geneid | 51527 |
---|---|
ensemblid | ENSG00000100744.15 |
hgncid | 20343 |
symbol | GSKIP |
name | GSK3B interacting protein |
refseq_nuc | NM_016472.5 |
refseq_prot | NP_057556.2 |
ensembl_nuc | ENST00000555181.6 |
ensembl_prot | ENSP00000450420.1 |
mane_status | MANE Select |
chr | chr14 |
start | 96363526 |
end | 96387288 |
strand | + |
ver | v1.2 |
region | chr14:96363526-96387288 |
region5000 | chr14:96358526-96392288 |
regionname0 | GSKIP_chr14_96363526_96387288 |
regionname5000 | GSKIP_chr14_96358526_96392288 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 139 | 408 | 94 | 68 | 188 | 14 | 42 | 146 | GSKIP_chr14_96358526_96392288 | GSKIP | copy fasta | chr14 | 96358526 | 96392288 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 420 | 407 | 94 | 68 | 188 | 14 | 41 | GSKIP_chr14_96358526_96392288 | GSKIP | copy fasta | chr14 | 96358526 | 96392288 |
c0002 | 0/0 | 420 | 1 | 0 | 0 | 0 | 0 | 1 | GSKIP_chr14_96358526_96392288 | GSKIP | copy fasta | chr14 | 96358526 | 96392288 |
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 | 1749 | 198 | 68 | 31 | 68 | 5 | 26 | GSKIP_chr14_96358526_96392288 | GSKIP | copy fasta | chr14 | 96358526 | 96392288 |
t0002 | 0/1 | 1749 | 99 | 16 | 24 | 44 | 6 | 8 | GSKIP_chr14_96358526_96392288 | GSKIP | copy fasta | chr14 | 96358526 | 96392288 |
t0003 | 0/0 | 1749 | 89 | 3 | 8 | 67 | 3 | 8 | GSKIP_chr14_96358526_96392288 | GSKIP | copy fasta | chr14 | 96358526 | 96392288 |
t0004 | 1/0 | 1749 | 7 | 0 | 2 | 4 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | copy fasta | chr14 | 96358526 | 96392288 |
t0005 | 0/0 | 1749 | 4 | 3 | 1 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | copy fasta | chr14 | 96358526 | 96392288 |
t0006 | 0/0 | 1749 | 3 | 3 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | copy fasta | chr14 | 96358526 | 96392288 |
t0007 | 0/0 | 1728 | 1 | 0 | 1 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | copy fasta | chr14 | 96358526 | 96392288 |
t0008 | 0/0 | 1749 | 1 | 0 | 1 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | copy fasta | chr14 | 96358526 | 96392288 |
t0009 | 0/0 | 1749 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | copy fasta | chr14 | 96358526 | 96392288 |
t0010 | 0/0 | 1749 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | copy fasta | chr14 | 96358526 | 96392288 |
t0011 | 0/0 | 1749 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | copy fasta | chr14 | 96358526 | 96392288 |
t0012 | 0/0 | 1749 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | copy fasta | chr14 | 96358526 | 96392288 |
t0013 | 0/0 | 1749 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | copy fasta | chr14 | 96358526 | 96392288 |
t0014 | 0/0 | 1749 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | copy fasta | chr14 | 96358526 | 96392288 |
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 | 52 | 2 | 5 | 40 | 2 | 3 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0002 | 0/0 | 43 | 1 | 8 | 25 | 3 | 6 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0003 | 0/0 | 40 | 9 | 7 | 16 | 4 | 4 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0004 | 0/0 | 32 | 1 | 6 | 19 | 1 | 5 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0005 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0006 | 0/0 | 6 | 1 | 5 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0007 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0008 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0009 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0010 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0011 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0012 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0014 | 1/0 | 4 | 0 | 0 | 3 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0016 | 0/0 | 3 | 2 | 0 | 0 | 0 | 1 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0017 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0021 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0022 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0026 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0027 | 0/1 | 2 | 0 | 0 | 0 | 1 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0037 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0040 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0042 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 420 | 407 | 94 | 68 | 188 | 14 | 41 | GSKIP_chr14_96358526_96392288 | GSKIP | copy fasta | chr14 | 96358526 | 96392288 |
a0001c0002 | 0/0 | 420 | 1 | 0 | 0 | 0 | 0 | 1 | GSKIP_chr14_96358526_96392288 | GSKIP | copy fasta | chr14 | 96358526 | 96392288 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2168 | 197 | 68 | 31 | 68 | 5 | 25 | GSKIP_chr14_96358526_96392288 | GSKIP | copy fasta | chr14 | 96358526 | 96392288 |
a0001c0001t0002 | 0/1 | 2168 | 99 | 16 | 24 | 44 | 6 | 8 | GSKIP_chr14_96358526_96392288 | GSKIP | copy fasta | chr14 | 96358526 | 96392288 |
a0001c0001t0003 | 0/0 | 2168 | 89 | 3 | 8 | 67 | 3 | 8 | GSKIP_chr14_96358526_96392288 | GSKIP | copy fasta | chr14 | 96358526 | 96392288 |
a0001c0001t0004 | 1/0 | 2168 | 7 | 0 | 2 | 4 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | copy fasta | chr14 | 96358526 | 96392288 |
a0001c0001t0005 | 0/0 | 2168 | 4 | 3 | 1 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | copy fasta | chr14 | 96358526 | 96392288 |
a0001c0001t0006 | 0/0 | 2168 | 3 | 3 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | copy fasta | chr14 | 96358526 | 96392288 |
a0001c0001t0007 | 0/0 | 2147 | 1 | 0 | 1 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | copy fasta | chr14 | 96358526 | 96392288 |
a0001c0001t0008 | 0/0 | 2168 | 1 | 0 | 1 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | copy fasta | chr14 | 96358526 | 96392288 |
a0001c0001t0009 | 0/0 | 2168 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | copy fasta | chr14 | 96358526 | 96392288 |
a0001c0001t0010 | 0/0 | 2168 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | copy fasta | chr14 | 96358526 | 96392288 |
a0001c0001t0011 | 0/0 | 2168 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | copy fasta | chr14 | 96358526 | 96392288 |
a0001c0001t0012 | 0/0 | 2168 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | copy fasta | chr14 | 96358526 | 96392288 |
a0001c0001t0013 | 0/0 | 2168 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | copy fasta | chr14 | 96358526 | 96392288 |
a0001c0001t0014 | 0/0 | 2168 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | copy fasta | chr14 | 96358526 | 96392288 |
a0001c0002t0001 | 0/0 | 2168 | 1 | 0 | 0 | 0 | 0 | 1 | GSKIP_chr14_96358526_96392288 | GSKIP | copy fasta | chr14 | 96358526 | 96392288 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 40 | 9 | 7 | 16 | 4 | 4 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0004 | 0/0 | 30 | 1 | 6 | 18 | 1 | 4 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0005 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0007 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0009 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0012 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0016 | 0/0 | 3 | 2 | 0 | 0 | 0 | 1 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0002g0002 | 0/0 | 43 | 1 | 8 | 25 | 3 | 6 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0002g0006 | 0/0 | 6 | 1 | 5 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0002g0008 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0002g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0002g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0002g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0002g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0002g0026 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0002g0027 | 0/1 | 2 | 0 | 0 | 0 | 1 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0003g0001 | 0/0 | 49 | 2 | 4 | 38 | 2 | 3 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0003g0010 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0003g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0003g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0003g0021 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0003g0022 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0003g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0003g0042 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0003g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0003g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0003g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0003g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0004g0001 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0004g0014 | 1/0 | 3 | 0 | 0 | 2 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0004g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0004g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0005g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0005g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0005g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0006g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0006g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0007g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0008g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0009g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0010g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0011g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0012g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0013g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0001t0014g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
