875+2103A>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112505284 | ||||||
chr2:112505290
|
C | T | 1 | a0001c0001t0093g0240 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.875+2109C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112505290 | ||||||
chr2:112505310
|
T | C | 97 | a0001c0002t0002g0003a0001c0002t0002g0008a0001c0002t0002g0013others(94): Show | 102 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.875+2129T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112505310 | ||||||
chr2:112505390
|
G | A | 1 | a0001c0002t0055g0279 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.875+2209G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112505390 | ||||||
chr2:112505497
|
G | T | 1 | a0001c0003t0003g0229 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.875+2316G>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112505497 | ||||||
chr2:112505515
|
T | G | 2 | a0001c0001t0076g0090a0001c0001t0090g0293 | 2 | HG02922.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.875+2334T>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112505515 | ||||||
chr2:112505567
|
C | T | 1 | a0001c0001t0086g0114 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.875+2386C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112505567 | ||||||
chr2:112505580
|
G | A | 1 | a0001c0002t0057g0280 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.875+2399G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112505580 | ||||||
chr2:112505595
|
C | G | 1 | a0001c0002t0142g0095 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.875+2414C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112505595 | ||||||
chr2:112505611
|
CTGTT | C | 75 | a0001c0002t0051g0237a0001c0002t0052g0236a0001c0003t0002g0170others(72): Show | 83 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.875+2434_875+2437d others(6): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112505611 | |||||
chr2:112505712
|
T | G | 1 | a0001c0001t0007g0055 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.875+2531T>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112505712 | ||||||
chr2:112505738
|
A | G | 1 | a0001c0001t0001g0197 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.875+2557A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112505738 | ||||||
chr2:112505753
|
G | A | 75 | a0001c0002t0051g0237a0001c0002t0052g0236a0001c0003t0002g0170others(72): Show | 83 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.875+2572G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112505753 | ||||||
chr2:112505846
|
T | C | 172 | a0001c0002t0002g0003a0001c0002t0002g0008a0001c0002t0002g0013others(169): Show | 185 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.875+2665T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112505846 | ||||||
chr2:112505864
|
C | T | 56 | a0001c0002t0002g0003a0001c0002t0002g0008a0001c0002t0002g0013others(53): Show | 60 | HG00438.hp1 HG00621.hp1 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.875+2683C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112505864 | ||||||
chr2:112505977
|
T | A | 1 | a0001c0002t0116g0289 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.875+2796T>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112505977 | ||||||
chr2:112506103
|
T | C | 94 | a0001c0002t0002g0003a0001c0002t0002g0008a0001c0002t0002g0013others(91): Show | 99 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.875+2922T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112506103 | ||||||
chr2:112506299
|
C | A | 18 | a0001c0002t0006g0012a0001c0002t0006g0104a0001c0002t0006g0106others(15): Show | 19 | HG02572.hp2 HG02615.hp2 HG02622.hp1 others(16): Show |
intron_variant | MODIFIER | c.875+3118C>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112506299 | ||||||
chr2:112506299
|
C | T | 11 | a0001c0002t0008g0070a0001c0002t0008g0074a0001c0002t0008g0075others(8): Show | 11 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(8): Show |
intron_variant | MODIFIER | c.875+3118C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112506299 | ||||||
chr2:112506423
|
T | C | 79 | a0001c0002t0002g0003a0001c0002t0002g0008a0001c0002t0002g0013others(76): Show | 83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.875+3242T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112506423 | ||||||
chr2:112506424
|
C | T | 78 | a0001c0002t0006g0104a0001c0002t0006g0106a0001c0002t0006g0110others(75): Show | 86 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.875+3243C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112506424 | ||||||
chr2:112506429
|
G | T | 16 | a0001c0002t0006g0012a0001c0002t0006g0104a0001c0002t0006g0106others(13): Show | 17 | HG02572.hp2 HG02615.hp2 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.875+3248G>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112506429 | ||||||
chr2:112506522
|
A | G | 75 | a0001c0002t0051g0237a0001c0002t0052g0236a0001c0003t0002g0170others(72): Show | 83 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.875+3341A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112506522 | ||||||
chr2:112506599
|
T | A | 1 | a0001c0001t0001g0197 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.875+3418T>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112506599 | ||||||
chr2:112506616
|
A | C | 3 | a0001c0001t0025g0009a0001c0001t0025g0042a0001c0001t0134g0029 | 4 | HG00738.hp2 HG01256.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.875+3435A>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112506616 | ||||||
chr2:112506652
|
C | T | 1 | a0001c0001t0026g0056 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.875+3471C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112506652 | ||||||
chr2:112506693
|
T | A | 8 | a0001c0001t0014g0030a0001c0001t0014g0031a0001c0001t0014g0033others(5): Show | 8 | HG01109.hp1 HG01346.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.875+3512T>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112506693 | ||||||
chr2:112506703
|
C | G | 12 | a0001c0002t0008g0070a0001c0002t0008g0072a0001c0002t0008g0074others(9): Show | 12 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(9): Show |
intron_variant | MODIFIER | c.875+3522C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112506703 | ||||||
chr2:112506731
|
C | T | 8 | a0001c0001t0014g0030a0001c0001t0014g0031a0001c0001t0014g0033others(5): Show | 8 | HG01109.hp1 HG01346.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.875+3550C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112506731 | ||||||
chr2:112506757
|
G | C | 172 | a0001c0002t0002g0003a0001c0002t0002g0008a0001c0002t0002g0013others(169): Show | 185 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.875+3576G>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112506757 | ||||||
chr2:112506833
|
T | G | 1 | a0001c0002t0142g0095 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.875+3652T>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112506833 | ||||||
chr2:112506945
|
A | G | 97 | a0001c0002t0002g0003a0001c0002t0002g0008a0001c0002t0002g0013others(94): Show | 102 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.875+3764A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112506945 | ||||||
chr2:112506974
|
C | A | 14 | a0001c0002t0006g0012a0001c0002t0006g0104a0001c0002t0006g0106others(11): Show | 15 | HG02572.hp2 HG02615.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.875+3793C>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112506974 | ||||||
chr2:112506987
|
A | G | 1 | a0001c0003t0020g0177 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.875+3806A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112506987 | ||||||
chr2:112507012
|
G | T | 2 | a0001c0001t0001g0210a0001c0002t0042g0088 | 2 | HG03927.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.875+3831G>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112507012 | ||||||
chr2:112507027
|
A | G | 172 | a0001c0002t0002g0003a0001c0002t0002g0008a0001c0002t0002g0013others(169): Show | 185 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.875+3846A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112507027 | ||||||
chr2:112507053
|
C | T | 1 | a0001c0003t0021g0171 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.875+3872C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112507053 | ||||||
chr2:112507103
|
A | T | 1 | a0001c0002t0008g0075 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.875+3922A>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112507103 | ||||||
chr2:112507118
|
G | A | 1 | a0001c0002t0008g0089 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.875+3937G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112507118 | ||||||
chr2:112507223
|
G | A | 1 | a0001c0001t0082g0259 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.875+4042G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112507223 | ||||||
chr2:112507286
|
T | G | 2 | a0001c0001t0031g0290a0001c0001t0072g0253 | 2 | HG02083.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.875+4105T>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112507286 | ||||||
chr2:112507388
|
G | A | 1 | a0001c0003t0118g0155 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.875+4207G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112507388 | ||||||
chr2:112507602
|
A | G | 172 | a0001c0002t0002g0003a0001c0002t0002g0008a0001c0002t0002g0013others(169): Show | 185 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.875+4421A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112507602 | ||||||
chr2:112507769
|
A | G | 2 | a0001c0003t0105g0147a0001c0003t0137g0026 | 2 | HG01074.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.875+4588A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112507769 | ||||||
