geneid | 348654 |
---|---|
ensemblid | ENSG00000178295.15 |
hgncid | 26881 |
symbol | GEN1 |
name | GEN1 Holliday junction 5' flap endonuclease |
refseq_nuc | NM_001130009.3 |
refseq_prot | NP_001123481.3 |
ensembl_nuc | ENST00000381254.7 |
ensembl_prot | ENSP00000370653.2 |
mane_status | MANE Select |
chr | chr2 |
start | 17754138 |
end | 17788946 |
strand | + |
ver | v1.2 |
region | chr2:17754138-17788946 |
region5000 | chr2:17749138-17793946 |
regionname0 | GEN1_chr2_17754138_17788946 |
regionname5000 | GEN1_chr2_17749138_17793946 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 908 | 134 | 8 | 22 | 76 | 8 | 20 | 58 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0002 | 0/0 | 908 | 49 | 19 | 14 | 5 | 7 | 4 | 4 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0003 | 0/0 | 908 | 38 | 21 | 6 | 7 | 2 | 2 | 6 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0004 | 0/0 | 839 | 30 | 2 | 8 | 17 | 1 | 2 | 10 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0005 | 0/0 | 908 | 16 | 0 | 1 | 15 | 0 | 0 | 14 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0006 | 0/0 | 908 | 13 | 13 | 0 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0007 | 0/0 | 908 | 9 | 9 | 0 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0008 | 0/0 | 908 | 7 | 6 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0009 | 0/0 | 908 | 7 | 0 | 4 | 0 | 0 | 3 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0010 | 0/0 | 908 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0011 | 0/0 | 908 | 3 | 0 | 0 | 0 | 0 | 3 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0012 | 0/0 | 908 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0013 | 0/0 | 908 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0014 | 0/0 | 908 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0015 | 0/0 | 908 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0016 | 0/0 | 908 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0017 | 0/0 | 908 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 2727 | 131 | 6 | 22 | 76 | 8 | 19 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
c0002 | 0/0 | 2727 | 49 | 19 | 14 | 5 | 7 | 4 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
c0003 | 0/0 | 2727 | 37 | 21 | 6 | 7 | 1 | 2 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
c0004 | 0/0 | 2722 | 30 | 2 | 8 | 17 | 1 | 2 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
c0005 | 0/0 | 2727 | 16 | 0 | 1 | 15 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
c0006 | 0/0 | 2727 | 13 | 13 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
c0007 | 0/0 | 2727 | 9 | 9 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
c0008 | 0/0 | 2727 | 7 | 6 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
c0009 | 0/0 | 2727 | 6 | 0 | 3 | 0 | 0 | 3 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
c0010 | 0/0 | 2727 | 6 | 6 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
c0011 | 0/0 | 2727 | 3 | 0 | 0 | 0 | 0 | 3 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
c0012 | 0/0 | 2727 | 2 | 2 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
c0013 | 0/0 | 2727 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
c0014 | 0/0 | 2727 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
c0015 | 0/0 | 2727 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
c0016 | 0/0 | 2727 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
c0017 | 0/0 | 2727 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
c0018 | 0/0 | 2727 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
c0019 | 0/0 | 2727 | 1 | 0 | 0 | 0 | 1 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
c0020 | 0/0 | 2727 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
c0021 | 0/0 | 2727 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 7232 | 130 | 7 | 28 | 70 | 5 | 20 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
t0002 | 0/0 | 7231 | 50 | 23 | 13 | 3 | 7 | 4 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
t0003 | 0/0 | 7232 | 21 | 13 | 5 | 0 | 1 | 2 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
t0004 | 0/0 | 7232 | 14 | 0 | 0 | 14 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
t0005 | 0/0 | 7227 | 12 | 0 | 0 | 12 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
t0006 | 0/0 | 7232 | 8 | 3 | 0 | 4 | 1 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
t0007 | 0/0 | 7231 | 6 | 6 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
t0008 | 0/0 | 7227 | 5 | 3 | 0 | 2 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
t0009 | 0/0 | 7232 | 5 | 1 | 0 | 0 | 3 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
t0010 | 0/0 | 7227 | 4 | 4 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
t0011 | 0/0 | 7227 | 4 | 4 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
t0012 | 0/0 | 7231 | 4 | 3 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
t0013 | 0/0 | 7232 | 3 | 0 | 0 | 3 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
t0014 | 0/0 | 7232 | 3 | 1 | 0 | 0 | 1 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
t0015 | 0/0 | 7232 | 3 | 0 | 0 | 0 | 0 | 3 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
t0016 | 0/0 | 7231 | 2 | 2 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
t0017 | 0/0 | 7231 | 2 | 2 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
t0018 | 0/0 | 7232 | 2 | 2 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
t0019 | 0/0 | 7232 | 2 | 0 | 0 | 0 | 0 | 2 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
t0020 | 0/0 | 7232 | 2 | 0 | 2 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
t0021 | 0/0 | 7232 | 2 | 0 | 2 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
t0022 | 0/0 | 7231 | 2 | 0 | 0 | 2 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
t0023 | 0/0 | 7232 | 2 | 0 | 2 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
t0024 | 0/0 | 7232 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
t0025 | 0/0 | 7232 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
t0026 | 0/0 | 7227 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
t0027 | 0/0 | 7227 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
t0028 | 0/0 | 7227 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
t0029 | 0/0 | 7227 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
t0030 | 0/0 | 7232 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
t0031 | 0/0 | 7232 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
t0032 | 0/0 | 6526 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
t0033 | 0/0 | 7231 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
t0034 | 0/0 | 7232 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
t0035 | 0/0 | 7232 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
t0036 | 0/0 | 7232 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
t0037 | 0/0 | 7232 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
t0038 | 0/0 | 7232 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
t0039 | 0/0 | 7232 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
t0040 | 0/0 | 7231 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
t0041 | 0/0 | 7231 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
t0042 | 0/0 | 7231 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
t0043 | 0/0 | 7231 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
t0044 | 0/0 | 7232 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
t0045 | 0/0 | 7231 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
t0046 | 0/0 | 7231 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
t0047 | 0/0 | 7232 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
t0048 | 0/0 | 7232 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
t0049 | 0/0 | 7232 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
t0050 | 0/0 | 7232 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
t0051 | 0/0 | 7232 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
t0052 | 0/0 | 7232 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
t0053 | 0/0 | 7232 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 23 | 0 | 4 | 16 | 0 | 3 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0002 | 0/0 | 14 | 0 | 1 | 13 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0003 | 0/0 | 8 | 1 | 2 | 4 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0004 | 0/0 | 6 | 0 | 0 | 3 | 0 | 3 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0009 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0010 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0011 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0013 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0014 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0015 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0016 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0020 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0021 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0037 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0040 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 2727 | 131 | 6 | 22 | 76 | 8 | 19 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0001c0012 | 0/0 | 2727 | 2 | 2 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0001c0020 | 0/0 | 2727 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0002c0002 | 0/0 | 2727 | 49 | 19 | 14 | 5 | 7 | 4 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0003c0003 | 0/0 | 2727 | 37 | 21 | 6 | 7 | 1 | 2 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0003c0019 | 0/0 | 2727 | 1 | 0 | 0 | 0 | 1 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0004c0004 | 0/0 | 2722 | 30 | 2 | 8 | 17 | 1 | 2 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0005c0005 | 0/0 | 2727 | 16 | 0 | 1 | 15 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0006c0006 | 0/0 | 2727 | 13 | 13 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0007c0007 | 0/0 | 2727 | 9 | 9 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0008c0008 | 0/0 | 2727 | 7 | 6 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0009c0009 | 0/0 | 2727 | 6 | 0 | 3 | 0 | 0 | 3 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0009c0018 | 0/0 | 2727 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0010c0010 | 0/0 | 2727 | 6 | 6 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0011c0011 | 0/0 | 2727 | 3 | 0 | 0 | 0 | 0 | 3 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0012c0013 | 0/0 | 2727 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0013c0021 | 0/0 | 2727 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0014c0016 | 0/0 | 2727 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0015c0015 | 0/0 | 2727 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0016c0017 | 0/0 | 2727 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0017c0014 | 0/0 | 2727 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 9958 | 99 | 4 | 22 | 54 | 4 | 15 