a0001c0002t0001g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0055 | EUR | GBR | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | GBR | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0065 | EUR | FIN | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | FIN | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG00323 | hp2 | a0001 | c0001 | t0003 | g0001 | EUR | FIN | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG00408 | hp2 | a0001 | c0001 | t0003 | g0152 | EAS | CHS | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | CHS | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG00438 | hp2 | a0001 | c0001 | t0003 | g0020 | EAS | CHS | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG00544 | hp1 | a0001 | c0001 | t0004 | g0014 | EAS | CHS | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG00544 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | CHS | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG00558 | hp1 | a0001 | c0001 | t0003 | g0162 | EAS | CHS | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG00597 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | CHS | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG00642 | hp1 | a0001 | c0001 | t0005 | g0106 | AMR | PUR | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG00673 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | CHS | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG00735 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0074 | AMR | PUR | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0059 | AMR | PUR | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG01070 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG01074 | hp1 | a0001 | c0001 | t0003 | g0021 | AMR | PUR | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0070 | AMR | PUR | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG01081 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0136 | AMR | PUR | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG01192 | hp1 | a0001 | c0001 | t0003 | g0153 | AMR | PUR | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | CLM | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | CLM | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG01256 | hp2 | a0001 | c0001 | t0004 | g0021 | AMR | CLM | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | CLM | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG01258 | hp1 | a0001 | c0001 | t0004 | g0001 | AMR | CLM | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | CLM | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG01346 | hp2 | a0001 | c0001 | t0008 | g0011 | AMR | CLM | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | CLM | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | CLM | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | IBS | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG01515 | hp2 | a0001 | c0001 | t0003 | g0001 | EUR | IBS | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG01891 | hp1 | a0001 | c0001 | t0005 | g0107 | AFR | ACB | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG01928 | hp1 | a0001 | c0001 | t0003 | g0151 | AMR | PEL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0051 | AMR | PEL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PEL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG01952 | hp2 | a0001 | c0001 | t0003 | g0022 | AMR | PEL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0064 | AMR | PEL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02015 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02027 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0066 | AFR | ACB | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | ACB | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02056 | hp1 | a0001 | c0001 | t0003 | g0161 | EAS | KHV | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02074 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | KHV | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | KHV | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02080 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02083 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | KHV | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0047 | AFR | ACB | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0071 | AMR | PEL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CDX | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02155 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | CDX | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02165 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | CDX | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | CDX | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0061 | AFR | ACB | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | ACB | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0075 | AFR | ACB | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02293 | hp2 | a0001 | c0001 | t0007 | g0011 | AMR | PEL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0026 | AMR | PEL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02451 | hp2 | a0001 | c0001 | t0003 | g0001 | AFR | ACB | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0023 | AFR | GWD | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02647 | hp2 | a0001 | c0001 | t0002 | g0025 | AFR | GWD | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02683 | hp2 | a0001 | c0001 | t0003 | g0001 | SAS | PJL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0024 | AFR | GWD | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02723 | hp1 | a0001 | c0001 | t0002 | g0024 | AFR | GWD | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02809 | hp2 | a0001 | c0001 | t0005 | g0035 | AFR | GWD | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02922 | hp1 | a0001 | c0001 | t0006 | g0164 | AFR | ESN | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0048 | AFR | ESN | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | ESN | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | ESN | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | ESN | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | ESN | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG03017 | hp2 | a0001 | c0001 | t0003 | g0149 | SAS | PJL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG03041 | hp1 | a0001 | c0001 | t0003 | g0156 | AFR | GWD | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG03130 | hp1 | a0001 | c0001 | t0005 | g0035 | AFR | ESN | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG03139 | hp1 | a0001 | c0001 | t0006 | g0045 | AFR | ESN | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG03139 | hp2 | a0001 | c0001 | t0009 | g0009 | AFR | ESN | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | ESN | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | ESN | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | MSL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0122 | SAS | PJL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | MSL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG03490 | hp1 | a0001 | c0001 | t0003 | g0001 | SAS | PJL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG03491 | hp1 | a0001 | c0001 | t0003 | g0042 | SAS | PJL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG03492 | hp2 | a0001 | c0001 | t0003 | g0042 | SAS | PJL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG03516 | hp2 | a0001 | c0001 | t0006 | g0045 | AFR | ESN | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | MSL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG03669 | hp1 | a0001 | c0001 | t0003 | g0022 | SAS | PJL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | STU | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | STU | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG03710 | hp1 | a0001 | c0001 | t0003 | g0010 | SAS | PJL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG03831 | hp1 | a0001 | c0002 | t0001 | g0004 | SAS | BEB | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | BEB | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | BEB | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | BEB | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | BEB | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | BEB | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0057 | SAS | BEB | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | STU | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | STU | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | BEB | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | BEB | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | STU | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | STU | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | YRI | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18522 | hp2 | a0001 | c0001 | t0003 | g0001 | AFR | YRI | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18612 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | CHB | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | CHB | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHB | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHB | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | YRI | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0025 | AFR | YRI | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18939 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18940 | hp2 | a0001 | c0001 | t0003 | g0044 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18942 | hp1 | a0001 | c0001 | t0003 | g0155 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18943 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18945 | hp2 | a0001 | c0001 | t0014 | g0001 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18946 | hp2 | a0001 | c0001 | t0003 | g0147 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18948 | hp1 | a0001 | c0001 | t0003 | g0109 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18950 | hp1 | a0001 | c0001 | t0003 | g0145 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18952 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18954 | hp2 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18956 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18959 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18960 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18961 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18965 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18968 | hp2 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18973 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18973 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18975 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18977 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18977 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18978 | hp2 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18980 | hp2 