chr2:112507856
|
T | G | 6 | a0001c0002t0020g0093a0001c0002t0028g0097a0001c0002t0028g0146others(3): Show | 6 | HG01891.hp1 HG02145.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.875+4675T>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112507856 | ||||||
chr2:112507943
|
T | C | 97 | a0001c0002t0002g0003a0001c0002t0002g0008a0001c0002t0002g0013others(94): Show | 102 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.875+4762T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112507943 | ||||||
chr2:112508161
|
G | T | 2 | a0001c0002t0009g0143a0001c0002t0009g0144 | 2 | HG01884.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.875+4980G>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112508161 | ||||||
chr2:112508172
|
G | C | 1 | a0001c0002t0002g0140 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.875+4991G>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112508172 | ||||||
chr2:112508175
|
G | A | 16 | a0001c0002t0006g0012a0001c0002t0006g0104a0001c0002t0006g0106others(13): Show | 17 | HG02572.hp2 HG02615.hp2 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.875+4994G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112508175 | ||||||
chr2:112508306
|
T | C | 3 | a0001c0002t0029g0187a0001c0002t0029g0188a0001c0002t0128g0040 | 3 | HG01243.hp2 HG02895.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.875+5125T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112508306 | ||||||
chr2:112508321
|
T | C | 2 | a0001c0001t0076g0090a0001c0001t0090g0293 | 2 | HG02922.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.875+5140T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112508321 | ||||||
chr2:112508456
|
C | G | 1 | a0001c0002t0042g0088 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.875+5275C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112508456 | ||||||
chr2:112508607
|
C | T | 2 | a0001c0001t0048g0275a0001c0001t0050g0276 | 2 | HG01346.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.875+5426C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112508607 | ||||||
chr2:112508615
|
G | C | 7 | a0001c0002t0009g0143a0001c0002t0009g0144a0001c0002t0009g0294others(4): Show | 7 | HG01257.hp1 HG01258.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.875+5434G>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112508615 | ||||||
chr2:112508635
|
G | A | 2 | a0001c0002t0016g0123a0001c0002t0016g0127 | 2 | NA18943.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.875+5454G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112508635 | ||||||
chr2:112508643
|
C | T | 96 | a0001c0002t0002g0003a0001c0002t0002g0008a0001c0002t0002g0013others(93): Show | 101 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.875+5462C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112508643 | ||||||
chr2:112508666
|
C | G | 116 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0016others(113): Show | 126 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.875+5485C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112508666 | ||||||
chr2:112508686
|
C | G | 16 | a0001c0002t0006g0012a0001c0002t0006g0104a0001c0002t0006g0106others(13): Show | 17 | HG02572.hp2 HG02615.hp2 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.875+5505C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112508686 | ||||||
chr2:112508770
|
G | A | 73 | a0001c0003t0002g0170a0001c0003t0002g0172a0001c0003t0003g0004others(70): Show | 81 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.875+5589G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112508770 | ||||||
chr2:112508998
|
A | G | 1 | a0001c0001t0001g0205 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.875+5817A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112508998 | ||||||
chr2:112509014
|
TGTTA | T | 54 | a0001c0002t0002g0003a0001c0002t0002g0008a0001c0002t0002g0013others(51): Show | 58 | HG00438.hp1 HG00621.hp1 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.875+5837_875+5840d others(6): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112509014 | |||||
chr2:112509073
|
T | C | 186 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0019others(183): Show | 201 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.875+5892T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112509073 | ||||||
chr2:112509093
|
C | G | 1 | a0001c0001t0001g0252 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.875+5912C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112509093 | ||||||
chr2:112509100
|
T | G | 183 | a0001c0001t0014g0030a0001c0001t0014g0031a0001c0001t0014g0033others(180): Show | 196 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.875+5919T>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112509100 | ||||||
chr2:112509102
|
G | A | 12 | a0001c0001t0014g0030a0001c0001t0014g0031a0001c0001t0014g0033others(9): Show | 12 | HG01109.hp1 HG01346.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.875+5921G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112509102 | ||||||
chr2:112509169
|
C | G | 1 | a0001c0001t0001g0077 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.875+5988C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112509169 | ||||||
chr2:112509169
|
C | T | 1 | a0001c0001t0100g0103 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.875+5988C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112509169 | ||||||
chr2:112509170
|
G | A | 2 | a0001c0003t0011g0023a0001c0003t0011g0300 | 3 | NA18960.hp2 NA18964.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.875+5989G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112509170 | ||||||
chr2:112509240
|
A | G | 51 | a0001c0002t0002g0003a0001c0002t0002g0008a0001c0002t0002g0013others(48): Show | 55 | HG00438.hp1 HG00621.hp1 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.875+6059A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112509240 | ||||||
chr2:112509349
|
C | G | 55 | a0001c0001t0030g0244a0001c0002t0002g0003a0001c0002t0002g0008others(52): Show | 59 | HG00438.hp1 HG00621.hp1 HG00673.hp1 others(56): Show |
intron_variant | MODIFIER | c.875+6168C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112509349 | ||||||
chr2:112509358
|
T | C | 1 | a0001c0002t0002g0281 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.875+6177T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112509358 | ||||||
chr2:112509383
|
C | G | 1 | a0001c0001t0001g0254 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.875+6202C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112509383 | ||||||
chr2:112509418
|
T | C | 54 | a0001c0002t0002g0003a0001c0002t0002g0008a0001c0002t0002g0013others(51): Show | 58 | HG00438.hp1 HG00621.hp1 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.875+6237T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112509418 | ||||||
chr2:112509496
|
G | T | 2 | a0001c0001t0024g0007a0001c0001t0122g0102 | 4 | HG01167.hp2 HG02723.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.875+6315G>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112509496 | ||||||
chr2:112509547
|
C | T | 11 | a0001c0002t0008g0070a0001c0002t0008g0072a0001c0002t0008g0074others(8): Show | 11 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(8): Show |
intron_variant | MODIFIER | c.875+6366C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112509547 | ||||||
chr2:112509550
|
A | G | 2 | a0001c0002t0002g0135a0001c0002t0002g0136 | 2 | HG03710.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.875+6369A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112509550 | ||||||
chr2:112509560
|
T | C | 1 | a0001c0003t0035g0156 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.875+6379T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112509560 | ||||||
chr2:112509589
|
T | C | 97 | a0001c0002t0002g0003a0001c0002t0002g0008a0001c0002t0002g0013others(94): Show | 102 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.875+6408T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112509589 | ||||||
chr2:112509660
|
G | A | 1 | a0001c0001t0091g0219 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.875+6479G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112509660 | ||||||
chr2:112509663
|
C | G | 1 | a0001c0002t0142g0095 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.875+6482C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112509663 | ||||||
chr2:112509669
|
C | T | 2 | a0001c0001t0007g0037a0001c0001t0007g0038 | 2 | HG02258.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.875+6488C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112509669 | ||||||
chr2:112509674
|
C | T | 1 | a0001c0002t0142g0095 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.875+6493C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112509674 | ||||||
chr2:112509702
|
G | C | 5 | a0001c0002t0002g0008a0001c0002t0002g0122a0001c0002t0002g0182others(2): Show | 7 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.875+6521G>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112509702 | ||||||
chr2:112509774
|
C | T | 1 | a0001c0001t0017g0204 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.875+6593C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112509774 | ||||||
chr2:112509793
|
G | T | 1 | a0001c0002t0042g0088 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.875+6612G>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112509793 | ||||||
chr2:112509861
|
T | C | 1 | a0001c0003t0037g0157 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.875+6680T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112509861 | ||||||
chr2:112509886
|
G | A | 16 | a0001c0002t0006g0012a0001c0002t0006g0104a0001c0002t0006g0106others(13): Show | 17 | HG02572.hp2 HG02615.hp2 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.875+6705G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112509886 | ||||||