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0001c0001t0004 | 0/0 | 9958 | 14 | 0 | 0 | 14 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0001c0001t0009 | 0/0 | 9958 | 5 | 1 | 0 | 0 | 3 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0001c0001t0014 | 0/0 | 9958 | 3 | 1 | 0 | 0 | 1 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0001c0001t0030 | 0/0 | 9958 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0001c0001t0031 | 0/0 | 9958 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0001c0001t0034 | 0/0 | 9958 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0001c0001t0035 | 0/0 | 9958 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0001c0001t0036 | 0/0 | 9958 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0001c0001t0037 | 0/0 | 9958 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0001c0001t0038 | 0/0 | 9958 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0001c0001t0044 | 0/0 | 9958 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0001c0001t0051 | 0/0 | 9958 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0001c0001t0053 | 0/0 | 9958 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0001c0012t0018 | 0/0 | 9958 | 2 | 2 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0001c0020t0001 | 0/0 | 9958 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0002c0002t0002 | 0/0 | 9957 | 37 | 11 | 12 | 3 | 7 | 4 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0002c0002t0007 | 0/0 | 9957 | 6 | 6 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0002c0002t0022 | 0/0 | 9957 | 2 | 0 | 0 | 2 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0002c0002t0042 | 0/0 | 9957 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0002c0002t0043 | 0/0 | 9957 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0002c0002t0045 | 0/0 | 9957 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0002c0002t0046 | 0/0 | 9957 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0003c0003t0003 | 0/0 | 9958 | 17 | 13 | 3 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0003c0003t0006 | 0/0 | 9958 | 8 | 3 | 0 | 4 | 1 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0003c0003t0013 | 0/0 | 9958 | 3 | 0 | 0 | 3 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0003c0003t0020 | 0/0 | 9958 | 2 | 0 | 2 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0003c0003t0024 | 0/0 | 9958 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0003c0003t0025 | 0/0 | 9958 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0003c0003t0047 | 0/0 | 9958 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0003c0003t0048 | 0/0 | 9958 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0003c0003t0049 | 0/0 | 9958 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0003c0003t0050 | 0/0 | 9958 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0003c0003t0052 | 0/0 | 9958 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0003c0019t0003 | 0/0 | 9958 | 1 | 0 | 0 | 0 | 1 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0004c0004t0001 | 0/0 | 9953 | 27 | 2 | 6 | 16 | 1 | 2 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0004c0004t0023 | 0/0 | 9953 | 2 | 0 | 2 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0004c0004t0039 | 0/0 | 9953 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0005c0005t0005 | 0/0 | 9953 | 12 | 0 | 0 | 12 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0005c0005t0008 | 0/0 | 9953 | 2 | 0 | 0 | 2 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0005c0005t0027 | 0/0 | 9953 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0005c0005t0029 | 0/0 | 9953 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0006c0006t0008 | 0/0 | 9953 | 3 | 3 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0006c0006t0010 | 0/0 | 9953 | 4 | 4 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0006c0006t0011 | 0/0 | 9953 | 4 | 4 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0006c0006t0026 | 0/0 | 9953 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0006c0006t0028 | 0/0 | 9953 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0007c0007t0002 | 0/0 | 9957 | 5 | 5 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0007c0007t0017 | 0/0 | 9957 | 2 | 2 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0007c0007t0032 | 0/0 | 9252 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0007c0007t0033 | 0/0 | 9957 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0008c0008t0002 | 0/0 | 9957 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0008c0008t0012 | 0/0 | 9957 | 3 | 2 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0008c0008t0016 | 0/0 | 9957 | 2 | 2 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0008c0008t0041 | 0/0 | 9957 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0009c0009t0003 | 0/0 | 9958 | 2 | 0 | 1 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0009c0009t0019 | 0/0 | 9958 | 2 | 0 | 0 | 0 | 0 | 2 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0009c0009t0021 | 0/0 | 9958 | 2 | 0 | 2 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0009c0018t0003 | 0/0 | 9958 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0010c0010t0002 | 0/0 | 9957 | 6 | 6 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0011c0011t0015 | 0/0 | 9958 | 3 | 0 | 0 | 0 | 0 | 3 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0012c0013t0012 | 0/0 | 9957 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0013c0021t0002 | 0/0 | 9957 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0014c0016t0001 | 0/0 | 9958 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0015c0015t0040 | 0/0 | 9957 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0016c0017t0001 | 0/0 | 9958 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
a0017c0014t0001 | 0/0 | 9958 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | copy fasta | chr2 | 17749138 | 17793946 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 11 | 0 | 4 | 7 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0001g0004 | 0/0 | 5 | 0 | 0 | 3 | 0 | 2 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0001g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0001g0014 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0001g0016 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0001g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0004g0001 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0004g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0004g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0004g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0004g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0004g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0004g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0009g0015 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0009g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0009g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0009g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0014g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0014g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0014g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0030g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0031g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0034g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0035g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0036g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0037g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0038g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0044g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0051g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0001t0053g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0012t0018g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0001c0020t0001g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0002c0002t0002g0009 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0002c0002t0002g0010 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0002c0002t0002g0011 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0002c0002t0002g0020 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0002c0002t0002g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0002c0002t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0002c0002t0002g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0002c0002t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0002c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0002c0002t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0002c0002t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0002c0002t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0002c0002t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0002c0002t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0002c0002t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0002c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0002c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0002c0002t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0002c0002t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0002c0002t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0002c0002t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0002c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0002c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0002c0002t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0002c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0002c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0002c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0002c0002t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0002c0002t0007g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0002c0002t0007g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0002c0002t0007g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0002c0002t0022g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0002c0002t0042g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0002c0002t0043g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0002c0002t0045g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0002c0002t0046g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0003c0003t0003g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0003c0003t0003g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0003c0003t0003g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0003c0003t0003g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0003c0003t0003g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0003c0003t0003g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0003c0003t0003g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0003c0003t0003g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0003c0003t0003g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0003c0003t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0003c0003t0003g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0003c0003t0003g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0003c0003t0003g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0003c0003t0003g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0003c0003t0006g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0003c0003t0006g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0003c0003t0006g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0003c0003t0006g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0003c0003t0006g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0003c0003t0006g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0003c0003t0006g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0003c0003t0013g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0003c0003t0013g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0003c0003t0013g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0003c0003t0020g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0003c0003t0024g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0003c0003t0025g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0003c0003t0047g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0003c0003t0048g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0003c0003t0049g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0003c0003t0050g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0003c0003t0052g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0003c0019t0003g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0004c0004t0001g0003 | 0/0 | 8 | 1 | 2 | 4 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0004c0004t0001g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0004c0004t0001g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0004c0004t0001g0040 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0004c0004t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0004c0004t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0004c0004t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0004c0004t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0004c0004t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0004c0004t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0004c0004t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0004c0004t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0004c0004t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0004c0004t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0004c0004t0023g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0004c0004t0023g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0004c0004t0039g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0005c0005t0005g0002 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0005c0005t0005g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0005c0005t0008g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0005c0005t0027g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0005c0005t0029g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0006c0006t0008g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0006c0006t0008g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0006c0006t0010g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0006c0006t0010g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0006c0006t0011g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0006c0006t0011g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0006c0006t0011g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0006c0006t0026g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0006c0006t0028g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0007c0007t0002g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0007c0007t0002g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0007c0007t0017g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0007c0007t0017g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0007c0007t0032g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0007c0007t0033g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0008c0008t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0008c0008t0012g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0008c0008t0012g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0008c0008t0012g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0008c0008t0016g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0008c0008t0041g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0009c0009t0003g0021 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0009c0009t0019g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0009c0009t0019g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0009c0009t0021g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0009c0018t0003g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0010c0010t0002g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0010c0010t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0010c0010t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0010c0010t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0010c0010t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0011c0011t0015g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0011c0011t0015g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0011c0011t0015g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0012c0013t0012g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0013c0021t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0014c0016t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0015c0015t0040g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0016c0017t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
a0017c0014t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0206 | EUR | GBR | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG00099 | hp2 | a0001 | c0001 | t0009 | g0015 | EUR | GBR | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG00140 | hp1 | a0003 | c0019 | t0003 | g0068 | EUR | GBR | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG00140 | hp2 | a0002 | c0002 | t0002 | g0091 | EUR | GBR | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG00280 | hp1 | a0001 | c0001 | t0009 | g0139 | EUR | FIN | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG00280 | hp2 | a0002 | c0002 | t0002 | g0086 | EUR | FIN | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0190 | EUR | FIN | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG00323 | hp2 | a0002 | c0002 | t0002 | g0010 | EUR | FIN | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG00408 | hp1 | a0004 | c0004 | t0001 | g0006 | EAS | CHS | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | CHS | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG00423 | hp1 | a0004 | c0004 | t0001 | g0193 | EAS | CHS | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG00423 | hp2 | a0001 | c0001 | t0034 | g0001 | EAS | CHS | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | CHS | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG00438 | hp2 | a0004 | c0004 | t0001 | g0006 | EAS | CHS | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG00558 | hp1 | a0004 | c0004 | t0001 | g0204 | EAS | CHS | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG00621 | hp1 | a0004 | c0004 | t0001 | g0003 | EAS | CHS | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG00621 | hp2 | a0005 | c0005 | t0008 | g0002 | EAS | CHS | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG00639 | hp1 | a0003 | c0003 | t0020 | g0013 | AMR | PUR | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG00639 | hp2 | a0005 | c0005 | t0029 | g0002 | AMR | PUR | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG00642 | hp1 | a0004 | c0004 | t0023 | g0144 | AMR | PUR | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG00642 | hp2 | a0002 | c0002 | t0045 | g0084 | AMR | PUR | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG00735 | hp1 | a0013 | c0021 | t0002 | g0081 | AMR | PUR | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG00735 | hp2 | a0004 | c0004 | t0001 | g0003 | AMR | PUR | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG00738 | hp1 | a0004 | c0004 | t0001 | g0040 | AMR | PUR | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG00738 | hp2 | a0002 | c0002 | t0002 | g0102 | AMR | PUR | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG00741 | hp1 | a0004 | c0004 | t0001 | g0205 | AMR | PUR | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG01069 | hp1 | a0009 | c0009 | t0021 | g0022 | AMR | PUR | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG01069 | hp2 | a0015 | c0015 | t0040 | g0121 | AMR | PUR | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG01070 | hp2 | a0009 | c0018 | t0003 | g0050 | AMR | PUR | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG01071 | hp2 | a0009 | c0009 | t0021 | g0022 | AMR | PUR | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG01074 | hp1 | a0004 | c0004 | t0001 | g0003 | AMR | PUR | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG01074 | hp2 | a0003 | c0003 | t0020 | g0013 | AMR | PUR | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG01099 | hp2 | a0002 | c0002 | t0002 | g0082 | AMR | PUR | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG01106 | hp1 | a0004 | c0004 | t0001 | g0039 | AMR | PUR | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG01109 | hp1 | a0002 | c0002 | t0002 | g0097 | AMR | PUR | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG01109 | hp2 | a0008 | c0008 | t0012 | g0104 | AMR | PUR | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG01168 | hp1 | a0002 | c0002 | t0002 | g0009 | AMR | PUR | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG01175 | hp1 | a0002 | c0002 | t0002 | g0090 | AMR | PUR | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG01175 | hp2 | a0004 | c0004 | t0023 | g0148 | AMR | PUR | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG01192 | hp1 | a0004 | c0004 | t0001 | g0039 | AMR | PUR | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG01192 | hp2 | a0002 | c0002 | t0042 | g0032 | AMR | PUR | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG01243 | hp1 | a0003 | c0003 | t0003 | g0059 | AMR | PUR | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG01256 | hp1 | a0002 | c0002 | t0002 | g0032 | AMR | CLM | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG01261 | hp1 | a0003 | c0003 | t0003 | g0061 | AMR | CLM | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | CLM | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG01346 | hp1 | a0002 | c0002 | t0002 | g0009 | AMR | CLM | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | CLM | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG01358 | hp1 | a0002 | c0002 | t0002 | g0010 | AMR | CLM | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | CLM | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG01433 | hp1 | a0009 | c0009 | t0003 | g0021 | AMR | CLM | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG01433 | hp2 | a0002 | c0002 | t0002 | g0011 | AMR | CLM | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG01496 | hp1 | a0003 | c0003 | t0049 | g0049 | AMR | CLM | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG01515 | hp1 | a0002 | c0002 | t0002 | g0020 | EUR | IBS | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG01515 | hp2 | a0002 | c0002 | t0002 | g0009 | EUR | IBS | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG01516 | hp1 | a0002 | c0002 | t0002 | g0011 | EUR | IBS | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0014 | EUR | IBS | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG01517 | hp1 | a0002 | c0002 | t0002 | g0020 | EUR | IBS | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0014 | EUR | IBS | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG01884 | hp1 | a0003 | c0003 | t0006 | g0067 | AFR | ACB | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG01884 | hp2 | a0003 | c0003 | t0048 | g0056 | AFR | ACB | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG01891 | hp1 | a0002 | c0002 | t0002 | g0026 | AFR | ACB | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG01891 | hp2 | a0003 | c0003 | t0003 | g0007 | AFR | ACB | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG01934 | hp1 | a0003 | c0003 | t0003 | g0053 | AMR | PEL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG01981 | hp1 | a0002 | c0002 | t0002 | g0030 | AMR | PEL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG02004 | hp1 | a0002 | c0002 | t0002 | g0030 | AMR | PEL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG02015 | hp1 | a0004 | c0004 | t0001 | g0003 | EAS | KHV | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG02027 | hp1 | a0001 | c0001 | t0030 | g0198 | EAS | KHV | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | KHV | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG02055 | hp1 | a0002 | c0002 | t0007 | g0008 | AFR | ACB | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG02055 | hp2 | a0001 | c0001 | t0009 | g0140 | AFR | ACB | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG02056 | hp2 | a0003 | c0003 | t0006 | g0024 | EAS | KHV | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | KHV | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG02145 | hp1 | a0003 | c0003 | t0003 | g0111 | AFR | ACB | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG02145 | hp2 | a0003 | c0003 | t0006 | g0064 | AFR | ACB | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | CDX | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | CDX | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG02257 | hp1 | a0002 | c0002 | t0002 | g0078 | AFR | ACB | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG02257 | hp2 | a0006 | c0006 | t0010 | g0214 | AFR | ACB | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG02258 | hp1 | a0004 | c0004 | t0001 | g0003 | AFR | ACB | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG02258 | hp2 | a0008 | c0008 | t0016 | g0033 | AFR | ACB | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | PEL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PEL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG02280 | hp1 | a0002 | c0002 | t0002 | g0076 | AFR | ACB | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG02280 | hp2 | a0006 | c0006 | t0010 | g0018 | AFR | ACB | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG02300 | hp1 | a0002 | c0002 | t0002 | g0011 | AMR | PEL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG02451 | hp1 | a0006 | c0006 | t0028 | g0114 | AFR | ACB | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG02451 | hp2 | a0003 | c0003 | t0003 | g0023 | AFR | ACB | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | KHV | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG02572 | hp1 | a0001 | c0012 | t0018 | g0019 | AFR | GWD | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG02572 | hp2 | a0014 | c0016 | t0001 | g0145 | AFR | GWD | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0191 | SAS | PJL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG02602 | hp2 | a0004 | c0004 | t0001 | g0194 | SAS | PJL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG02615 | hp1 | a0007 | c0007 | t0002 | g0012 | AFR | GWD | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG02615 | hp2 | a0006 | c0006 | t0026 | g0212 | AFR | GWD | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG02622 | hp1 | a0007 | c0007 | t0033 | g0108 | AFR | GWD | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG02622 | hp2 | a0002 | c0002 | t0002 | g0080 | AFR | GWD | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG02630 | hp1 | a0006 | c0006 | t0010 | g0018 | AFR | GWD | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG02630 | hp2 | a0007 | c0007 | t0002 | g0012 | AFR | GWD | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG02717 | hp2 | a0010 | c0010 | t0002 | g0028 | AFR | GWD | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG02723 | hp1 | a0002 | c0002 | t0002 | g0089 | AFR | GWD | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG02723 | hp2 | a0007 | c0007 | t0002 | g0025 | AFR | GWD | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG02738 | hp1 | a0001 | c0001 | t0009 | g0142 | SAS | PJL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG02809 | hp1 | a0007 | c0007 | t0002 | g0012 | AFR | GWD | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG02809 | hp2 | a0003 | c0003 | t0003 | g0047 | AFR | GWD | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG02886 | hp1 | a0008 | c0008 | t0041 | g0045 | AFR | GWD | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG02886 | hp2 | a0012 | c0013 | t0012 | g0103 | AFR | GWD | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG02896 | hp1 | a0002 | c0002 | t0002 | g0026 | AFR | GWD | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG02896 | hp2 | a0006 | c0006 | t0008 | g0034 | AFR | GWD | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG02922 | hp1 | a0008 | c0008 | t0016 | g0033 | AFR | ESN | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG02922 | hp2 | a0003 | c0003 | t0003 | g0057 | AFR | ESN | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG02965 | hp1 | a0008 | c0008 | t0012 | g0105 | AFR | ESN | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG02965 | hp2 | a0006 | c0006 | t0011 | g0211 | AFR | ESN | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG02970 | hp1 | a0006 | c0006 | t0011 | g0044 | AFR | ESN | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG02970 | hp2 | a0002 | c0002 | t0007 | g0008 | AFR | ESN | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG02976 | hp1 | a0003 | c0003 | t0003 | g0023 | AFR | ESN | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG02976 | hp2 | a0010 | c0010 | t0002 | g0028 | AFR | ESN | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG03041 | hp1 | a0010 | c0010 | t0002 | g0093 | AFR | GWD | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG03041 | hp2 | a0002 | c0002 | t0007 | g0027 | AFR | GWD | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG03098 | hp1 | a0002 | c0002 | t0002 | g0029 | AFR | MSL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG03098 | hp2 | a0006 | c0006 | t0008 | g0115 | AFR | MSL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG03130 | hp1 | a0003 | c0003 | t0050 | g0058 | AFR | ESN | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG03130 | hp2 | a0007 | c0007 | t0017 | g0110 | AFR | ESN | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG03139 | hp1 | a0003 | c0003 | t0003 | g0007 | AFR | ESN | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG03139 | hp2 | a0002 | c0002 | t0007 | g0008 | AFR | ESN | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG03195 | hp1 | a0003 | c0003 | t0003 | g0007 | AFR | ESN | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG03195 | hp2 | a0006 | c0006 | t0010 | g0018 | AFR | ESN | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG03209 | hp1 | a0002 | c0002 | t0007 | g0027 | AFR | MSL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG03209 | hp2 | a0002 | c0002 | t0002 | g0077 | AFR | MSL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG03225 | hp1 | a0001 | c0012 | t0018 | g0019 | AFR | MSL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | MSL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG03239 | hp1 | a0002 | c0002 | t0002 | g0048 | SAS | PJL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG03239 | hp2 | a0009 | c0009 | t0019 | g0051 | SAS | PJL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG03453 | hp1 | a0010 | c0010 | t0002 | g0094 | AFR | MSL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | MSL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG03492 | hp1 | a0001 | c0001 | t0014 | g0015 | SAS | PJL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG03516 | hp1 | a0003 | c0003 | t0052 | g0063 | AFR | ESN | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG03516 | hp2 | a0002 | c0002 | t0007 | g0075 | AFR | ESN | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG03540 | hp1 | a0002 | c0002 | t0002 | g0079 | AFR | GWD | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG03540 | hp2 | a0007 | c0007 | t0017 | g0109 | AFR | GWD | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG03579 | hp1 | a0003 | c0003 | t0003 | g0060 | AFR | MSL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG03579 | hp2 | a0002 | c0002 | t0002 | g0088 | AFR | MSL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG03654 | hp1 | a0002 | c0002 | t0002 | g0098 | SAS | PJL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG03654 | hp2 | a0017 | c0014 | t0001 | g0001 | SAS | PJL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG03669 | hp1 | a0011 | c0011 | t0015 | g0074 | SAS | PJL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG03669 | hp2 | a0004 | c0004 | t0001 | g0003 | SAS | PJL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | STU | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG03688 | hp2 | a0001 | c0020 | t0001 | g0004 | SAS | STU | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG03704 | hp1 | a0009 | c0009 | t0003 | g0021 | SAS | PJL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG03710 | hp1 | a0009 | c0009 | t0019 | g0052 | SAS | PJL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG03831 | hp1 | a0001 | c0001 | t0044 | g0001 | SAS | BEB | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG03831 | hp2 | a0001 | c0001 | t0036 | g0135 | SAS | BEB | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG03834 | hp1 | a0002 | c0002 | t0002 | g0085 | SAS | BEB | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG03834 | hp2 | a0016 | c0017 | t0001 | g0001 | SAS | BEB | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | BEB | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | BEB | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG04199 | hp1 | a0011 | c0011 | t0015 | g0072 | SAS | STU | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | STU | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG04204 | hp1 | a0011 | c0011 | t0015 | g0073 | SAS | STU | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG04204 | hp2 | a0003 | c0003 | t0025 | g0071 | SAS | STU | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | STU | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG04228 | hp2 | a0002 | c0002 | t0002 | g0092 | SAS | STU | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA18522 | hp1 | a0008 | c0008 | t0012 | g0106 | AFR | YRI | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA18522 | hp2 | a0010 | c0010 | t0002 | g0095 | AFR | YRI | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | CHB | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA18612 | hp2 | a0004 | c0004 | t0001 | g0006 | EAS | CHB | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA18747 | hp1 | a0002 | c0002 | t0002 | g0010 | EAS | CHB | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | CHB | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA18906 | hp1 | a0006 | c0006 | t0011 | g0044 | AFR | YRI | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA18906 | hp2 | a0003 | c0003 | t0003 | g0046 | AFR | YRI | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA18939 | hp1 | a0004 | c0004 | t0001 | g0203 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA18945 | hp1 | a0004 | c0004 | t0001 | g0006 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA18945 | hp2 | a0005 | c0005 | t0005 | g0002 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA18946 | hp1 | a0001 | c0001 | t0053 | g0185 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA18946 | hp2 | a0005 | c0005 | t0027 | g0113 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA18952 | hp2 | a0004 | c0004 | t0001 | g0192 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA18954 | hp2 | a0004 | c0004 | t0001 | g0003 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA18957 | hp1 | a0005 | c0005 | t0005 | g0002 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA18959 | hp1 | a0003 | c0003 | t0013 | g0118 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA18964 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA18964 | hp2 | a0004 | c0004 | t0001 | g0041 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA18967 | hp1 | a0001 | c0001 | t0037 | g0189 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA18967 | hp2 | a0003 | c0003 | t0013 | g0120 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA18968 | hp1 | a0001 | c0001 | t0038 | g0149 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA18968 | hp2 | a0005 | c0005 | t0005 | g0002 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA18970 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA18970 | hp2 | a0004 | c0004 | t0001 | g0041 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA18971 | hp2 | a0005 | c0005 | t0005 | g0002 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA18972 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA18977 | hp2 | a0005 | c0005 | t0008 | g0002 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA18978 | hp1 | a0003 | c0003 | t0006 | g0024 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA18979 | hp1 | a0005 | c0005 | t0005 | g0002 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA18979 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA18980 | hp1 | a0001 | c0001 | t0004 | g0146 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA18982 | hp1 | a0001 | c0001 | t0004 | g0167 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA18982 | hp2 | a0004 | c0004 | t0001 | g0003 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA18984 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA18984 | hp2 | a0005 | c0005 | t0005 | g0002 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA18986 | hp1 | a0001 | c0001 | t0035 | g0152 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA18989 | hp1 | a0003 | c0003 | t0013 | g0119 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA18992 | hp2 | a0005 | c0005 | t0005 | g0002 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA18993 | hp1 | a0001 | c0001 | t0031 | g0158 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA18993 | hp2 | a0004 | c0004 | t0001 | g0042 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA18997 | hp1 | a0001 | c0001 | t0051 | g0143 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA18997 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA19001 | hp1 | a0005 | c0005 | t0005 | g0112 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA19004 | hp2 | a0003 | c0003 | t0006 | g0066 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA19006 | hp1 | a0005 | c0005 | t0005 | g0002 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA19010 | hp2 | a0004 | c0004 | t0039 | g0042 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA19012 | hp1 | a0005 | c0005 | t0005 | g0002 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA19012 | hp2 | a0001 | c0001 | t0004 | g0151 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA19030 | hp1 | a0003 | c0003 | t0006 | g0069 | AFR | LWK | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA19030 | hp2 | a0006 | c0006 | t0011 | g0213 | AFR | LWK | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA19043 | hp1 | a0006 | c0006 | t0008 | g0034 | AFR | LWK | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA19043 | hp2 | a0003 | c0003 | t0024 | g0116 | AFR | LWK | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA19057 | hp1 | a0002 | c0002 | t0002 | g0099 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA19057 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA19060 | hp1 | a0001 | c0001 | t0004 | g0183 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA19060 | hp2 | a0004 | c0004 | t0001 | g0196 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA19064 | hp1 | a0005 | c0005 | t0005 | g0002 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA19067 | hp1 | a0002 | c0002 | t0022 | g0031 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA19067 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA19070 | hp2 | a0005 | c0005 | t0005 | g0002 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA19076 | hp1 | a0003 | c0003 | t0006 | g0065 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA19077 | hp1 | a0001 | c0001 | t0004 | g0184 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA19077 | hp2 | a0002 | c0002 | t0002 | g0100 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA19089 | hp1 | a0001 | c0001 | t0004 | g0150 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA19240 | hp1 | a0002 | c0002 | t0046 | g0083 | AFR | YRI | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA19240 | hp2 | a0010 | c0010 | t0002 | g0096 | AFR | YRI | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA20129 | hp1 | a0003 | c0003 | t0003 | g0013 | AFR | ASW | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA20129 | hp2 | a0007 | c0007 | t0032 | g0107 | AFR | ASW | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA20752 | hp1 | a0001 | c0001 | t0009 | g0015 | EUR | TSI | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA20752 | hp2 | a0003 | c0003 | t0006 | g0070 | EUR | TSI | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA20805 | hp1 | a0004 | c0004 | t0001 | g0040 | EUR | TSI | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA20805 | hp2 | a0001 | c0001 | t0014 | g0202 | EUR | TSI | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA20905 | hp1 | a0003 | c0003 | t0003 | g0062 | SAS | GIH | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | GIH | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG02486 | hp1 | a0003 | c0003 | t0047 | g0054 | AFR | ACB | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG02486 | hp2 | a0008 | c0008 | t0002 | g0101 | AFR | ACB | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG02559 | hp1 | a0002 | c0002 | t0002 | g0087 | AFR | ACB | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG02559 | hp2 | a0007 | c0007 | t0002 | g0025 | AFR | ACB | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG03471 | hp1 | a0003 | c0003 | t0003 | g0055 | AFR | MSL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG03471 | hp2 | a0002 | c0002 | t0043 | g0029 | AFR | MSL | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG06807 | hp1 | a0004 | c0004 | t0001 | g0195 | AFR | USA | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
HG06807 | hp2 | a0003 | c0003 | t0003 | g0117 | AFR | USA | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA18955 | hp1 | a0002 | c0002 | t0022 | g0031 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA21309 | hp1 | a0001 | c0001 | t0014 | g0141 | AFR | LWK | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | LWK | GEN1_chr2_17749138_17793946 | GEN1 | chr2 | 17749138 | 17793946 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:17760083
|
G | A | 1 | a0012 | 1 | HG02886.hp2 | missense_variant | MODERATE | c.140G>A | p.Ser47Asn | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 2/14 | 363/9957 | 140/2727 | 47/908 | chr2 | 17760083 | ||
chr2:17761508
|
T | A | 14 | a0001a0003a0004others(11): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
missense_variant | MODERATE | c.274T>A | p.Ser92Thr | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 3/14 | 497/9957 | 274/2727 | 92/908 | chr2 | 17761508 | ||
chr2:17764938
|
G | C | 1 | a0013 | 1 | HG00735.hp1 | missense_variant | MODERATE | c.390G>C | p.Gln130His | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 4/14 | 613/9957 | 390/2727 | 130/908 | chr2 | 17764938 | ||
chr2:17764976
|
A | G | 3 | a0003a0009a0011 | 48 | HG00140.hp1 HG00639.hp1 HG01069.hp1 others(45): Show |
missense_variant | MODERATE | c.428A>G | p.Asn143Ser | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 4/14 | 651/9957 | 428/2727 | 143/908 | chr2 | 17764976 | ||
chr2:17766619
|
G | A | 1 | a0009 | 7 | HG01069.hp1 HG01070.hp2 HG01071.hp2 others(4): Show |
missense_variant | MODERATE | c.566G>A | p.Ser189Asn | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 5/14 | 789/9957 | 566/2727 | 189/908 | chr2 | 17766619 | ||
chr2:17766660
|
A | G | 2 | a0005a0006 | 29 | HG00621.hp2 HG00639.hp2 HG02257.hp2 others(26): Show |
missense_variant | MODERATE | c.607A>G | p.Ile203Val | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 5/14 | 830/9957 | 607/2727 | 203/908 | chr2 | 17766660 | ||
chr2:17772672
|
T | C | 1 | a0017 | 1 | HG03654.hp2 | missense_variant | MODERATE | c.841T>C | p.Cys281Arg | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 8/14 | 1064/9957 | 841/2727 | 281/908 | chr2 | 17772672 | ||