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18984 | hp2 | a0001 | c0001 | t0004 | g0146 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18985 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18987 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18989 | hp1 | a0001 | c0001 | t0003 | g0154 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18990 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18991 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18993 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18994 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18998 | hp2 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA19001 | hp1 | a0001 | c0001 | t0003 | g0108 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA19001 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA19005 | hp2 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA19007 | hp2 | a0001 | c0001 | t0010 | g0004 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA19011 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA19012 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA19012 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | LWK | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | LWK | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | LWK | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | LWK | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA19054 | hp2 | a0001 | c0001 | t0003 | g0157 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA19055 | hp1 | a0001 | c0001 | t0003 | g0150 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA19056 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA19060 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA19062 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA19062 | hp2 | a0001 | c0001 | t0012 | g0144 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA19064 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA19068 | hp1 | a0001 | c0001 | t0003 | g0158 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA19068 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA19070 | hp1 | a0001 | c0001 | t0011 | g0005 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA19070 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA19072 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA19072 | hp2 | a0001 | c0001 | t0013 | g0160 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA19077 | hp1 | a0001 | c0001 | t0003 | g0148 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA19077 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA19079 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA19080 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA19081 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA19082 | hp1 | a0001 | c0001 | t0004 | g0014 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA19082 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA19084 | hp1 | a0001 | c0001 | t0003 | g0044 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA19085 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA19086 | hp2 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA19088 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA19089 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA19090 | hp2 | a0001 | c0001 | t0003 | g0110 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0049 | AFR | YRI | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | YRI | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ASW | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | ASW | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA20805 | hp1 | a0001 | c0001 | t0003 | g0021 | EUR | TSI | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0027 | EUR | TSI | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | GIH | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA20905 | hp2 | a0001 | c0001 | t0003 | g0001 | SAS | GIH | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG01123 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | CLM | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0053 | AFR | ACB | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | ACB | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0046 | AFR | ACB | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | MSL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | MSL | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | USA | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | USA | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | USA | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | USA | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0023 | AFR | LWK | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | LWK | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0027 | REF | REF | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0004 | g0014 | REF | REF | GSKIP_chr14_96358526_96392288 | GSKIP | chr14 | 96358526 | 96392288 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:96382298
|
A | G | 1 | a0001c0002 | 1 | HG03831.hp1 | synonymous_variant | LOW | c.51A>G | p.Glu17Glu | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 3/4 | 196/2169 | 51/420 | 17/139 | chr14 | 96382298 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:96363551
|
A | G | 1 | a0001c0001t0014 | 1 | NA18945.hp2 | 5_prime_UTR_variant | MODIFIER | c.-120A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/4 | 18697 | chr14 | 96363551 | |||||
chr14:96379755
|
G | A | 10 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(7): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
5_prime_UTR_variant | MODIFIER | c.-35G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 2/4 | 2493 | chr14 | 96379755 | |||||
chr14:96385734
|
T | C | 3 | a0001c0001t0002a0001c0001t0007a0001c0001t0008 | 101 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*50T>C | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 4/4 | 50 | chr14 | 96385734 | |||||
chr14:96385887
|
C | G | 1 | a0001c0001t0011 | 1 | NA19070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*203C>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 4/4 | 203 | chr14 | 96385887 | |||||
chr14:96386154
|
A | G | 1 | a0001c0001t0006 | 3 | HG02922.hp1 HG03139.hp1 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*470A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 4/4 | 470 | chr14 | 96386154 | |||||
chr14:96386496
|
CTGTGTTG others(14): Show |
C | 1 | a0001c0001t0007 | 1 | HG02293.hp2 | 3_prime_UTR_variant | MODIFIER | c.*818_*838delTGATTC others(15): Show |
GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 4/4 | 818 | INFO_REALIGN_3_PRIME | chr14 | 96386496 | ||||
chr14:96386576
|
T | A | 1 | a0001c0001t0009 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*892T>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 4/4 | 892 | chr14 | 96386576 | |||||
chr14:96386587
|
T | C | 1 | a0001c0001t0007 | 1 | HG02293.hp2 | 3_prime_UTR_variant | MODIFIER | c.*903T>C | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 4/4 | 903 | chr14 | 96386587 | |||||
chr14:96386594
|
T | C | 1 | a0001c0001t0012 | 1 | NA19062.hp2 | 3_prime_UTR_variant | MODIFIER | c.*910T>C | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 4/4 | 910 | chr14 | 96386594 | |||||
chr14:96386745
|
T | C | 1 | a0001c0001t0010 | 1 | NA19007.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1061T>C | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 4/4 | 1061 | chr14 | 96386745 | |||||
chr14:96386957
|
A | C | 1 | a0001c0001t0008 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1273A>C | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 4/4 | 1273 | chr14 | 96386957 | |||||
chr14:96386993
|
C | T | 1 | a0001c0001t0005 | 4 | HG00642.hp1 HG01891.hp1 HG02809.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1309C>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 4/4 | 1309 | chr14 | 96386993 | |||||
chr14:96387117
|
C | T | 14 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(11): Show | 401 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(398): Show |
3_prime_UTR_variant | MODIFIER | c.*1433C>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 4/4 | 1433 | chr14 | 96387117 | |||||
chr14:96387198
|
T | G | 1 | a0001c0001t0013 | 1 | NA19072.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1514T>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 4/4 | 1514 | chr14 | 96387198 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:96363661
|
G | A | 42 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0008others(39): Show | 99 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.-103+93G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96363661 | ||||||
chr14:96363696
|
G | A | 1 | a0001c0001t0001g0077 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-103+128G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96363696 | ||||||
chr14:96363748
|
C | A | 1 | a0001c0001t0001g0078 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-103+180C>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96363748 | ||||||
chr14:96363771
|
C | T | 4 | a0001c0001t0001g0078a0001c0001t0001g0163a0001c0001t0006g0045others(1): Show | 5 | HG02486.hp2 HG02922.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-103+203C>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96363771 | ||||||
chr14:96363990
|
T | G | 2 | a0001c0001t0001g0015a0001c0001t0001g0079 | 4 | HG02886.hp2 HG03486.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.-103+422T>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96363990 | ||||||
chr14:96364089
|
G | C | 42 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0015others(39): Show | 98 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.-103+521G>C | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96364089 | ||||||
chr14:96364104
|
G | A | 2 | a0001c0001t0002g0023a0001c0001t0002g0046 | 3 | HG02559.hp1 HG02572.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-103+536G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96364104 | ||||||
chr14:96364147
|
A | G | 1 | a0001c0001t0005g0107 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-103+579A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96364147 | ||||||
chr14:96364197
|