chr2:112509914
|
G | A | 1 | a0001c0001t0031g0267 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.875+6733G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112509914 | ||||||
chr2:112509923
|
C | T | 8 | a0001c0001t0007g0051a0001c0001t0007g0052a0001c0001t0007g0053others(5): Show | 8 | HG00639.hp1 HG02717.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.875+6742C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112509923 | ||||||
chr2:112509963
|
A | G | 1 | a0001c0001t0001g0191 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.875+6782A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112509963 | ||||||
chr2:112509964
|
C | G | 1 | a0001c0002t0008g0076 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.875+6783C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112509964 | ||||||
chr2:112510228
|
C | T | 1 | a0001c0002t0045g0081 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.875+7047C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112510228 | ||||||
chr2:112510319
|
G | T | 16 | a0001c0002t0006g0012a0001c0002t0006g0104a0001c0002t0006g0106others(13): Show | 17 | HG02572.hp2 HG02615.hp2 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.875+7138G>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112510319 | ||||||
chr2:112510352
|
C | T | 1 | a0001c0001t0063g0209 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.875+7171C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112510352 | ||||||
chr2:112510507
|
T | C | 16 | a0001c0002t0006g0012a0001c0002t0006g0104a0001c0002t0006g0106others(13): Show | 17 | HG02572.hp2 HG02615.hp2 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.875+7326T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112510507 | ||||||
chr2:112510541
|
G | A | 1 | a0001c0003t0137g0026 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.875+7360G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112510541 | ||||||
chr2:112510659
|
C | T | 4 | a0001c0001t0014g0031a0001c0001t0014g0033a0001c0001t0014g0044others(1): Show | 4 | HG01109.hp1 HG02055.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.875+7478C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112510659 | ||||||
chr2:112510824
|
C | G | 1 | a0001c0002t0131g0034 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.875+7643C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112510824 | ||||||
chr2:112510828
|
A | G | 1 | a0001c0002t0056g0094 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.875+7647A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112510828 | ||||||
chr2:112510940
|
A | T | 2 | a0001c0001t0001g0247a0001c0001t0001g0278 | 2 | HG01256.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.875+7759A>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112510940 | ||||||
chr2:112510943
|
G | T | 1 | a0001c0003t0138g0025 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.875+7762G>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112510943 | ||||||
chr2:112511091
|
T | C | 172 | a0001c0002t0002g0003a0001c0002t0002g0008a0001c0002t0002g0013others(169): Show | 185 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.875+7910T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112511091 | ||||||
chr2:112511319
|
T | C | 2 | a0001c0002t0002g0079a0001c0002t0002g0080 | 2 | HG02132.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.875+8138T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112511319 | ||||||
chr2:112511470
|
T | G | 2 | a0001c0002t0053g0233a0001c0002t0054g0234 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.875+8289T>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112511470 | ||||||
chr2:112511506
|
A | G | 1 | a0001c0002t0042g0088 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.875+8325A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112511506 | ||||||
chr2:112511611
|
C | T | 16 | a0001c0002t0006g0012a0001c0002t0006g0104a0001c0002t0006g0106others(13): Show | 17 | HG02572.hp2 HG02615.hp2 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.875+8430C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112511611 | ||||||
chr2:112511754
|
A | G | 1 | a0001c0003t0037g0161 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.876-8528A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112511754 | ||||||
chr2:112511817
|
C | T | 1 | a0001c0001t0120g0100 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.876-8465C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112511817 | ||||||
chr2:112511823
|
A | G | 54 | a0001c0002t0002g0003a0001c0002t0002g0008a0001c0002t0002g0013others(51): Show | 58 | HG00438.hp1 HG00621.hp1 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.876-8459A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112511823 | ||||||
chr2:112511982
|
C | CATTCT | 95 | a0001c0001t0001g0272a0001c0002t0002g0003a0001c0002t0002g0008others(92): Show | 100 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.876-8282_876-8278d others(7): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112511982 | |||||
chr2:112511982
|
C | CATTCTAT others(3): Show |
1 | a0001c0002t0002g0129 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.876-8287_876-8278d others(12): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112511982 | |||||
chr2:112512027
|
T | C | 3 | a0001c0003t0003g0174a0001c0003t0107g0173a0001c0003t0109g0175 | 3 | HG00639.hp2 HG01106.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.876-8255T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112512027 | ||||||
chr2:112512057
|
A | T | 1 | a0001c0002t0056g0094 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.876-8225A>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112512057 | ||||||
chr2:112512129
|
C | T | 172 | a0001c0002t0002g0003a0001c0002t0002g0008a0001c0002t0002g0013others(169): Show | 185 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.876-8153C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112512129 | ||||||
chr2:112512324
|
G | A | 12 | a0001c0002t0008g0070a0001c0002t0008g0072a0001c0002t0008g0074others(9): Show | 12 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(9): Show |
intron_variant | MODIFIER | c.876-7958G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112512324 | ||||||
chr2:112512331
|
C | T | 1 | a0001c0001t0085g0145 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.876-7951C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112512331 | ||||||
chr2:112512339
|
T | G | 1 | a0001c0002t0042g0088 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.876-7943T>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112512339 | ||||||
chr2:112512348
|
C | T | 7 | a0001c0002t0009g0143a0001c0002t0009g0144a0001c0002t0009g0294others(4): Show | 7 | HG01257.hp1 HG01258.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.876-7934C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112512348 | ||||||
chr2:112512407
|
C | T | 2 | a0001c0001t0001g0191a0001c0001t0001g0203 | 2 | NA19080.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.876-7875C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112512407 | ||||||
chr2:112512484
|
G | A | 1 | a0001c0001t0001g0196 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.876-7798G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112512484 | ||||||
chr2:112512514
|
G | A | 1 | a0001c0002t0140g0045 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.876-7768G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112512514 | ||||||
chr2:112512625
|
G | A | 1 | a0001c0001t0001g0210 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.876-7657G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112512625 | ||||||
chr2:112512643
|
C | T | 54 | a0001c0002t0002g0003a0001c0002t0002g0008a0001c0002t0002g0013others(51): Show | 58 | HG00438.hp1 HG00621.hp1 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.876-7639C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112512643 | ||||||
chr2:112512657
|
A | G | 1 | a0001c0001t0001g0222 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.876-7625A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112512657 | ||||||
chr2:112512787
|
C | T | 12 | a0001c0001t0014g0030a0001c0001t0014g0031a0001c0001t0014g0033others(9): Show | 12 | HG01109.hp1 HG01346.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.876-7495C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112512787 | ||||||
chr2:112512937
|
G | A | 1 | a0001c0002t0057g0280 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.876-7345G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112512937 | ||||||
chr2:112513022
|
G | A | 54 | a0001c0002t0002g0003a0001c0002t0002g0008a0001c0002t0002g0013others(51): Show | 58 | HG00438.hp1 HG00621.hp1 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.876-7260G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112513022 | ||||||
chr2:112513172
|
A | G | 3 | a0001c0002t0029g0187a0001c0002t0029g0188a0001c0002t0128g0040 | 3 | HG01243.hp2 HG02895.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.876-7110A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112513172 | ||||||
chr2:112513215
|
G | A | 54 | a0001c0002t0002g0003a0001c0002t0002g0008a0001c0002t0002g0013others(51): Show | 58 | HG00438.hp1 HG00621.hp1 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.876-7067G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112513215 | ||||||
chr2:112513337
|
C | T | 75 | a0001c0002t0051g0237a0001c0002t0052g0236a0001c0003t0002g0170others(72): Show | 83 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.876-6945C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112513337 | ||||||
chr2:112513452
|