chr2:17772760
|
G | A | 15 | a0001a0002a0003others(12): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
missense_variant | MODERATE | c.929G>A | p.Ser310Asn | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 8/14 | 1152/9957 | 929/2727 | 310/908 | chr2 | 17772760 | ||
chr2:17773130
|
G | A | 1 | a0011 | 3 | HG03669.hp1 HG04199.hp1 HG04204.hp1 |
missense_variant&splice_region_variant | MODERATE | c.988G>A | p.Glu330Lys | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 9/14 | 1211/9957 | 988/2727 | 330/908 | chr2 | 17773130 | ||
chr2:17781251
|
C | T | 11 | a0001a0003a0004others(8): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
missense_variant | MODERATE | c.2039C>T | p.Thr680Ile | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 2262/9957 | 2039/2727 | 680/908 | chr2 | 17781251 | ||
chr2:17781647
|
A | G | 1 | a0015 | 1 | HG01069.hp2 | missense_variant | MODERATE | c.2435A>G | p.Lys812Arg | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 2658/9957 | 2435/2727 | 812/908 | chr2 | 17781647 | ||
chr2:17781661
|
A | G | 1 | a0007 | 9 | HG02559.hp2 HG02615.hp1 HG02622.hp1 others(6): Show |
missense_variant | MODERATE | c.2449A>G | p.Thr817Ala | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 2672/9957 | 2449/2727 | 817/908 | chr2 | 17781661 | ||
chr2:17781726
|
CAAGTT | C | 1 | a0004 | 30 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(27): Show |
frameshift_variant | HIGH | c.2515_2519delAAGTT | p.Lys839fs | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 2738/9957 | 2515/2727 | 839/908 | chr2 | 17781726 | ||
chr2:17781831
|
T | G | 1 | a0005 | 16 | HG00621.hp2 HG00639.hp2 NA18945.hp2 others(13): Show |
missense_variant | MODERATE | c.2619T>G | p.Ser873Arg | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 2842/9957 | 2619/2727 | 873/908 | chr2 | 17781831 | ||
chr2:17781864
|
A | C | 1 | a0014 | 1 | HG02572.hp2 | missense_variant | MODERATE | c.2652A>C | p.Glu884Asp | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 2875/9957 | 2652/2727 | 884/908 | chr2 | 17781864 | ||
chr2:17788241
|
AGCAAAGC others(5698): Show |
A | 1 | a0007 | 1 | NA20129.hp2 | splice_region_variant | LOW | c.*6303_*12007del | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | chr2 | 17788241 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:17764974
|
C | T | 1 | a0001c0020 | 1 | HG03688.hp2 | synonymous_variant | LOW | c.426C>T | p.Leu142Leu | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 4/14 | 649/9957 | 426/2727 | 142/908 | chr2 | 17764974 | ||
chr2:17780054
|
A | G | 2 | a0005c0005a0006c0006 | 29 | HG00621.hp2 HG00639.hp2 HG02257.hp2 others(26): Show |
synonymous_variant | LOW | c.1341A>G | p.Ala447Ala | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 13/14 | 1564/9957 | 1341/2727 | 447/908 | chr2 | 17780054 | ||
chr2:17780850
|
T | A | 1 | a0003c0019 | 1 | HG00140.hp1 | synonymous_variant | LOW | c.1638T>A | p.Ser546Ser | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 1861/9957 | 1638/2727 | 546/908 | chr2 | 17780850 | ||
chr2:17781183
|
A | G | 6 | a0001c0001a0001c0020a0004c0004others(3): Show | 165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
synonymous_variant | LOW | c.1971A>G | p.Glu657Glu | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 2194/9957 | 1971/2727 | 657/908 | chr2 | 17781183 | ||
chr2:17781657
|
C | T | 1 | a0009c0018 | 1 | HG01070.hp2 | synonymous_variant | LOW | c.2445C>T | p.Tyr815Tyr | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 2668/9957 | 2445/2727 | 815/908 | chr2 | 17781657 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:17754185
|
C | T | 1 | a0001c0001t0053 | 1 | NA18946.hp1 | 5_prime_UTR_variant | MODIFIER | c.-176C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/14 | 5759 | chr2 | 17754185 | |||||
chr2:17754227
|
CT | C | 9 | a0005c0005t0005a0005c0005t0008a0005c0005t0027others(6): Show | 29 | HG00621.hp2 HG00639.hp2 HG02257.hp2 others(26): Show |
5_prime_UTR_variant | MODIFIER | c.-123delT | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/14 | 5706 | INFO_REALIGN_3_PRIME | chr2 | 17754227 | ||||
chr2:17754228
|
T | C | 4 | a0003c0003t0006a0003c0003t0013a0003c0003t0024others(1): Show | 13 | HG01884.hp1 HG02056.hp2 HG02145.hp2 others(10): Show |
5_prime_UTR_variant | MODIFIER | c.-133T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/14 | 5716 | chr2 | 17754228 | |||||
chr2:17759932
|
A | G | 1 | a0003c0003t0052 | 1 | HG03516.hp1 | 5_prime_UTR_variant | MODIFIER | c.-12A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 2/14 | 12 | chr2 | 17759932 | |||||
chr2:17782044
|
C | G | 1 | a0004c0004t0023 | 2 | HG00642.hp1 HG01175.hp2 |
3_prime_UTR_variant | MODIFIER | c.*105C>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 105 | chr2 | 17782044 | |||||
chr2:17782220
|
A | G | 1 | a0011c0011t0015 | 3 | HG03669.hp1 HG04199.hp1 HG04204.hp1 |
3_prime_UTR_variant | MODIFIER | c.*281A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 281 | chr2 | 17782220 | |||||
chr2:17782526
|
C | T | 1 | a0002c0002t0022 | 2 | NA18955.hp1 NA19067.hp1 |
3_prime_UTR_variant | MODIFIER | c.*587C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 587 | chr2 | 17782526 | |||||
chr2:17783001
|
A | T | 1 | a0001c0001t0051 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1062A>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 1062 | chr2 | 17783001 | |||||
chr2:17783072
|
T | G | 10 | a0001c0001t0030a0005c0005t0005a0005c0005t0008others(7): Show | 30 | HG00621.hp2 HG00639.hp2 HG02027.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*1133T>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 1133 | chr2 | 17783072 | |||||
chr2:17783093
|
T | C | 3 | a0008c0008t0012a0008c0008t0016a0012c0013t0012 | 6 | HG01109.hp2 HG02258.hp2 HG02886.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1154T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 1154 | chr2 | 17783093 | |||||
chr2:17783099
|
C | T | 9 | a0005c0005t0005a0005c0005t0008a0005c0005t0027others(6): Show | 29 | HG00621.hp2 HG00639.hp2 HG02257.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*1160C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 1160 | chr2 | 17783099 | |||||
chr2:17783296
|
C | T | 1 | a0003c0003t0013 | 3 | NA18959.hp1 NA18967.hp2 NA18989.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1357C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 1357 | chr2 | 17783296 | |||||
chr2:17783648
|
A | G | 1 | a0003c0003t0050 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1709A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 1709 | chr2 | 17783648 | |||||
chr2:17783730
|
A | G | 6 | a0005c0005t0005a0005c0005t0008a0005c0005t0027others(3): Show | 20 | HG00621.hp2 HG00639.hp2 HG02451.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1791A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 1791 | chr2 | 17783730 | |||||
chr2:17784383
|
C | T | 1 | a0003c0003t0025 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2444C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 2444 | chr2 | 17784383 | |||||
chr2:17784432
|
C | T | 17 | a0003c0003t0003a0003c0003t0006a0003c0003t0013others(14): Show | 48 | HG00140.hp1 HG00639.hp1 HG01069.hp1 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*2493C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 2493 | chr2 | 17784432 | |||||
chr2:17784488
|
T | C | 1 | a0001c0001t0031 | 1 | NA18993.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2549T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 2549 | chr2 | 17784488 | |||||
chr2:17784522
|
G | A | 2 | a0007c0007t0032a0007c0007t0033 | 2 | HG02622.hp1 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2583G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 2583 | chr2 | 17784522 | |||||
chr2:17784553
|
A | G | 13 | a0003c0003t0003a0003c0003t0020a0003c0003t0047others(10): Show | 35 | HG00140.hp1 HG00639.hp1 HG01069.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*2614A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 2614 | chr2 | 17784553 | |||||
chr2:17784584
|
G | A | 1 | a0006c0006t0026 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2645G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 2645 | chr2 | 17784584 | |||||
chr2:17784656
|
C | G | 9 | a0005c0005t0005a0005c0005t0008a0005c0005t0027others(6): Show | 29 | HG00621.hp2 HG00639.hp2 HG02257.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*2717C>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 2717 | chr2 | 17784656 | |||||
chr2:17784664
|
G | A | 20 | a0001c0001t0001a0001c0001t0004a0001c0001t0009others(17): Show | 164 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(161): Show |
3_prime_UTR_variant | MODIFIER | c.*2725G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 2725 | chr2 | 17784664 | |||||
chr2:17784673
|
T | G | 1 | a0015c0015t0040 | 1 | HG01069.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2734T>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 2734 | chr2 | 17784673 | |||||
chr2:17784677
|
A | G | 3 | a0002c0002t0007a0002c0002t0045a0002c0002t0046 | 8 | HG00642.hp2 HG02055.hp1 HG02970.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2738A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 2738 | chr2 | 17784677 | |||||
chr2:17784691
|
CAGAG | C | 9 | a0005c0005t0005a0005c0005t0008a0005c0005t0027others(6): Show | 29 | HG00621.hp2 HG00639.hp2 HG02257.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*2756_*2759delGAGA | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 2756 | INFO_REALIGN_3_PRIME | chr2 | 17784691 | ||||
chr2:17784890
|
A | G | 49 | a0001c0001t0001a0001c0001t0004a0001c0001t0009others(46): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
3_prime_UTR_variant | MODIFIER | c.*2951A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 2951 | chr2 | 17784890 | |||||
chr2:17784934
|
G | A | 1 | a0001c0001t0034 | 1 | HG00423.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2995G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 2995 | chr2 | 17784934 | |||||
chr2:17784982
|
A | T | 2 | a0006c0006t0010a0006c0006t0011 | 8 | HG02257.hp2 HG02280.hp2 HG02630.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3043A>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 3043 | chr2 | 17784982 | |||||
chr2:17784987
|
C | T | 1 | a0003c0003t0049 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3048C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 3048 | chr2 | 17784987 | |||||
chr2:17785154
|
T | G | 49 | a0001c0001t0001a0001c0001t0004a0001c0001t0009others(46): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
3_prime_UTR_variant | MODIFIER | c.*3215T>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 3215 | chr2 | 17785154 | |||||
chr2:17785208
|