G | A | 4 | a0001c0001t0003g0036a0001c0001t0003g0108a0001c0001t0003g0109others(1): Show | 5 | NA18948.hp1 NA18968.hp2 NA18980.hp2 others(2): Show |
intron_variant | MODIFIER | c.-103+629G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96364197 | ||||||
chr14:96364378
|
T | G | 1 | a0001c0001t0001g0111 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-103+810T>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96364378 | ||||||
chr14:96364508
|
G | A | 1 | a0001c0001t0001g0028 | 2 | HG02698.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.-103+940G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96364508 | ||||||
chr14:96364646
|
C | T | 3 | a0001c0001t0005g0035a0001c0001t0005g0106a0001c0001t0005g0107 | 4 | HG00642.hp1 HG01891.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.-103+1078C>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96364646 | ||||||
chr14:96364666
|
C | A | 1 | a0001c0001t0001g0080 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-103+1098C>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96364666 | ||||||
chr14:96364794
|
G | A | 8 | a0001c0001t0001g0018a0001c0001t0001g0037a0001c0001t0001g0038others(5): Show | 12 | HG00621.hp2 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.-103+1226G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96364794 | ||||||
chr14:96364855
|
G | A | 1 | a0001c0001t0005g0106 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-103+1287G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96364855 | ||||||
chr14:96364855
|
G | C | 2 | a0001c0001t0001g0007a0001c0001t0001g0117 | 7 | HG00642.hp2 HG02109.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.-103+1287G>C | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96364855 | ||||||
chr14:96365028
|
A | G | 1 | a0001c0001t0003g0162 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-103+1460A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96365028 | ||||||
chr14:96365125
|
C | T | 2 | a0001c0001t0001g0007a0001c0001t0001g0117 | 7 | HG00642.hp2 HG02109.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.-103+1557C>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96365125 | ||||||
chr14:96365277
|
T | G | 8 | a0001c0001t0001g0018a0001c0001t0001g0037a0001c0001t0001g0038others(5): Show | 12 | HG00621.hp2 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.-103+1709T>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96365277 | ||||||
chr14:96365584
|
CT | C | 135 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(132): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.-103+2020delT | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr14 | 96365584 | |||||
chr14:96365606
|
G | A | 7 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0118others(4): Show | 12 | HG02145.hp1 HG02717.hp2 HG02895.hp1 others(9): Show |
intron_variant | MODIFIER | c.-103+2038G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96365606 | ||||||
chr14:96365613
|
T | G | 2 | a0001c0001t0001g0012a0001c0001t0001g0081 | 5 | HG01192.hp2 HG01257.hp2 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.-103+2045T>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96365613 | ||||||
chr14:96365793
|
C | T | 5 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0117others(2): Show | 13 | HG00642.hp2 HG01255.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.-103+2225C>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96365793 | ||||||
chr14:96365848
|
A | G | 1 | a0001c0001t0001g0116 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-103+2280A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96365848 | ||||||
chr14:96366050
|
G | A | 1 | a0001c0001t0003g0108 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-103+2482G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96366050 | ||||||
chr14:96366107
|
CAT | C | 4 | a0001c0001t0001g0017a0001c0001t0001g0104a0001c0001t0001g0139others(1): Show | 6 | HG03927.hp1 NA18941.hp1 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.-103+2540_-103+254 others(6): Show |
GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96366107 | ||||||
chr14:96366119
|
T | C | 1 | a0001c0001t0001g0082 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-103+2551T>C | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96366119 | ||||||
chr14:96366365
|
G | A | 3 | a0001c0001t0002g0047a0001c0001t0002g0048a0001c0001t0002g0049 | 3 | HG02145.hp2 HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-103+2797G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96366365 | ||||||
chr14:96366482
|
C | G | 1 | a0001c0001t0001g0103 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-103+2914C>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96366482 | ||||||
chr14:96366659
|
A | G | 8 | a0001c0001t0001g0018a0001c0001t0001g0037a0001c0001t0001g0038others(5): Show | 12 | HG00621.hp2 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.-103+3091A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96366659 | ||||||
chr14:96366665
|
G | A | 22 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0039others(19): Show | 60 | HG00099.hp1 HG00408.hp1 HG01099.hp1 others(57): Show |
intron_variant | MODIFIER | c.-103+3097G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96366665 | ||||||
chr14:96366746
|
TTA | T | 4 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0112others(1): Show | 6 | HG02735.hp2 HG03239.hp1 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.-103+3179_-103+318 others(6): Show |
GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96366746 | ||||||
chr14:96366752
|
AAG | A | 3 | a0001c0001t0001g0018a0001c0001t0001g0113a0001c0001t0001g0114 | 5 | HG00621.hp2 HG02040.hp1 HG02523.hp2 others(2): Show |
intron_variant | MODIFIER | c.-103+3186_-103+318 others(6): Show |
GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr14 | 96366752 | |||||
chr14:96366754
|
G | A | 4 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0112others(1): Show | 6 | HG02735.hp2 HG03239.hp1 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.-103+3186G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96366754 | ||||||
chr14:96366849
|
G | A | 1 | a0001c0001t0002g0050 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-103+3281G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96366849 | ||||||
chr14:96366890
|
T | C | 2 | a0001c0001t0001g0078a0001c0001t0001g0163 | 2 | HG02486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-103+3322T>C | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96366890 | ||||||
chr14:96367086
|
C | T | 4 | a0001c0001t0001g0078a0001c0001t0001g0163a0001c0001t0006g0045others(1): Show | 5 | HG02486.hp2 HG02922.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-103+3518C>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96367086 | ||||||
chr14:96367257
|
G | A | 8 | a0001c0001t0001g0018a0001c0001t0001g0037a0001c0001t0001g0038others(5): Show | 12 | HG00621.hp2 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.-103+3689G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96367257 | ||||||
chr14:96367641
|
C | T | 7 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0118others(4): Show | 12 | HG02145.hp1 HG02717.hp2 HG02895.hp1 others(9): Show |
intron_variant | MODIFIER | c.-103+4073C>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96367641 | ||||||
chr14:96367908
|
G | C | 7 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0118others(4): Show | 12 | HG02145.hp1 HG02717.hp2 HG02895.hp1 others(9): Show |
intron_variant | MODIFIER | c.-103+4340G>C | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96367908 | ||||||
chr14:96367914
|
G | C | 1 | a0001c0001t0002g0122 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-103+4346G>C | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96367914 | ||||||
chr14:96368012
|
T | C | 1 | a0001c0001t0001g0083 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-103+4444T>C | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96368012 | ||||||
chr14:96368060
|
A | G | 1 | a0001c0001t0002g0075 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-103+4492A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96368060 | ||||||
chr14:96368082
|
A | AT | 9 | a0001c0001t0001g0018a0001c0001t0001g0037a0001c0001t0001g0038others(6): Show | 13 | HG00621.hp2 HG02040.hp1 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.-103+4529dupT | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr14 | 96368082 | |||||
chr14:96368097
|
T | C | 1 | a0001c0001t0012g0144 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-103+4529T>C | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96368097 | ||||||
chr14:96368184
|
C | CT | 38 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(35): Show | 86 | HG00099.hp1 HG00408.hp1 HG00642.hp1 others(83): Show |
intron_variant | MODIFIER | c.-103+4632dupT | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr14 | 96368184 | |||||
chr14:96368250
|
G | A | 2 | a0001c0001t0006g0045a0001c0001t0006g0164 | 3 | HG02922.hp1 HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-103+4682G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96368250 | ||||||
chr14:96368301
|
C | G | 2 | a0001c0001t0001g0120a0001c0001t0001g0121 | 2 | HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-103+4733C>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96368301 | ||||||
chr14:96368332
|
C | T | 1 | a0001c0001t0013g0160 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.-103+4764C>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96368332 | ||||||
chr14:96368343
|
A | AT | 6 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0119others(3): Show | 11 | HG02145.hp1 HG02717.hp2 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.-103+4782dupT | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr14 | 96368343 | |||||
chr14:96368454
|
G | A | 1 | a0001c0001t0002g0047 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-103+4886G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96368454 | ||||||
chr14:96368470
|
A | T | 1 | a0001c0001t0001g0102 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-103+4902A>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96368470 | ||||||
chr14:96368507
|