A | G | 1 | a0001c0003t0021g0165 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.876-6830A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112513452 | ||||||
chr2:112513457
|
T | C | 1 | a0001c0001t0123g0098 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.876-6825T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112513457 | ||||||
chr2:112513541
|
G | T | 3 | a0001c0002t0015g0083a0001c0002t0015g0084a0001c0002t0015g0085 | 3 | HG02109.hp2 HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.876-6741G>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112513541 | ||||||
chr2:112513569
|
A | G | 16 | a0001c0002t0006g0012a0001c0002t0006g0104a0001c0002t0006g0106others(13): Show | 17 | HG02572.hp2 HG02615.hp2 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.876-6713A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112513569 | ||||||
chr2:112513571
|
A | ATATAAAT others(35): Show |
3 | a0001c0002t0022g0126a0001c0003t0003g0151a0001c0003t0004g0113 | 3 | NA18964.hp1 NA19066.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.876-6689_876-6648d others(44): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112513571 | |||||
chr2:112513575
|
AAATATTT others(53): Show |
A | 2 | a0001c0002t0051g0237a0001c0002t0052g0236 | 2 | HG02896.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.876-6683_876-6624d others(62): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112513575 | |||||
chr2:112513587
|
A | T | 1 | a0001c0003t0035g0156 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.876-6695A>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112513587 | ||||||
chr2:112513617
|
AAATATTT others(11): Show |
A | 1 | a0001c0003t0112g0149 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.876-6647_876-6630d others(20): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112513617 | |||||
chr2:112513626
|
T | C | 2 | a0001c0001t0025g0009a0001c0001t0025g0042 | 3 | HG00738.hp2 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.876-6656T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112513626 | ||||||
chr2:112513628
|
C | CAAGTATA others(17): Show |
1 | a0001c0002t0142g0095 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.876-6648_876-6647i others(26): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112513628 | |||||
chr2:112513635
|
G | A | 181 | a0001c0001t0014g0030a0001c0001t0014g0031a0001c0001t0014g0033others(178): Show | 194 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.876-6647G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112513635 | ||||||
chr2:112513817
|
G | T | 1 | a0001c0001t0001g0269 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.876-6465G>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112513817 | ||||||
chr2:112513832
|
C | A | 172 | a0001c0002t0002g0003a0001c0002t0002g0008a0001c0002t0002g0013others(169): Show | 185 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.876-6450C>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112513832 | ||||||
chr2:112513879
|
G | T | 1 | a0001c0002t0002g0131 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.876-6403G>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112513879 | ||||||
chr2:112513929
|
A | G | 1 | a0001c0002t0045g0081 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.876-6353A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112513929 | ||||||
chr2:112514110
|
G | A | 3 | a0001c0001t0001g0087a0001c0003t0003g0151a0001c0003t0004g0113 | 3 | HG01516.hp2 NA19066.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.876-6172G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112514110 | ||||||
chr2:112514227
|
G | A | 16 | a0001c0002t0006g0012a0001c0002t0006g0104a0001c0002t0006g0106others(13): Show | 17 | HG02572.hp2 HG02615.hp2 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.876-6055G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112514227 | ||||||
chr2:112514274
|
C | T | 16 | a0001c0002t0006g0012a0001c0002t0006g0104a0001c0002t0006g0106others(13): Show | 17 | HG02572.hp2 HG02615.hp2 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.876-6008C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112514274 | ||||||
chr2:112514326
|
G | C | 1 | a0001c0001t0132g0305 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.876-5956G>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112514326 | ||||||
chr2:112514369
|
A | G | 172 | a0001c0002t0002g0003a0001c0002t0002g0008a0001c0002t0002g0013others(169): Show | 185 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.876-5913A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112514369 | ||||||
chr2:112514381
|
C | CAA | 72 | a0001c0003t0002g0170a0001c0003t0002g0172a0001c0003t0003g0004others(69): Show | 80 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.876-5889_876-5888d others(4): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112514381 | |||||
chr2:112514381
|
CA | C | 7 | a0001c0001t0023g0011a0001c0001t0023g0101a0001c0001t0024g0007others(4): Show | 10 | HG01167.hp2 HG01243.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.876-5888delA | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112514381 | |||||
chr2:112514631
|
T | A | 6 | a0001c0002t0020g0093a0001c0002t0028g0097a0001c0002t0028g0146others(3): Show | 6 | HG01891.hp1 HG02145.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.876-5651T>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112514631 | ||||||
chr2:112514815
|
T | A | 1 | a0001c0002t0052g0236 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.876-5467T>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112514815 | ||||||
chr2:112515045
|
G | A | 6 | a0001c0002t0020g0093a0001c0002t0028g0097a0001c0002t0028g0146others(3): Show | 6 | HG01891.hp1 HG02145.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.876-5237G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112515045 | ||||||
chr2:112515347
|
T | A | 172 | a0001c0002t0002g0003a0001c0002t0002g0008a0001c0002t0002g0013others(169): Show | 185 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.876-4935T>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112515347 | ||||||
chr2:112515392
|
G | C | 1 | a0001c0001t0001g0254 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.876-4890G>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112515392 | ||||||
chr2:112515454
|
AAGT | A | 97 | a0001c0002t0002g0003a0001c0002t0002g0008a0001c0002t0002g0013others(94): Show | 102 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.876-4823_876-4821d others(5): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112515454 | |||||
chr2:112515510
|
T | C | 3 | a0001c0001t0001g0021a0001c0001t0001g0269a0001c0001t0001g0270 | 4 | HG01928.hp1 HG01993.hp1 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.876-4772T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112515510 | ||||||
chr2:112515676
|
G | A | 6 | a0001c0002t0020g0093a0001c0002t0028g0097a0001c0002t0028g0146others(3): Show | 6 | HG01891.hp1 HG02145.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.876-4606G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112515676 | ||||||
chr2:112515803
|
C | T | 1 | a0001c0001t0065g0264 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.876-4479C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112515803 | ||||||
chr2:112515901
|
C | G | 1 | a0001c0002t0042g0088 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.876-4381C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112515901 | ||||||
chr2:112515948
|
G | GAATA | 9 | a0001c0001t0007g0037a0001c0001t0007g0038a0001c0001t0007g0051others(6): Show | 10 | HG00639.hp1 HG01243.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.876-4286_876-4283d others(6): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112515948 | |||||
chr2:112515948
|
G | GAATAAAT others(1): Show |
3 | a0001c0001t0024g0007a0001c0001t0026g0056a0001c0001t0132g0305 | 5 | HG01167.hp2 HG01884.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.876-4290_876-4283d others(10): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112515948 | |||||
chr2:112515948
|
G | GAATAAAT others(5): Show |
1 | a0001c0001t0007g0068 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.876-4294_876-4283d others(14): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112515948 | |||||
chr2:112515948
|
G | GAATAAAT others(9): Show |
3 | a0001c0001t0049g0291a0001c0001t0090g0293a0001c0001t0122g0102 | 3 | HG02723.hp2 NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.876-4298_876-4283d others(18): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112515948 | |||||
chr2:112515948
|
GAATA | G | 19 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0001g0251others(16): Show | 19 | HG01256.hp1 HG01891.hp2 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.876-4286_876-4283d others(6): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112515948 | |||||
chr2:112515948
|
GAATAAAT others(1): Show |
G | 94 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0016others(91): Show | 103 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.876-4290_876-4283d others(10): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112515948 | |||||
chr2:112515948
|
GAATAAAT others(5): Show |
G | 2 | a0001c0001t0032g0193a0001c0001t0089g0206 | 2 | HG02976.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.876-4294_876-4283d others(14): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112515948 | |||||
chr2:112515948
|
GAATAAAT others(9): Show |
G | 1 | a0001c0001t0085g0145 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.876-4298_876-4283d others(18): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112515948 | |||||
chr2:112515948
|
GAATAAAT others(13): Show |