G | A | 1 | a0007c0007t0017 | 2 | HG03130.hp2 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3269G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 3269 | chr2 | 17785208 | |||||
chr2:17785226
|
A | G | 1 | a0006c0006t0011 | 4 | HG02965.hp2 HG02970.hp1 NA18906.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3287A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 3287 | chr2 | 17785226 | |||||
chr2:17785307
|
T | C | 1 | a0008c0008t0041 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3368T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 3368 | chr2 | 17785307 | |||||
chr2:17785464
|
T | C | 2 | a0005c0005t0005a0005c0005t0027 | 13 | NA18945.hp2 NA18946.hp2 NA18957.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*3525T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 3525 | chr2 | 17785464 | |||||
chr2:17785586
|
A | AT | 48 | a0001c0001t0001a0001c0001t0004a0001c0001t0009others(45): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
3_prime_UTR_variant | MODIFIER | c.*3654dupT | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 3655 | INFO_REALIGN_3_PRIME | chr2 | 17785586 | ||||
chr2:17785752
|
G | C | 1 | a0001c0001t0035 | 1 | NA18986.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3813G>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 3813 | chr2 | 17785752 | |||||
chr2:17785763
|
G | A | 1 | a0001c0012t0018 | 2 | HG02572.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3824G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 3824 | chr2 | 17785763 | |||||
chr2:17785825
|
C | T | 2 | a0002c0002t0007a0002c0002t0046 | 7 | HG02055.hp1 HG02970.hp2 HG03041.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3886C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 3886 | chr2 | 17785825 | |||||
chr2:17785839
|
A | G | 1 | a0005c0005t0027 | 1 | NA18946.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3900A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 3900 | chr2 | 17785839 | |||||
chr2:17785862
|
T | G | 3 | a0006c0006t0010a0006c0006t0011a0006c0006t0026 | 9 | HG02257.hp2 HG02280.hp2 HG02615.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3923T>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 3923 | chr2 | 17785862 | |||||
chr2:17785888
|
C | A | 1 | a0009c0009t0019 | 2 | HG03239.hp2 HG03710.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3949C>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 3949 | chr2 | 17785888 | |||||
chr2:17785900
|
A | T | 1 | a0015c0015t0040 | 1 | HG01069.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3961A>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 3961 | chr2 | 17785900 | |||||
chr2:17785919
|
A | T | 6 | a0005c0005t0005a0005c0005t0008a0005c0005t0027others(3): Show | 20 | HG00621.hp2 HG00639.hp2 HG02451.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*3980A>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 3980 | chr2 | 17785919 | |||||
chr2:17786014
|
T | G | 22 | a0001c0001t0001a0001c0001t0004a0001c0001t0009others(19): Show | 166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
3_prime_UTR_variant | MODIFIER | c.*4075T>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 4075 | chr2 | 17786014 | |||||
chr2:17786035
|
A | G | 1 | a0003c0003t0048 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4096A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 4096 | chr2 | 17786035 | |||||
chr2:17786141
|
A | G | 1 | a0004c0004t0039 | 1 | NA19010.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4202A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 4202 | chr2 | 17786141 | |||||
chr2:17786234
|
C | T | 3 | a0001c0001t0004a0001c0001t0038a0001c0001t0053 | 16 | NA18946.hp1 NA18964.hp1 NA18968.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*4295C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 4295 | chr2 | 17786234 | |||||
chr2:17786319
|
A | G | 27 | a0001c0012t0018a0003c0003t0003a0003c0003t0006others(24): Show | 79 | HG00140.hp1 HG00621.hp2 HG00639.hp1 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*4380A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 4380 | chr2 | 17786319 | |||||
chr2:17786532
|
A | G | 1 | a0002c0002t0046 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4593A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 4593 | chr2 | 17786532 | |||||
chr2:17786569
|
C | T | 18 | a0001c0012t0018a0003c0003t0003a0003c0003t0006others(15): Show | 50 | HG00140.hp1 HG00639.hp1 HG01069.hp1 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*4630C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 4630 | chr2 | 17786569 | |||||
chr2:17786583
|
A | G | 9 | a0005c0005t0005a0005c0005t0008a0005c0005t0027others(6): Show | 29 | HG00621.hp2 HG00639.hp2 HG02257.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*4644A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 4644 | chr2 | 17786583 | |||||
chr2:17786675
|
C | T | 1 | a0015c0015t0040 | 1 | HG01069.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4736C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 4736 | chr2 | 17786675 | |||||
chr2:17786803
|
G | A | 1 | a0001c0012t0018 | 2 | HG02572.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4864G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 4864 | chr2 | 17786803 | |||||
chr2:17786948
|
C | A | 17 | a0003c0003t0003a0003c0003t0006a0003c0003t0013others(14): Show | 48 | HG00140.hp1 HG00639.hp1 HG01069.hp1 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*5009C>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 5009 | chr2 | 17786948 | |||||
chr2:17787066
|
T | C | 1 | a0008c0008t0016 | 2 | HG02258.hp2 HG02922.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5127T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 5127 | chr2 | 17787066 | |||||
chr2:17787081
|
T | C | 1 | a0006c0006t0028 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5142T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 5142 | chr2 | 17787081 | |||||
chr2:17787096
|
T | G | 1 | a0008c0008t0041 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5157T>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 5157 | chr2 | 17787096 | |||||
chr2:17787237
|
C | T | 1 | a0001c0001t0009 | 5 | HG00099.hp2 HG00280.hp1 HG02055.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5298C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 5298 | chr2 | 17787237 | |||||
chr2:17787266
|
G | A | 9 | a0005c0005t0005a0005c0005t0008a0005c0005t0027others(6): Show | 29 | HG00621.hp2 HG00639.hp2 HG02257.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*5327G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 5327 | chr2 | 17787266 | |||||
chr2:17787369
|
C | A | 1 | a0002c0002t0043 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5430C>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 5430 | chr2 | 17787369 | |||||
chr2:17787378
|
G | A | 3 | a0008c0008t0012a0008c0008t0016a0012c0013t0012 | 6 | HG01109.hp2 HG02258.hp2 HG02886.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5439G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 5439 | chr2 | 17787378 | |||||
chr2:17787421
|
A | T | 1 | a0001c0012t0018 | 2 | HG02572.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5482A>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 5482 | chr2 | 17787421 | |||||
chr2:17787473
|
T | C | 1 | a0003c0003t0024 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5534T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 5534 | chr2 | 17787473 | |||||
chr2:17787559
|
A | G | 1 | a0009c0009t0021 | 2 | HG01069.hp1 HG01071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5620A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 5620 | chr2 | 17787559 | |||||
chr2:17787572
|
C | T | 1 | a0001c0001t0037 | 1 | NA18967.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5633C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 5633 | chr2 | 17787572 | |||||
chr2:17787617
|
C | T | 9 | a0005c0005t0005a0005c0005t0008a0005c0005t0027others(6): Show | 29 | HG00621.hp2 HG00639.hp2 HG02257.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*5678C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 5678 | chr2 | 17787617 | |||||
chr2:17787682
|
G | C | 2 | a0007c0007t0032a0007c0007t0033 | 2 | HG02622.hp1 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5743G>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 5743 | chr2 | 17787682 | |||||
chr2:17787746
|
A | G | 1 | a0003c0003t0020 | 2 | HG00639.hp1 HG01074.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5807A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 5807 | chr2 | 17787746 | |||||
chr2:17787757
|
C | T | 1 | a0001c0001t0038 | 1 | NA18968.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5818C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 5818 | chr2 | 17787757 | |||||
chr2:17787781
|
G | A | 9 | a0005c0005t0005a0005c0005t0008a0005c0005t0027others(6): Show | 29 | HG00621.hp2 HG00639.hp2 HG02257.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*5842G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 5842 | chr2 | 17787781 | |||||
chr2:17787848
|
C | T | 3 | a0008c0008t0012a0008c0008t0016a0012c0013t0012 | 6 | HG01109.hp2 HG02258.hp2 HG02886.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5909C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 5909 | chr2 | 17787848 | |||||
chr2:17788059
|
G | A | 1 | a0008c0008t0041 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6120G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 6120 | chr2 | 17788059 | |||||
chr2:17788078
|
C | T | 27 | a0001c0012t0018a0003c0003t0003a0003c0003t0006others(24): Show | 79 | HG00140.hp1 HG00621.hp2 HG00639.hp1 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*6139C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 6139 | chr2 | 17788078 | |||||
chr2:17788157
|
G | A | 2 | a0001c0001t0009a0001c0001t0014 | 8 | HG00099.hp2 HG00280.hp1 HG02055.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*6218G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 6218 | chr2 | 17788157 | |||||
chr2:17788193
|
C | T | 1 | a0005c0005t0029 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6254C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 6254 | chr2 | 17788193 | |||||
chr2:17788282
|
C | T | 1 | a0011c0011t0015 | 3 | HG03669.hp1 HG04199.hp1 HG04204.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6343C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 6343 | chr2 | 17788282 | |||||
chr2:17788675
|
T | A | 1 | a0003c0003t0052 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6736T>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 6736 | chr2 | 17788675 | |||||
chr2:17788753
|
G | C | 1 | a0001c0001t0036 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6814G>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 6814 | chr2 | 17788753 | |||||
chr2:17788791
|