T | C | 1 | a0001c0001t0003g0145 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-103+4939T>C | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96368507 | ||||||
chr14:96369127
|
G | A | 1 | a0001c0001t0003g0020 | 3 | HG00438.hp2 NA19005.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.-103+5559G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96369127 | ||||||
chr14:96369204
|
C | T | 4 | a0001c0001t0001g0078a0001c0001t0001g0163a0001c0001t0006g0045others(1): Show | 5 | HG02486.hp2 HG02922.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-103+5636C>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96369204 | ||||||
chr14:96369251
|
T | C | 1 | a0001c0001t0001g0123 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-103+5683T>C | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96369251 | ||||||
chr14:96369615
|
C | T | 2 | a0001c0001t0003g0157a0001c0001t0003g0158 | 2 | NA19054.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.-103+6047C>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96369615 | ||||||
chr14:96369647
|
A | G | 1 | a0001c0001t0003g0156 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-103+6079A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96369647 | ||||||
chr14:96369651
|
G | A | 8 | a0001c0001t0001g0018a0001c0001t0001g0037a0001c0001t0001g0038others(5): Show | 12 | HG00621.hp2 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.-103+6083G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96369651 | ||||||
chr14:96369801
|
A | G | 4 | a0001c0001t0001g0078a0001c0001t0001g0163a0001c0001t0006g0045others(1): Show | 5 | HG02486.hp2 HG02922.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-103+6233A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96369801 | ||||||
chr14:96369956
|
A | G | 1 | a0001c0001t0001g0159 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-103+6388A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96369956 | ||||||
chr14:96370181
|
G | A | 1 | a0001c0001t0001g0124 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-103+6613G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96370181 | ||||||
chr14:96370227
|
A | G | 44 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0015others(41): Show | 99 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(96): Show |
intron_variant | MODIFIER | c.-103+6659A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96370227 | ||||||
chr14:96370458
|
G | A | 3 | a0001c0001t0005g0035a0001c0001t0005g0106a0001c0001t0005g0107 | 4 | HG00642.hp1 HG01891.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.-103+6890G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96370458 | ||||||
chr14:96370551
|
C | T | 5 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0117others(2): Show | 13 | HG00642.hp2 HG01255.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.-103+6983C>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96370551 | ||||||
chr14:96370552
|
G | A | 3 | a0001c0001t0001g0029a0001c0001t0001g0084a0001c0001t0001g0085 | 4 | HG02572.hp2 HG02622.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-103+6984G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96370552 | ||||||
chr14:96370587
|
C | G | 42 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0008others(39): Show | 98 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.-103+7019C>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96370587 | ||||||
chr14:96370636
|
T | C | 138 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(135): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.-103+7068T>C | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96370636 | ||||||
chr14:96370727
|
G | A | 1 | a0001c0001t0002g0051 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-103+7159G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96370727 | ||||||
chr14:96370860
|
G | C | 4 | a0001c0001t0001g0078a0001c0001t0001g0163a0001c0001t0006g0045others(1): Show | 5 | HG02486.hp2 HG02922.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-103+7292G>C | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96370860 | ||||||
chr14:96370904
|
A | T | 8 | a0001c0001t0001g0018a0001c0001t0001g0037a0001c0001t0001g0038others(5): Show | 12 | HG00621.hp2 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.-103+7336A>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96370904 | ||||||
chr14:96370944
|
G | C | 8 | a0001c0001t0001g0018a0001c0001t0001g0037a0001c0001t0001g0038others(5): Show | 12 | HG00621.hp2 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.-103+7376G>C | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96370944 | ||||||
chr14:96371052
|
T | C | 47 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0015others(44): Show | 103 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(100): Show |
intron_variant | MODIFIER | c.-103+7484T>C | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96371052 | ||||||
chr14:96371371
|
A | G | 3 | a0001c0001t0001g0018a0001c0001t0001g0113a0001c0001t0001g0114 | 5 | HG00621.hp2 HG02040.hp1 HG02523.hp2 others(2): Show |
intron_variant | MODIFIER | c.-103+7803A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96371371 | ||||||
chr14:96371442
|
C | CT | 6 | a0001c0001t0001g0040a0001c0001t0002g0027a0001c0001t0003g0022others(3): Show | 11 | HG01952.hp2 HG02056.hp1 HG03669.hp1 others(8): Show |
intron_variant | MODIFIER | c.-103+7894dupT | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr14 | 96371442 | |||||
chr14:96371442
|
CT | C | 71 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(68): Show | 143 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.-103+7894delT | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr14 | 96371442 | |||||
chr14:96371442
|
CTT | C | 40 | a0001c0001t0001g0018a0001c0001t0001g0037a0001c0001t0001g0038others(37): Show | 94 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.-103+7893_-103+789 others(6): Show |
GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr14 | 96371442 | |||||
chr14:96371460
|
T | C | 7 | a0001c0001t0001g0018a0001c0001t0001g0037a0001c0001t0001g0038others(4): Show | 11 | HG00621.hp2 HG02040.hp1 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.-103+7892T>C | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96371460 | ||||||
chr14:96371470
|
AGTCTCAC others(3): Show |
A | 1 | a0001c0001t0001g0030 | 2 | HG01261.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.-103+7906_-103+791 others(14): Show |
GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr14 | 96371470 | |||||
chr14:96371540
|
G | T | 1 | a0001c0001t0002g0065 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-103+7972G>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96371540 | ||||||
chr14:96371591
|
C | T | 1 | a0001c0001t0001g0159 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-103+8023C>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96371591 | ||||||
chr14:96371647
|
A | G | 6 | a0001c0001t0002g0011a0001c0001t0002g0050a0001c0001t0002g0051others(3): Show | 7 | HG01346.hp2 HG01433.hp1 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.-102-8041A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96371647 | ||||||
chr14:96371665
|
A | G | 171 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(168): Show | 403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
intron_variant | MODIFIER | c.-102-8023A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96371665 | ||||||
chr14:96372024
|
G | A | 3 | a0001c0001t0001g0039a0001c0001t0001g0126a0001c0001t0001g0127 | 4 | HG01168.hp2 HG01169.hp1 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.-102-7664G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96372024 | ||||||
chr14:96372456
|
C | G | 1 | a0001c0001t0002g0049 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-102-7232C>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96372456 | ||||||
chr14:96372510
|
G | T | 3 | a0001c0001t0001g0013a0001c0001t0001g0141a0001c0001t0001g0142 | 6 | HG01255.hp2 HG02559.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-102-7178G>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96372510 | ||||||
chr14:96372569
|
T | G | 8 | a0001c0001t0001g0018a0001c0001t0001g0037a0001c0001t0001g0038others(5): Show | 12 | HG00621.hp2 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.-102-7119T>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96372569 | ||||||
chr14:96372675
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-102-7013G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96372675 | ||||||
chr14:96372849
|
G | A | 8 | a0001c0001t0001g0018a0001c0001t0001g0037a0001c0001t0001g0038others(5): Show | 12 | HG00621.hp2 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.-102-6839G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96372849 | ||||||
chr14:96372853
|
A | G | 2 | a0001c0001t0002g0025a0001c0001t0002g0075 | 3 | HG02280.hp2 HG02647.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-102-6835A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96372853 | ||||||
chr14:96373094
|
G | A | 24 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0039others(21): Show | 63 | HG00099.hp1 HG00408.hp1 HG01099.hp1 others(60): Show |
intron_variant | MODIFIER | c.-102-6594G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96373094 | ||||||
chr14:96373193
|
A | G | 1 | a0001c0001t0001g0100 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-102-6495A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96373193 | ||||||
chr14:96373229
|
C | CA | 43 | a0001c0001t0001g0041a0001c0001t0001g0087a0001c0001t0001g0135others(40): Show | 100 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.-102-6436dupA | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr14 | 96373229 | |||||
chr14:96373229
|
C | CAA | 7 | a0001c0001t0002g0008a0001c0001t0002g0026a0001c0001t0002g0052others(4): Show | 12 | HG00438.hp1 HG01256.hp1 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.-102-6437_-102-643 others(6): Show |
GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr14 | 96373229 | |||||
chr14:96373229
|
CA | C | 67 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(64): Show | 167 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.-102-6436delA | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr14 | 96373229 | |||||