G | 4 | a0001c0001t0025g0009a0001c0001t0025g0042a0001c0002t0127g0039others(1): Show | 5 | HG00738.hp2 HG01256.hp2 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.876-4302_876-4283d others(22): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112515948 | |||||
chr2:112515948
|
GAATAAAT others(17): Show |
G | 174 | a0001c0001t0001g0201a0001c0001t0001g0205a0001c0001t0001g0265others(171): Show | 187 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.876-4306_876-4283d others(26): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112515948 | |||||
chr2:112516042
|
G | A | 1 | a0001c0001t0067g0207 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.876-4240G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112516042 | ||||||
chr2:112516210
|
C | T | 1 | a0001c0001t0001g0271 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.876-4072C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112516210 | ||||||
chr2:112516256
|
A | G | 75 | a0001c0002t0051g0237a0001c0002t0052g0236a0001c0003t0002g0170others(72): Show | 83 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.876-4026A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112516256 | ||||||
chr2:112516314
|
C | A | 1 | a0001c0001t0067g0207 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.876-3968C>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112516314 | ||||||
chr2:112516510
|
C | T | 1 | a0001c0002t0009g0144 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.876-3772C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112516510 | ||||||
chr2:112516535
|
A | G | 2 | a0001c0001t0048g0275a0001c0001t0050g0276 | 2 | HG01346.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.876-3747A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112516535 | ||||||
chr2:112516629
|
G | T | 2 | a0001c0001t0048g0275a0001c0001t0050g0276 | 2 | HG01346.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.876-3653G>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112516629 | ||||||
chr2:112516712
|
C | T | 13 | a0001c0002t0002g0003a0001c0002t0002g0116a0001c0002t0002g0118others(10): Show | 14 | HG00621.hp1 HG00735.hp2 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.876-3570C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112516712 | ||||||
chr2:112516801
|
A | G | 72 | a0001c0002t0002g0003a0001c0002t0002g0008a0001c0002t0002g0013others(69): Show | 76 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.876-3481A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112516801 | ||||||
chr2:112516902
|
A | G | 308 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0016others(305): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.876-3380A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112516902 | ||||||
chr2:112517073
|
C | G | 2 | a0001c0002t0051g0237a0001c0002t0052g0236 | 2 | HG02896.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.876-3209C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112517073 | ||||||
chr2:112517156
|
C | CA | 17 | a0001c0001t0001g0278a0001c0001t0001g0304a0001c0001t0007g0037others(14): Show | 17 | HG00741.hp1 HG01346.hp1 HG01361.hp2 others(14): Show |
intron_variant | MODIFIER | c.876-3103dupA | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112517156 | |||||
chr2:112517156
|
CA | C | 18 | a0001c0001t0005g0217a0001c0001t0007g0054a0001c0001t0087g0190others(15): Show | 18 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(15): Show |
intron_variant | MODIFIER | c.876-3103delA | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112517156 | |||||
chr2:112517156
|
CAA | C | 19 | a0001c0002t0006g0012a0001c0002t0006g0104a0001c0002t0006g0106others(16): Show | 20 | HG00280.hp2 HG01257.hp1 HG01258.hp1 others(17): Show |
intron_variant | MODIFIER | c.876-3104_876-3103d others(4): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112517156 | |||||
chr2:112517156
|
CAAA | C | 53 | a0001c0002t0002g0003a0001c0002t0002g0008a0001c0002t0002g0013others(50): Show | 57 | HG00438.hp1 HG00621.hp1 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.876-3105_876-3103d others(5): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112517156 | |||||
chr2:112517156
|
CAAAAAAA | C | 74 | a0001c0002t0051g0237a0001c0002t0052g0236a0001c0003t0002g0170others(71): Show | 82 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.876-3109_876-3103d others(9): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112517156 | |||||
chr2:112517156
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0026g0056 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.876-3114_876-3103d others(14): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112517156 | |||||
chr2:112517309
|
G | A | 1 | a0001c0002t0142g0095 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.876-2973G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112517309 | ||||||
chr2:112517336
|
C | A | 1 | a0001c0002t0142g0095 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.876-2946C>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112517336 | ||||||
chr2:112517351
|
G | A | 2 | a0001c0001t0046g0195a0001c0001t0047g0141 | 2 | HG02818.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.876-2931G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112517351 | ||||||
chr2:112517438
|
G | A | 2 | a0001c0003t0101g0158a0001c0003t0111g0154 | 2 | HG01975.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.876-2844G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112517438 | ||||||
chr2:112517441
|
GT | G | 9 | a0001c0003t0004g0002a0001c0003t0004g0176a0001c0003t0004g0184others(6): Show | 12 | HG00423.hp2 HG00544.hp2 HG00621.hp2 others(9): Show |
intron_variant | MODIFIER | c.876-2838delT | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112517441 | |||||
chr2:112517540
|
T | G | 1 | a0001c0001t0005g0215 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.876-2742T>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112517540 | ||||||
chr2:112517542
|
T | C | 172 | a0001c0002t0002g0003a0001c0002t0002g0008a0001c0002t0002g0013others(169): Show | 185 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.876-2740T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112517542 | ||||||
chr2:112517543
|
C | G | 1 | a0001c0003t0004g0176 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.876-2739C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112517543 | ||||||
chr2:112517575
|
C | T | 1 | a0001c0003t0003g0164 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.876-2707C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112517575 | ||||||
chr2:112517762
|
A | G | 172 | a0001c0002t0002g0003a0001c0002t0002g0008a0001c0002t0002g0013others(169): Show | 185 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.876-2520A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112517762 | ||||||
chr2:112517953
|
C | CT | 75 | a0001c0002t0051g0237a0001c0002t0052g0236a0001c0003t0002g0170others(72): Show | 83 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.876-2320dupT | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112517953 | |||||
chr2:112518015
|
G | A | 6 | a0001c0002t0020g0093a0001c0002t0028g0097a0001c0002t0028g0146others(3): Show | 6 | HG01891.hp1 HG02145.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.876-2267G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112518015 | ||||||
chr2:112518104
|
G | A | 1 | a0001c0002t0006g0108 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.876-2178G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112518104 | ||||||
chr2:112518135
|
AT | A | 154 | a0001c0001t0007g0052a0001c0002t0002g0003a0001c0002t0002g0008others(151): Show | 166 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.876-2127delT | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112518135 | |||||
chr2:112518142
|
T | C | 13 | a0001c0002t0006g0012a0001c0002t0006g0104a0001c0002t0006g0106others(10): Show | 14 | HG02572.hp2 HG02615.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.876-2140T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112518142 | ||||||
chr2:112518331
|
A | AT | 85 | a0001c0002t0008g0070a0001c0002t0008g0072a0001c0002t0008g0074others(82): Show | 93 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.876-1939dupT | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112518331 | |||||
chr2:112518540
|
C | T | 7 | a0001c0002t0009g0143a0001c0002t0009g0144a0001c0002t0009g0294others(4): Show | 7 | HG01257.hp1 HG01258.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.876-1742C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112518540 | ||||||
chr2:112518678
|
C | CT | 174 | a0001c0001t0001g0270a0001c0001t0014g0030a0001c0001t0014g0031others(171): Show | 187 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.876-1590dupT | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112518678 | |||||
chr2:112518678
|
C | CTT | 8 | a0001c0001t0048g0275a0001c0001t0050g0276a0001c0002t0020g0093others(5): Show | 8 | HG01346.hp1 HG01891.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.876-1591_876-1590d others(4): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112518678 | |||||
chr2:112518800
|
G | A | 1 | a0001c0001t0082g0259 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.876-1482G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112518800 | ||||||
chr2:112518955
|
G | A | 172 | a0001c0002t0002g0003a0001c0002t0002g0008a0001c0002t0002g0013others(169): Show | 185 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.876-1327G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112518955 | ||||||
chr2:112518962
|
A | C | 9 | a0001c0002t0008g0070a0001c0002t0008g0072a0001c0002t0008g0074others(6): Show | 9 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(6): Show |
intron_variant | MODIFIER | c.876-1320A>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112518962 | ||||||
chr2:112518971
|