chr14:96373229
|
CAA | C | 9 | a0001c0001t0001g0018a0001c0001t0001g0037a0001c0001t0001g0038others(6): Show | 13 | HG01169.hp1 HG02040.hp1 HG02523.hp2 others(10): Show |
intron_variant | MODIFIER | c.-102-6437_-102-643 others(6): Show |
GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr14 | 96373229 | |||||
chr14:96373246
|
AAAAAAAG | A | 5 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0120others(2): Show | 10 | HG02717.hp2 HG02895.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.-102-6438_-102-643 others(11): Show |
GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr14 | 96373246 | |||||
chr14:96373600
|
TA | T | 9 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0118others(6): Show | 14 | HG02145.hp1 HG02293.hp1 HG02717.hp2 others(11): Show |
intron_variant | MODIFIER | c.-102-6076delA | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr14 | 96373600 | |||||
chr14:96373993
|
A | T | 1 | a0001c0001t0001g0104 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-102-5695A>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96373993 | ||||||
chr14:96374024
|
G | A | 1 | a0001c0001t0001g0077 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-102-5664G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96374024 | ||||||
chr14:96374084
|
A | G | 44 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0015others(41): Show | 100 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(97): Show |
intron_variant | MODIFIER | c.-102-5604A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96374084 | ||||||
chr14:96374166
|
T | C | 1 | a0001c0001t0001g0118 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-102-5522T>C | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96374166 | ||||||
chr14:96374183
|
A | G | 1 | a0001c0001t0006g0045 | 2 | HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-102-5505A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96374183 | ||||||
chr14:96374257
|
T | A | 1 | a0001c0001t0003g0147 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-102-5431T>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96374257 | ||||||
chr14:96374258
|
A | T | 1 | a0001c0001t0003g0147 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-102-5430A>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96374258 | ||||||
chr14:96374482
|
A | G | 2 | a0001c0001t0001g0041a0001c0001t0001g0135 | 3 | HG03195.hp1 NA18522.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-102-5206A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96374482 | ||||||
chr14:96374771
|
A | G | 1 | a0001c0001t0001g0098 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-102-4917A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96374771 | ||||||
chr14:96374935
|
CT | C | 5 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0117others(2): Show | 13 | HG00642.hp2 HG01255.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.-102-4751delT | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr14 | 96374935 | |||||
chr14:96375243
|
A | G | 8 | a0001c0001t0001g0018a0001c0001t0001g0037a0001c0001t0001g0038others(5): Show | 12 | HG00621.hp2 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.-102-4445A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96375243 | ||||||
chr14:96375359
|
T | C | 1 | a0001c0001t0003g0148 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-102-4329T>C | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96375359 | ||||||
chr14:96375430
|
T | C | 1 | a0001c0001t0013g0160 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.-102-4258T>C | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96375430 | ||||||
chr14:96375435
|
TC | T | 26 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0039others(23): Show | 65 | HG00099.hp1 HG00408.hp1 HG01099.hp1 others(62): Show |
intron_variant | MODIFIER | c.-102-4252delC | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96375435 | ||||||
chr14:96375436
|
C | CT | 16 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0118others(13): Show | 27 | HG00438.hp1 HG00639.hp1 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.-102-4237dupT | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr14 | 96375436 | |||||
chr14:96375436
|
CT | C | 42 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0015others(39): Show | 97 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.-102-4237delT | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr14 | 96375436 | |||||
chr14:96375459
|
C | T | 1 | a0001c0001t0001g0159 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-102-4229C>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96375459 | ||||||
chr14:96375460
|
G | A | 1 | a0001c0001t0001g0118 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-102-4228G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96375460 | ||||||
chr14:96375494
|
C | T | 1 | a0001c0001t0002g0071 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-102-4194C>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96375494 | ||||||
chr14:96375495
|
G | A | 1 | a0001c0001t0001g0032 | 2 | HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-102-4193G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96375495 | ||||||
chr14:96375520
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-102-4168G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96375520 | ||||||
chr14:96375526
|
C | G | 1 | a0001c0001t0001g0142 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-102-4162C>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96375526 | ||||||
chr14:96375582
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-102-4106C>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96375582 | ||||||
chr14:96375661
|
T | C | 4 | a0001c0001t0001g0078a0001c0001t0001g0163a0001c0001t0006g0045others(1): Show | 5 | HG02486.hp2 HG02922.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-102-4027T>C | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96375661 | ||||||
chr14:96375667
|
C | T | 1 | a0001c0001t0001g0118 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-102-4021C>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96375667 | ||||||
chr14:96375787
|
A | G | 1 | a0001c0001t0001g0080 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-102-3901A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96375787 | ||||||
chr14:96376010
|
A | C | 1 | a0001c0001t0003g0153 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-102-3678A>C | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96376010 | ||||||
chr14:96376308
|
C | T | 4 | a0001c0001t0002g0006a0001c0001t0002g0026a0001c0001t0002g0070others(1): Show | 10 | HG00438.hp1 HG00639.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.-102-3380C>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96376308 | ||||||
chr14:96376339
|
G | GC | 49 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0118others(46): Show | 110 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.-102-3348dupC | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr14 | 96376339 | |||||
chr14:96376369
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-102-3319C>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96376369 | ||||||
chr14:96376470
|
A | G | 1 | a0001c0001t0003g0152 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-102-3218A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96376470 | ||||||
chr14:96376481
|
G | C | 1 | a0001c0001t0001g0041 | 2 | HG03195.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-102-3207G>C | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96376481 | ||||||
chr14:96376510
|
G | A | 8 | a0001c0001t0001g0018a0001c0001t0001g0037a0001c0001t0001g0038others(5): Show | 12 | HG00621.hp2 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.-102-3178G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96376510 | ||||||
chr14:96376627
|
G | A | 2 | a0001c0001t0003g0157a0001c0001t0003g0158 | 2 | NA19054.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.-102-3061G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96376627 | ||||||
chr14:96376822
|
A | G | 1 | a0001c0001t0001g0132 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-102-2866A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96376822 | ||||||
chr14:96376832
|
C | T | 1 | a0001c0001t0001g0131 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-102-2856C>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96376832 | ||||||
chr14:96376928
|
CAAT | C | 28 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0039others(25): Show | 68 | HG00099.hp1 HG00408.hp1 HG01099.hp1 others(65): Show |
intron_variant | MODIFIER | c.-102-2759_-102-275 others(7): Show |
GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96376928 | ||||||
chr14:96377029
|
A | G | 1 | a0001c0001t0001g0114 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-102-2659A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96377029 | ||||||
chr14:96377146
|
A | G | 3 | a0001c0001t0005g0035a0001c0001t0005g0106a0001c0001t0005g0107 | 4 | HG00642.hp1 HG01891.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.-102-2542A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96377146 | ||||||
chr14:96377237
|
A | G | 5 | a0001c0001t0002g0006a0001c0001t0002g0026a0001c0001t0002g0069others(2): Show | 11 | HG00438.hp1 HG00639.hp1 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.-102-2451A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96377237 | ||||||
chr14:96377253
|
G | A | 34 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(31): Show | 82 | HG00099.hp1 HG00408.hp1 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.-102-2435G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96377253 | ||||||
chr14:96377307
|
T | G | 1 | a0001c0001t0003g0149 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-102-2381T>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96377307 | ||||||
chr14:96377435
|
C | T | 1 | a0001c0001t0002g0060 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-102-2253C>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96377435 | ||||||
chr14:96377475
|
G | T | 1 | a0001c0001t0001g0138 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-102-2213G>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96377475 | ||||||
chr14:96377698
|
A | C | 1 | a0001c0001t0001g0095 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-102-1990A>C | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96377698 | ||||||
chr14:96377803
|
C | T | 1 | a0001c0001t0001g0141 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-102-1885C>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96377803 | ||||||
chr14:96377918
|
G | A | 1 | a0001c0001t0003g0042 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-102-1770G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96377918 | ||||||
chr14:96378026
|
T | G | 1 | a0001c0001t0001g0084 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-102-1662T>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96378026 | ||||||
chr14:96378213
|
A | G | 44 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(41): Show | 96 | HG00099.hp1 HG00408.hp1 HG00621.hp2 others(93): Show |
intron_variant | MODIFIER | c.-102-1475A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96378213 | ||||||
chr14:96378228
|
C | T | 44 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0015others(41): Show | 100 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(97): Show |
intron_variant | MODIFIER | c.-102-1460C>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96378228 | ||||||
chr14:96378374
|
T | G | 2 | a0001c0001t0002g0054a0001c0001t0002g0060 | 2 | HG02129.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.-102-1314T>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96378374 | ||||||
chr14:96378503
|
C | A | 1 | a0001c0001t0001g0118 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-102-1185C>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96378503 | ||||||
chr14:96378595
|
T | C | 7 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0118others(4): Show | 12 | HG02145.hp1 HG02717.hp2 HG02895.hp1 others(9): Show |
intron_variant | MODIFIER | c.-102-1093T>C | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96378595 | ||||||
chr14:96378645
|
A | G | 9 | a0001c0001t0001g0018a0001c0001t0001g0037a0001c0001t0001g0038others(6): Show | 13 | HG00621.hp2 HG02040.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.-102-1043A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96378645 | ||||||
chr14:96378737
|
T | C | 2 | a0001c0001t0001g0037a0001c0001t0001g0112 | 3 | HG02735.hp2 HG03239.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-102-951T>C | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96378737 | ||||||
chr14:96378894
|
C | G | 30 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(27): Show | 77 | HG00099.hp1 HG00408.hp1 HG00642.hp2 others(74): Show |
intron_variant | MODIFIER | c.-102-794C>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96378894 | ||||||
chr14:96378981
|
G | A | 3 | a0001c0001t0005g0035a0001c0001t0005g0106a0001c0001t0005g0107 | 4 | HG00642.hp1 HG01891.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.-102-707G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96378981 | ||||||
chr14:96379069
|
G | T | 1 | a0001c0001t0005g0106 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-102-619G>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96379069 | ||||||
chr14:96379108
|
G | A | 1 | a0001c0001t0001g0081 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-102-580G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96379108 | ||||||
chr14:96379196
|
C | T | 3 | a0001c0001t0001g0005a0001c0001t0001g0134a0001c0001t0011g0005 | 10 | NA18948.hp2 NA18956.hp2 NA18957.hp2 others(7): Show |
intron_variant | MODIFIER | c.-102-492C>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96379196 | ||||||
chr14:96379291
|
G | A | 1 | a0001c0001t0002g0072 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-102-397G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96379291 | ||||||
chr14:96379322
|
G | T | 30 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(27): Show | 77 | HG00099.hp1 HG00408.hp1 HG00642.hp2 others(74): Show |
intron_variant | MODIFIER | c.-102-366G>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96379322 | ||||||
chr14:96379488
|
C | G | 2 | a0001c0001t0002g0059a0001c0001t0002g0074 | 2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.-102-200C>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96379488 | ||||||
chr14:96379590
|
A | G | 1 | a0001c0001t0003g0158 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-102-98A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96379590 | ||||||
chr14:96379595
|
C | T | 1 | a0001c0001t0003g0151 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-102-93C>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 1/3 | chr14 | 96379595 | ||||||
chr14:96379898
|
A | G | 1 | a0001c0001t0001g0113 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-2+110A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 2/3 | chr14 | 96379898 | ||||||
chr14:96379944
|
A | G | 8 | a0001c0001t0001g0018a0001c0001t0001g0037a0001c0001t0001g0038others(5): Show | 12 | HG00621.hp2 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.-2+156A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 2/3 | chr14 | 96379944 | ||||||
chr14:96380090
|
A | T | 4 | a0001c0001t0001g0078a0001c0001t0001g0163a0001c0001t0006g0045others(1): Show | 5 | HG02486.hp2 HG02922.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-2+302A>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 2/3 | chr14 | 96380090 | ||||||
chr14:96380238
|
T | G | 1 | a0001c0001t0001g0080 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-2+450T>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 2/3 | chr14 | 96380238 | ||||||
chr14:96380390
|
C | G | 1 | a0001c0001t0001g0118 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-2+602C>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 2/3 | chr14 | 96380390 | ||||||
chr14:96380450
|
CAGG | C | 3 | a0001c0001t0005g0035a0001c0001t0005g0106a0001c0001t0005g0107 | 4 | HG00642.hp1 HG01891.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2+665_-2+667delGA others(1): Show |
GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 96380450 | |||||
chr14:96380474
|
G | T | 1 | a0001c0001t0002g0058 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-2+686G>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 2/3 | chr14 | 96380474 | ||||||
chr14:96380656
|
C | T | 5 | a0001c0001t0001g0009a0001c0001t0001g0119a0001c0001t0001g0120others(2): Show | 8 | HG02145.hp1 HG02895.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-2+868C>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 2/3 | chr14 | 96380656 | ||||||
chr14:96380721
|
G | T | 1 | a0001c0001t0001g0112 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-2+933G>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 2/3 | chr14 | 96380721 | ||||||
chr14:96381003
|
T | C | 41 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0015others(38): Show | 96 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.-2+1215T>C | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 2/3 | chr14 | 96381003 | ||||||
chr14:96381220
|
T | A | 1 | a0001c0001t0001g0090 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-1-1027T>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 2/3 | chr14 | 96381220 | ||||||
chr14:96381348
|
G | T | 8 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(5): Show | 11 | HG02145.hp2 HG02280.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-1-899G>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 2/3 | chr14 | 96381348 | ||||||
chr14:96381360
|
A | T | 1 | a0001c0001t0001g0129 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-1-887A>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 2/3 | chr14 | 96381360 | ||||||
chr14:96381487
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-1-760G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 2/3 | chr14 | 96381487 | ||||||
chr14:96381778
|
C | T | 1 | a0001c0001t0001g0034 | 2 | HG02615.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-1-469C>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 2/3 | chr14 | 96381778 | ||||||
chr14:96381805
|
CTTTTTT | C | 7 | a0001c0001t0001g0018a0001c0001t0001g0037a0001c0001t0001g0038others(4): Show | 11 | HG00621.hp2 HG02040.hp1 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.-1-440_-1-435delTT others(4): Show |
GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 96381805 | |||||
chr14:96381902
|
C | G | 7 | a0001c0001t0001g0018a0001c0001t0001g0037a0001c0001t0001g0038others(4): Show | 11 | HG00621.hp2 HG02040.hp1 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.-1-345C>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 2/3 | chr14 | 96381902 | ||||||
chr14:96381911
|
T | C | 6 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0117others(3): Show | 14 | HG00642.hp2 HG01255.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.-1-336T>C | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 2/3 | chr14 | 96381911 | ||||||
chr14:96381978
|
C | T | 7 | a0001c0001t0001g0018a0001c0001t0001g0037a0001c0001t0001g0038others(4): Show | 11 | HG00621.hp2 HG02040.hp1 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.-1-269C>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 2/3 | chr14 | 96381978 | ||||||
chr14:96381980
|
A | G | 2 | a0001c0001t0001g0041a0001c0001t0001g0135 | 3 | HG03195.hp1 NA18522.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-1-267A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 2/3 | chr14 | 96381980 | ||||||
chr14:96382015
|
G | T | 2 | a0001c0001t0003g0043a0001c0001t0003g0154 | 3 | NA18954.hp2 NA18989.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.-1-232G>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 2/3 | chr14 | 96382015 | ||||||
chr14:96382036
|
G | A | 1 | a0001c0001t0002g0070 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-1-211G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 2/3 | chr14 | 96382036 | ||||||
chr14:96382140
|
T | C | 7 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0118others(4): Show | 12 | HG02145.hp1 HG02717.hp2 HG02895.hp1 others(9): Show |
intron_variant | MODIFIER | c.-1-107T>C | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 2/3 | chr14 | 96382140 | ||||||
chr14:96382195
|