G | A | 6 | a0001c0002t0020g0093a0001c0002t0028g0097a0001c0002t0028g0146others(3): Show | 6 | HG01891.hp1 HG02145.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.876-1311G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112518971 | ||||||
chr2:112519030
|
C | T | 1 | a0001c0002t0042g0088 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.876-1252C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112519030 | ||||||
chr2:112519053
|
C | G | 17 | a0001c0002t0006g0012a0001c0002t0006g0104a0001c0002t0006g0106others(14): Show | 18 | HG02572.hp2 HG02615.hp2 HG02622.hp1 others(15): Show |
intron_variant | MODIFIER | c.876-1229C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112519053 | ||||||
chr2:112519111
|
G | GGGAAGAT others(318): Show |
1 | a0001c0002t0052g0236 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.876-1160_876-1159i others(327): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112519111 | |||||
chr2:112519139
|
A | G | 172 | a0001c0002t0002g0003a0001c0002t0002g0008a0001c0002t0002g0013others(169): Show | 185 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.876-1143A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112519139 | ||||||
chr2:112519193
|
G | T | 75 | a0001c0002t0051g0237a0001c0002t0052g0236a0001c0003t0002g0170others(72): Show | 83 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.876-1089G>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112519193 | ||||||
chr2:112519245
|
A | G | 1 | a0001c0001t0001g0274 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.876-1037A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112519245 | ||||||
chr2:112519288
|
C | T | 2 | a0001c0001t0001g0263a0001c0001t0001g0273 | 2 | HG02145.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.876-994C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112519288 | ||||||
chr2:112519322
|
T | C | 172 | a0001c0002t0002g0003a0001c0002t0002g0008a0001c0002t0002g0013others(169): Show | 185 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.876-960T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112519322 | ||||||
chr2:112519448
|
C | A | 1 | a0001c0003t0003g0230 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.876-834C>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112519448 | ||||||
chr2:112519493
|
G | T | 172 | a0001c0002t0002g0003a0001c0002t0002g0008a0001c0002t0002g0013others(169): Show | 185 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.876-789G>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112519493 | ||||||
chr2:112519550
|
G | GT | 18 | a0001c0001t0001g0087a0001c0001t0001g0191a0001c0001t0001g0251others(15): Show | 18 | HG00621.hp1 HG01109.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.876-711dupT | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112519550 | |||||
chr2:112519550
|
GT | G | 15 | a0001c0001t0001g0201a0001c0001t0007g0054a0001c0002t0008g0075others(12): Show | 15 | HG00639.hp1 HG01243.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.876-711delT | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112519550 | |||||
chr2:112519550
|
GTT | G | 11 | a0001c0002t0008g0070a0001c0002t0008g0072a0001c0002t0008g0074others(8): Show | 11 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(8): Show |
intron_variant | MODIFIER | c.876-712_876-711del others(2): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112519550 | |||||
chr2:112519550
|
GTTT | G | 95 | a0001c0002t0006g0012a0001c0002t0006g0104a0001c0002t0006g0106others(92): Show | 104 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.876-713_876-711del others(3): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112519550 | |||||
chr2:112519559
|
T | G | 6 | a0001c0002t0020g0093a0001c0002t0028g0097a0001c0002t0028g0146others(3): Show | 6 | HG01891.hp1 HG02145.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.876-723T>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112519559 | ||||||
chr2:112519625
|
A | G | 24 | a0001c0002t0006g0012a0001c0002t0006g0104a0001c0002t0006g0106others(21): Show | 25 | HG01891.hp1 HG02145.hp1 HG02572.hp2 others(22): Show |
intron_variant | MODIFIER | c.876-657A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112519625 | ||||||
chr2:112519640
|
G | A | 75 | a0001c0002t0051g0237a0001c0002t0052g0236a0001c0003t0002g0170others(72): Show | 83 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.876-642G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112519640 | ||||||
chr2:112519759
|
A | G | 1 | a0001c0001t0062g0213 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.876-523A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112519759 | ||||||
chr2:112519859
|
G | C | 172 | a0001c0002t0002g0003a0001c0002t0002g0008a0001c0002t0002g0013others(169): Show | 185 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.876-423G>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112519859 | ||||||
chr2:112519920
|
C | T | 66 | a0001c0002t0002g0003a0001c0002t0002g0008a0001c0002t0002g0013others(63): Show | 70 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.876-362C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112519920 | ||||||
chr2:112519928
|
C | T | 75 | a0001c0002t0051g0237a0001c0002t0052g0236a0001c0003t0002g0170others(72): Show | 83 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.876-354C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112519928 | ||||||
chr2:112519977
|
A | G | 13 | a0001c0002t0006g0012a0001c0002t0006g0104a0001c0002t0006g0106others(10): Show | 14 | HG02572.hp2 HG02615.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.876-305A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112519977 | ||||||
chr2:112520022
|
C | T | 1 | a0001c0001t0026g0056 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.876-260C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112520022 | ||||||
chr2:112520071
|
C | G | 59 | a0001c0001t0001g0017a0001c0001t0001g0197a0001c0001t0001g0201others(56): Show | 63 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.876-211C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112520071 | ||||||
chr2:112520130
|
C | CA | 19 | a0001c0001t0001g0278a0001c0001t0014g0030a0001c0001t0014g0031others(16): Show | 21 | HG01109.hp1 HG01167.hp2 HG01346.hp1 others(18): Show |
intron_variant | MODIFIER | c.876-132dupA | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112520130 | |||||
chr2:112520130
|
CA | C | 97 | a0001c0001t0001g0247a0001c0001t0005g0217a0001c0001t0016g0194others(94): Show | 102 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.876-132delA | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 112520130 | |||||
chr2:112520209
|
T | C | 1 | a0001c0001t0100g0103 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.876-73T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112520209 | ||||||
chr2:112520260
|
C | A | 1 | a0001c0002t0042g0088 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.876-22C>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112520260 | ||||||
chr2:112520273
|
G | T | 1 | a0001c0002t0042g0088 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.876-9G>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 5/6 | chr2 | 112520273 | ||||||
chr2:112520613
|
T | C | 1 | a0001c0001t0132g0305 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1019+188T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112520613 | ||||||
chr2:112520614
|
A | T | 163 | a0001c0001t0076g0090a0001c0001t0085g0145a0001c0001t0132g0305others(160): Show | 176 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.1019+189A>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112520614 | ||||||
chr2:112520615
|
G | GTA | 163 | a0001c0001t0076g0090a0001c0001t0085g0145a0001c0001t0132g0305others(160): Show | 176 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.1019+190_1019+191i others(4): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112520615 | ||||||
chr2:112520616
|
G | A | 163 | a0001c0001t0076g0090a0001c0001t0085g0145a0001c0001t0132g0305others(160): Show | 176 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.1019+191G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112520616 | ||||||
chr2:112520734
|
C | A | 162 | a0001c0002t0002g0003a0001c0002t0002g0008a0001c0002t0002g0013others(159): Show | 175 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.1019+309C>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112520734 | ||||||
chr2:112520778
|
C | T | 2 | a0001c0003t0011g0228a0001c0003t0011g0298 | 2 | NA18948.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.1019+353C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112520778 | ||||||
chr2:112520792
|
C | T | 1 | a0001c0004t0001g0249 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1019+367C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112520792 | ||||||
chr2:112520954
|
G | A | 1 | a0001c0003t0020g0115 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1019+529G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112520954 | ||||||
chr2:112521118
|
G | A | 1 | a0001c0002t0042g0088 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1019+693G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112521118 | ||||||
chr2:112521123
|
C | T | 3 | a0001c0001t0065g0264a0001c0001t0069g0212a0001c0001t0079g0257 | 3 | HG01358.hp2 HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1019+698C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112521123 | ||||||
chr2:112521140
|
G | A | 1 | a0001c0002t0142g0095 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1019+715G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112521140 | ||||||
chr2:112521176
|
G | A | 1 | a0001c0001t0085g0145 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1019+751G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112521176 | ||||||
chr2:112521186
|
G | A | 2 | a0001c0002t0042g0088a0001c0002t0051g0237 | 2 | HG02922.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1019+761G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112521186 | ||||||
chr2:112521287
|
C | T | 1 | a0001c0002t0008g0072 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1019+862C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112521287 | ||||||
chr2:112521410
|
C | G | 1 | a0001c0001t0017g0268 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1019+985C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112521410 | ||||||
chr2:112521415
|
G | A | 1 | a0001c0001t0121g0262 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1019+990G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112521415 | ||||||
chr2:112521534
|
C | G | 1 | a0001c0003t0112g0149 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1019+1109C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112521534 | ||||||
chr2:112521563
|
C | G | 1 | a0001c0001t0120g0100 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1019+1138C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112521563 | ||||||
chr2:112521621
|
C | T | 1 | a0001c0003t0003g0151 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1019+1196C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112521621 | ||||||
chr2:112521737
|
A | G | 2 | a0001c0003t0003g0299a0001c0003t0034g0232 | 2 | HG02129.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.1019+1312A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112521737 | ||||||
chr2:112521857
|
C | T | 1 | a0001c0002t0042g0088 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1019+1432C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112521857 | ||||||
chr2:112521903
|
A | G | 1 | a0001c0002t0042g0088 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1019+1478A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112521903 | ||||||
chr2:112521922
|
C | T | 1 | a0001c0001t0086g0114 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1019+1497C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112521922 | ||||||
chr2:112521937
|
A | C | 288 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0016others(285): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.1019+1512A>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112521937 | ||||||
chr2:112522042
|
T | G | 1 | a0001c0003t0103g0167 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1019+1617T>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112522042 | ||||||
chr2:112522045
|
C | T | 1 | a0001c0002t0002g0119 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1019+1620C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112522045 | ||||||
chr2:112522204
|
G | T | 1 | a0001c0001t0014g0030 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1019+1779G>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112522204 | ||||||
chr2:112522310
|
A | G | 2 | a0001c0002t0053g0233a0001c0002t0054g0234 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1019+1885A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112522310 | ||||||
chr2:112522311
|
T | C | 2 | a0001c0002t0053g0233a0001c0002t0054g0234 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1019+1886T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112522311 | ||||||
chr2:112522420
|
AACCGACA others(2): Show |
A | 3 | a0001c0002t0055g0279a0001c0002t0056g0094a0001c0002t0057g0280 | 3 | HG02145.hp1 HG02647.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1019+1998_1019+200 others(13): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | 112522420 | |||||
chr2:112522676
|
C | G | 9 | a0001c0002t0009g0143a0001c0002t0009g0144a0001c0002t0009g0294others(6): Show | 9 | HG01257.hp1 HG01258.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.1019+2251C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112522676 | ||||||
chr2:112522694
|
A | G | 1 | a0001c0002t0051g0237 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1019+2269A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112522694 | ||||||
chr2:112522776
|
C | T | 1 | a0001c0003t0109g0175 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1019+2351C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112522776 | ||||||
chr2:112523006
|
A | G | 8 | a0001c0002t0002g0008a0001c0002t0002g0122a0001c0002t0002g0131others(5): Show | 10 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.1019+2581A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112523006 | ||||||
chr2:112523032
|
C | T | 2 | a0001c0003t0114g0166a0001c0003t0115g0178 | 2 | NA19003.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1019+2607C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112523032 | ||||||
chr2:112523052
|
C | T | 1 | a0001c0002t0052g0236 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1019+2627C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112523052 | ||||||
chr2:112523176
|
C | G | 1 | a0001c0002t0142g0095 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1019+2751C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112523176 | ||||||
chr2:112523238
|
G | C | 1 | a0001c0001t0001g0304 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1019+2813G>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112523238 | ||||||
chr2:112523303
|
C | T | 130 | a0001c0001t0014g0030a0001c0001t0014g0031a0001c0001t0014g0033others(127): Show | 142 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.1019+2878C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112523303 | ||||||
chr2:112523314
|
C | T | 1 | a0001c0001t0025g0042 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1019+2889C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112523314 | ||||||
chr2:112523332
|
C | T | 273 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0016others(270): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.1019+2907C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112523332 | ||||||
chr2:112523350
|
C | CTG | 7 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0014g0030others(4): Show | 7 | HG02896.hp1 HG02922.hp2 NA18950.hp1 others(4): Show |
intron_variant | MODIFIER | c.1019+2947_1019+294 others(6): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | 112523350 | |||||
chr2:112523350
|
C | CTGTG | 244 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0016others(241): Show | 265 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.1019+2945_1019+294 others(8): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | 112523350 | |||||
chr2:112523350
|
C | CTGTGTG | 25 | a0001c0001t0001g0278a0001c0001t0023g0011a0001c0001t0023g0101others(22): Show | 29 | HG00438.hp1 HG01074.hp1 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.1019+2943_1019+294 others(10): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | 112523350 | |||||
chr2:112523350
|
C | CTGTGTGT others(1): Show |
12 | a0001c0001t0017g0250a0001c0001t0069g0212a0001c0002t0008g0070others(9): Show | 12 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(9): Show |
intron_variant | MODIFIER | c.1019+2941_1019+294 others(12): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | 112523350 | |||||
chr2:112523350
|
C | CTGTGTGT others(3): Show |
14 | a0001c0002t0006g0012a0001c0002t0006g0104a0001c0002t0006g0106others(11): Show | 15 | HG02572.hp2 HG02615.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.1019+2939_1019+294 others(14): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | 112523350 | |||||
chr2:112523350
|
C | CTGTGTGT others(17): Show |
1 | a0001c0002t0042g0088 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1019+2948_1019+294 others(28): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | 112523350 | |||||
chr2:112523469
|
CCTGTCAC others(14): Show |
C | 1 | a0001c0002t0142g0095 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1019+3086_1019+310 others(25): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | 112523469 | |||||
chr2:112523514
|
G | C | 1 | a0001c0001t0079g0257 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1019+3089G>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112523514 | ||||||
chr2:112523546
|
G | A | 3 | a0001c0001t0001g0255a0001c0001t0001g0261a0001c0001t0093g0240 | 3 | HG01257.hp2 HG02738.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1019+3121G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112523546 | ||||||
chr2:112523769
|
A | C | 260 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0016others(257): Show | 285 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.1019+3344A>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112523769 | ||||||
chr2:112523770
|
GT | G | 57 | a0001c0001t0007g0051a0001c0001t0007g0052a0001c0001t0007g0053others(54): Show | 58 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.1019+3356delT | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | 112523770 | |||||
chr2:112523770
|
GTT | G | 259 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0016others(256): Show | 284 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.1019+3355_1019+335 others(6): Show |
TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | 112523770 | |||||
chr2:112524197
|
A | G | 1 | a0001c0001t0001g0247 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1019+3772A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112524197 | ||||||
chr2:112524491
|
C | T | 1 | a0001c0001t0120g0100 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1019+4066C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112524491 | ||||||
chr2:112524579
|
A | G | 8 | a0001c0002t0002g0008a0001c0002t0002g0122a0001c0002t0002g0131others(5): Show | 10 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.1020-4102A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112524579 | ||||||
chr2:112524644
|