T | C | 1 | a0001c0001t0002g0052 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-1-52T>C | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 2/3 | chr14 | 96382195 | ||||||
chr14:96382228
|
C | CT | 7 | a0001c0001t0001g0016a0001c0001t0001g0078a0001c0001t0001g0085others(4): Show | 11 | HG02109.hp2 HG02486.hp2 HG02922.hp1 others(8): Show |
splice_region_variant&intron_variant | LOW | c.-1-5dupT | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr14 | 96382228 | |||||
chr14:96382562
|
A | G | 24 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0039others(21): Show | 63 | HG00099.hp1 HG00408.hp1 HG01099.hp1 others(60): Show |
intron_variant | MODIFIER | c.258+57A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 3/3 | chr14 | 96382562 | ||||||
chr14:96382567
|
A | C | 1 | a0001c0001t0001g0118 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.258+62A>C | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 3/3 | chr14 | 96382567 | ||||||
chr14:96382606
|
G | A | 2 | a0001c0001t0001g0030a0001c0001t0001g0103 | 3 | HG01261.hp2 HG01496.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.258+101G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 3/3 | chr14 | 96382606 | ||||||
chr14:96382753
|
C | T | 1 | a0001c0001t0001g0033 | 2 | HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.258+248C>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 3/3 | chr14 | 96382753 | ||||||
chr14:96382986
|
A | T | 41 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0015others(38): Show | 96 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.258+481A>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 3/3 | chr14 | 96382986 | ||||||
chr14:96383168
|
G | A | 2 | a0001c0001t0003g0036a0001c0001t0003g0108 | 3 | NA18968.hp2 NA18980.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.258+663G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 3/3 | chr14 | 96383168 | ||||||
chr14:96383212
|
C | G | 7 | a0001c0001t0001g0018a0001c0001t0001g0037a0001c0001t0001g0038others(4): Show | 11 | HG00621.hp2 HG02040.hp1 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.258+707C>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 3/3 | chr14 | 96383212 | ||||||
chr14:96383394
|
T | TA | 24 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0039others(21): Show | 63 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.258+904dupA | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr14 | 96383394 | |||||
chr14:96383394
|
T | TAA | 6 | a0001c0001t0001g0111a0001c0001t0001g0126a0001c0001t0001g0129others(3): Show | 6 | HG01952.hp1 NA18612.hp2 NA18941.hp1 others(3): Show |
intron_variant | MODIFIER | c.258+903_258+904dup others(2): Show |
GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr14 | 96383394 | |||||
chr14:96383394
|
TA | T | 7 | a0001c0001t0001g0078a0001c0001t0001g0093a0001c0001t0001g0163others(4): Show | 8 | HG02486.hp2 HG02922.hp1 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.258+904delA | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr14 | 96383394 | |||||
chr14:96383560
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T | A | 40 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0015others(37): Show | 95 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(92): Show |
intron_variant | MODIFIER | c.258+1055T>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 3/3 | chr14 | 96383560 | ||||||
chr14:96383574
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G | A | 1 | a0001c0001t0001g0092 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.258+1069G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 3/3 | chr14 | 96383574 | ||||||
chr14:96383724
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T | C | 25 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0039others(22): Show | 64 | HG00099.hp1 HG00408.hp1 HG01099.hp1 others(61): Show |
intron_variant | MODIFIER | c.258+1219T>C | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 3/3 | chr14 | 96383724 | ||||||
chr14:96383736
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C | G | 7 | a0001c0001t0001g0018a0001c0001t0001g0037a0001c0001t0001g0038others(4): Show | 11 | HG00621.hp2 HG02040.hp1 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.258+1231C>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 3/3 | chr14 | 96383736 | ||||||
chr14:96383972
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T | G | 8 | a0001c0001t0001g0018a0001c0001t0001g0037a0001c0001t0001g0038others(5): Show | 12 | HG00621.hp2 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.258+1467T>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 3/3 | chr14 | 96383972 | ||||||
chr14:96383998
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G | C | 4 | a0001c0001t0001g0078a0001c0001t0001g0163a0001c0001t0006g0045others(1): Show | 5 | HG02486.hp2 HG02922.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.258+1493G>C | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 3/3 | chr14 | 96383998 | ||||||
chr14:96384035
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A | G | 43 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0008others(40): Show | 99 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.259-1488A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 3/3 | chr14 | 96384035 | ||||||
chr14:96384100
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A | G | 41 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0015others(38): Show | 96 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.259-1423A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 3/3 | chr14 | 96384100 | ||||||
chr14:96384159
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T | C | 24 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0039others(21): Show | 63 | HG00099.hp1 HG00408.hp1 HG01099.hp1 others(60): Show |
intron_variant | MODIFIER | c.259-1364T>C | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 3/3 | chr14 | 96384159 | ||||||
chr14:96384215
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A | G | 3 | a0001c0001t0001g0013a0001c0001t0001g0141a0001c0001t0001g0142 | 6 | HG01255.hp2 HG02559.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.259-1308A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 3/3 | chr14 | 96384215 | ||||||
chr14:96384297
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A | G | 1 | a0001c0001t0002g0046 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.259-1226A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 3/3 | chr14 | 96384297 | ||||||
chr14:96384333
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A | C | 8 | a0001c0001t0001g0018a0001c0001t0001g0037a0001c0001t0001g0038others(5): Show | 12 | HG00621.hp2 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.259-1190A>C | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 3/3 | chr14 | 96384333 | ||||||
chr14:96384391
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AT | A | 8 | a0001c0001t0001g0018a0001c0001t0001g0037a0001c0001t0001g0038others(5): Show | 12 | HG00621.hp2 HG02040.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.259-1129delT | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr14 | 96384391 | |||||
chr14:96384403
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A | G | 2 | a0001c0001t0001g0120a0001c0001t0001g0121 | 2 | HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.259-1120A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 3/3 | chr14 | 96384403 | ||||||
chr14:96384481
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A | G | 1 | a0001c0001t0001g0115 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.259-1042A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 3/3 | chr14 | 96384481 | ||||||
chr14:96384487
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A | C | 1 | a0001c0001t0003g0152 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.259-1036A>C | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 3/3 | chr14 | 96384487 | ||||||
chr14:96384747
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G | A | 1 | a0001c0001t0001g0115 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.259-776G>A | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 3/3 | chr14 | 96384747 | ||||||
chr14:96384774
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C | T | 25 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0039others(22): Show | 64 | HG00099.hp1 HG00408.hp1 HG01099.hp1 others(61): Show |
intron_variant | MODIFIER | c.259-749C>T | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 3/3 | chr14 | 96384774 | ||||||
chr14:96384834
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A | G | 1 | a0001c0001t0002g0057 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.259-689A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 3/3 | chr14 | 96384834 | ||||||
chr14:96384843
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T | C | 138 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(135): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.259-680T>C | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 3/3 | chr14 | 96384843 | ||||||
chr14:96384983
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A | G | 24 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0039others(21): Show | 63 | HG00099.hp1 HG00408.hp1 HG01099.hp1 others(60): Show |
intron_variant | MODIFIER | c.259-540A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 3/3 | chr14 | 96384983 | ||||||
chr14:96384994
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TAAC | T | 2 | a0001c0001t0001g0031a0001c0001t0001g0089 | 3 | HG00639.hp2 HG02258.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.259-525_259-523del others(3): Show |
GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr14 | 96384994 | |||||
chr14:96384995
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A | G | 1 | a0001c0001t0002g0056 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.259-528A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 3/3 | chr14 | 96384995 | ||||||
chr14:96384999
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A | G | 1 | a0001c0001t0001g0115 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.259-524A>G | GSKIP | ENSG00000100744.15 | transcript | ENST00000555181.6 | protein_coding | 3/3 | chr14 | 96384999 |