A | T | 1 | a0001c0001t0076g0090 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1020-4037A>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112524644 | ||||||
chr2:112524666
|
A | G | 10 | a0001c0002t0008g0070a0001c0002t0008g0072a0001c0002t0008g0074others(7): Show | 10 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1020-4015A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112524666 | ||||||
chr2:112524728
|
C | T | 1 | a0001c0002t0002g0136 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1020-3953C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112524728 | ||||||
chr2:112524923
|
C | T | 15 | a0001c0002t0006g0012a0001c0002t0006g0104a0001c0002t0006g0106others(12): Show | 16 | HG01891.hp1 HG02572.hp2 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.1020-3758C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112524923 | ||||||
chr2:112524924
|
A | G | 308 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0016others(305): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.1020-3757A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112524924 | ||||||
chr2:112524941
|
T | C | 1 | a0001c0002t0057g0280 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1020-3740T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112524941 | ||||||
chr2:112524944
|
A | G | 7 | a0001c0002t0009g0143a0001c0002t0009g0144a0001c0002t0009g0294others(4): Show | 7 | HG01257.hp1 HG01258.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.1020-3737A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112524944 | ||||||
chr2:112525222
|
G | T | 9 | a0001c0002t0008g0070a0001c0002t0008g0072a0001c0002t0008g0074others(6): Show | 9 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1020-3459G>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112525222 | ||||||
chr2:112525271
|
C | T | 130 | a0001c0001t0014g0030a0001c0001t0014g0031a0001c0001t0014g0033others(127): Show | 142 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.1020-3410C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112525271 | ||||||
chr2:112525385
|
A | G | 2 | a0001c0002t0051g0237a0001c0002t0052g0236 | 2 | HG02896.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1020-3296A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112525385 | ||||||
chr2:112525465
|
G | A | 9 | a0001c0001t0007g0051a0001c0001t0007g0052a0001c0001t0007g0053others(6): Show | 9 | HG00639.hp1 HG02717.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.1020-3216G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112525465 | ||||||
chr2:112525474
|
C | T | 10 | a0001c0002t0002g0013a0001c0002t0002g0124a0001c0002t0002g0128others(7): Show | 11 | HG00438.hp1 HG02071.hp2 NA18939.hp1 others(8): Show |
intron_variant | MODIFIER | c.1020-3207C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112525474 | ||||||
chr2:112525514
|
G | A | 8 | a0001c0002t0002g0008a0001c0002t0002g0122a0001c0002t0002g0131others(5): Show | 10 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.1020-3167G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112525514 | ||||||
chr2:112525631
|
A | G | 10 | a0001c0002t0008g0070a0001c0002t0008g0072a0001c0002t0008g0074others(7): Show | 10 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1020-3050A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112525631 | ||||||
chr2:112525726
|
C | T | 1 | a0001c0001t0123g0098 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1020-2955C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112525726 | ||||||
chr2:112525727
|
G | A | 1 | a0001c0001t0088g0086 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1020-2954G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112525727 | ||||||
chr2:112525727
|
G | T | 1 | a0001c0003t0003g0159 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1020-2954G>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112525727 | ||||||
chr2:112525927
|
C | T | 2 | a0001c0001t0024g0007a0001c0001t0122g0102 | 4 | HG01167.hp2 HG02723.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1020-2754C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112525927 | ||||||
chr2:112526024
|
T | A | 1 | a0001c0002t0142g0095 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1020-2657T>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112526024 | ||||||
chr2:112526032
|
TA | T | 15 | a0001c0002t0006g0012a0001c0002t0006g0104a0001c0002t0006g0106others(12): Show | 16 | HG01891.hp1 HG02572.hp2 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.1020-2648delA | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112526032 | ||||||
chr2:112526036
|
G | T | 2 | a0001c0002t0051g0237a0001c0002t0052g0236 | 2 | HG02896.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1020-2645G>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112526036 | ||||||
chr2:112526249
|
T | C | 1 | a0001c0001t0001g0191 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1020-2432T>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112526249 | ||||||
chr2:112526628
|
G | A | 9 | a0001c0002t0008g0070a0001c0002t0008g0072a0001c0002t0008g0074others(6): Show | 9 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1020-2053G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112526628 | ||||||
chr2:112526767
|
T | A | 112 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0016others(109): Show | 122 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.1020-1914T>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112526767 | ||||||
chr2:112526988
|
G | T | 303 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0016others(300): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.1020-1693G>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112526988 | ||||||
chr2:112526999
|
A | G | 2 | a0001c0002t0051g0237a0001c0002t0052g0236 | 2 | HG02896.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1020-1682A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112526999 | ||||||
chr2:112527169
|
C | T | 2 | a0001c0001t0098g0277a0001c0001t0099g0256 | 2 | HG02683.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.1020-1512C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112527169 | ||||||
chr2:112527218
|
G | A | 271 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0016others(268): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.1020-1463G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112527218 | ||||||
chr2:112527219
|
C | A | 271 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0016others(268): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.1020-1462C>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112527219 | ||||||
chr2:112527283
|
G | T | 1 | a0001c0003t0113g0169 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1020-1398G>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112527283 | ||||||
chr2:112527446
|
C | G | 1 | a0001c0001t0085g0145 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1020-1235C>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112527446 | ||||||
chr2:112527468
|
A | G | 1 | a0001c0001t0001g0252 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1020-1213A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112527468 | ||||||
chr2:112527495
|
G | T | 8 | a0001c0001t0007g0051a0001c0001t0007g0052a0001c0001t0007g0053others(5): Show | 8 | HG00639.hp1 HG02717.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1020-1186G>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112527495 | ||||||
chr2:112527499
|
G | T | 9 | a0001c0002t0008g0070a0001c0002t0008g0072a0001c0002t0008g0074others(6): Show | 9 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1020-1182G>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112527499 | ||||||
chr2:112527501
|
A | G | 1 | a0001c0001t0086g0114 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1020-1180A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112527501 | ||||||
chr2:112527676
|
C | T | 1 | a0001c0001t0001g0142 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1020-1005C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112527676 | ||||||
chr2:112528044
|
G | A | 10 | a0001c0002t0008g0070a0001c0002t0008g0072a0001c0002t0008g0074others(7): Show | 10 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1020-637G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112528044 | ||||||
chr2:112528173
|
G | A | 1 | a0001c0002t0002g0138 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1020-508G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112528173 | ||||||
chr2:112528219
|
G | A | 12 | a0001c0002t0009g0143a0001c0002t0009g0144a0001c0002t0009g0294others(9): Show | 12 | HG01243.hp2 HG01257.hp1 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1020-462G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112528219 | ||||||
chr2:112528327
|
C | T | 1 | a0001c0001t0001g0092 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1020-354C>T | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112528327 | ||||||
chr2:112528371
|
G | C | 1 | a0001c0002t0012g0112 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1020-310G>C | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112528371 | ||||||
chr2:112528446
|
A | G | 9 | a0001c0002t0008g0070a0001c0002t0008g0072a0001c0002t0008g0074others(6): Show | 9 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1020-235A>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112528446 | ||||||
chr2:112528468
|
G | A | 1 | a0001c0002t0042g0088 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1020-213G>A | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112528468 | ||||||
chr2:112528618
|
T | G | 1 | a0001c0002t0131g0034 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1020-63T>G | TTL | ENSG00000114999.8 | transcript | ENST00000233336.7 | protein_coding | 6/6 | chr2 | 112528618 |