G | A | 1 | a0007c0007t0017 | 2 | HG03130.hp2 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6852G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 6852 | chr2 | 17788791 | |||||
chr2:17788909
|
C | T | 1 | a0003c0003t0047 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6970C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 14/14 | 6970 | chr2 | 17788909 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:17754382
|
G | T | 6 | a0006c0006t0010g0018a0006c0006t0010g0214a0006c0006t0011g0044others(3): Show | 9 | HG02257.hp2 HG02280.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.-16+37G>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17754382 | ||||||
chr2:17754431
|
T | C | 1 | a0008c0008t0041g0045 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-16+86T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17754431 | ||||||
chr2:17754460
|
A | G | 1 | a0001c0001t0001g0210 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-16+115A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17754460 | ||||||
chr2:17754513
|
T | C | 112 | a0001c0012t0018g0019a0002c0002t0002g0009a0002c0002t0002g0010others(109): Show | 153 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.-16+168T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17754513 | ||||||
chr2:17754542
|
C | T | 1 | a0001c0001t0001g0209 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-16+197C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17754542 | ||||||
chr2:17754627
|
G | C | 1 | a0001c0012t0018g0019 | 2 | HG02572.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-16+282G>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17754627 | ||||||
chr2:17754629
|
G | C | 3 | a0003c0003t0003g0007a0003c0003t0003g0046a0003c0003t0003g0047 | 5 | HG01891.hp2 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-16+284G>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17754629 | ||||||
chr2:17754801
|
C | T | 1 | a0001c0012t0018g0019 | 2 | HG02572.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-16+456C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17754801 | ||||||
chr2:17754839
|
C | T | 1 | a0015c0015t0040g0121 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-16+494C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17754839 | ||||||
chr2:17754918
|
T | C | 1 | a0003c0003t0003g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-16+573T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17754918 | ||||||
chr2:17754924
|
A | T | 2 | a0001c0001t0001g0207a0001c0001t0001g0208 | 2 | HG02074.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.-16+579A>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17754924 | ||||||
chr2:17754985
|
C | T | 3 | a0003c0003t0013g0118a0003c0003t0013g0119a0003c0003t0013g0120 | 3 | NA18959.hp1 NA18967.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.-16+640C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17754985 | ||||||
chr2:17755084
|
CAA | C | 2 | a0003c0003t0003g0013a0003c0003t0020g0013 | 3 | HG00639.hp1 HG01074.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-16+741_-16+742del others(2): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 17755084 | |||||
chr2:17755312
|
G | T | 1 | a0001c0001t0001g0206 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-16+967G>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17755312 | ||||||
chr2:17755514
|
A | C | 1 | a0003c0003t0003g0117 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-16+1169A>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17755514 | ||||||
chr2:17755875
|
T | C | 1 | a0001c0012t0018g0019 | 2 | HG02572.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-16+1530T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17755875 | ||||||
chr2:17755897
|
T | G | 2 | a0002c0002t0002g0020a0002c0002t0002g0048 | 3 | HG01515.hp1 HG01517.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.-16+1552T>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17755897 | ||||||
chr2:17755980
|
A | T | 1 | a0003c0003t0024g0116 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-16+1635A>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17755980 | ||||||
chr2:17755986
|
A | G | 14 | a0005c0005t0005g0002a0005c0005t0005g0112a0005c0005t0008g0002others(11): Show | 29 | HG00621.hp2 HG00639.hp2 HG02257.hp2 others(26): Show |
intron_variant | MODIFIER | c.-16+1641A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17755986 | ||||||
chr2:17756016
|
A | G | 115 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(112): Show | 165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.-16+1671A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17756016 | ||||||
chr2:17756097
|
A | G | 1 | a0003c0003t0003g0111 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-16+1752A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17756097 | ||||||
chr2:17756122
|
G | A | 1 | a0008c0008t0041g0045 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-16+1777G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17756122 | ||||||
chr2:17756147
|
C | T | 14 | a0005c0005t0005g0002a0005c0005t0005g0112a0005c0005t0008g0002others(11): Show | 29 | HG00621.hp2 HG00639.hp2 HG02257.hp2 others(26): Show |
intron_variant | MODIFIER | c.-16+1802C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17756147 | ||||||
chr2:17756272
|
C | G | 1 | a0004c0004t0001g0205 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-16+1927C>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17756272 | ||||||
chr2:17756482
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-16+2137G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17756482 | ||||||
chr2:17756502
|
AC | A | 41 | a0003c0003t0003g0007a0003c0003t0003g0013a0003c0003t0003g0023others(38): Show | 48 | HG00140.hp1 HG00639.hp1 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.-16+2158delC | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17756502 | ||||||
chr2:17756831
|
G | A | 1 | a0001c0001t0001g0123 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-16+2486G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17756831 | ||||||
chr2:17757008
|
G | A | 1 | a0002c0002t0007g0075 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-16+2663G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17757008 | ||||||
chr2:17757147
|
C | T | 3 | a0004c0004t0001g0006a0004c0004t0001g0203a0004c0004t0001g0204 | 6 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15-2782C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17757147 | ||||||
chr2:17757234
|
A | G | 115 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(112): Show | 165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.-15-2695A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17757234 | ||||||
chr2:17757246
|
CT | C | 44 | a0001c0001t0001g0124a0001c0012t0018g0019a0003c0003t0003g0007others(41): Show | 52 | HG00140.hp1 HG00639.hp1 HG01069.hp1 others(49): Show |
intron_variant | MODIFIER | c.-15-2666delT | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 17757246 | |||||
chr2:17757387
|
A | T | 1 | a0001c0001t0014g0202 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-15-2542A>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17757387 | ||||||
chr2:17757484
|
A | G | 1 | a0008c0008t0041g0045 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-15-2445A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17757484 | ||||||
chr2:17757540
|
G | A | 1 | a0008c0008t0041g0045 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-15-2389G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17757540 | ||||||
chr2:17757644
|
A | T | 1 | a0001c0001t0001g0208 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-15-2285A>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17757644 | ||||||
chr2:17757729
|
G | C | 1 | a0007c0007t0002g0025 | 2 | HG02559.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.-15-2200G>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17757729 | ||||||
chr2:17758269
|
G | A | 25 | a0003c0003t0003g0007a0003c0003t0003g0013a0003c0003t0003g0023others(22): Show | 31 | HG00639.hp1 HG01069.hp1 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.-15-1660G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17758269 | ||||||
chr2:17758468
|
T | C | 1 | a0001c0001t0001g0125 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-15-1461T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17758468 | ||||||
chr2:17758607
|
C | T | 1 | a0001c0001t0001g0201 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-15-1322C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17758607 | ||||||
chr2:17758817
|
G | T | 8 | a0005c0005t0005g0002a0005c0005t0005g0112a0005c0005t0008g0002others(5): Show | 20 | HG00621.hp2 HG00639.hp2 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.-15-1112G>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17758817 | ||||||
chr2:17758819
|
G | A | 14 | a0005c0005t0005g0002a0005c0005t0005g0112a0005c0005t0008g0002others(11): Show | 29 | HG00621.hp2 HG00639.hp2 HG02257.hp2 others(26): Show |
intron_variant | MODIFIER | c.-15-1110G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17758819 | ||||||
chr2:17758831
|
G | A | 6 | a0002c0002t0002g0026a0002c0002t0002g0076a0002c0002t0002g0077others(3): Show | 7 | HG01891.hp1 HG02257.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-15-1098G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17758831 | ||||||
chr2:17758831
|
G | C | 28 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0014others(25): Show | 42 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(39): Show |
intron_variant | MODIFIER | c.-15-1098G>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17758831 | ||||||
chr2:17758839
|
G | A | 1 | a0003c0003t0049g0049 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-15-1090G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17758839 | ||||||
chr2:17758847
|
C | T | 7 | a0001c0001t0009g0015a0001c0001t0009g0139a0001c0001t0009g0140others(4): Show | 8 | HG00099.hp2 HG00280.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.-15-1082C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17758847 | ||||||
chr2:17758869
|
A | G | 2 | a0001c0001t0001g0043a0001c0001t0001g0200 | 3 | HG02717.hp1 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-15-1060A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17758869 | ||||||
chr2:17758899
|
A | G | 1 | a0001c0001t0001g0199 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-15-1030A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17758899 | ||||||
chr2:17759129
|
G | A | 1 | a0001c0001t0051g0143 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-15-800G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17759129 | ||||||
chr2:17759159
|
T | C | 14 | a0005c0005t0005g0002a0005c0005t0005g0112a0005c0005t0008g0002others(11): Show | 29 | HG00621.hp2 HG00639.hp2 HG02257.hp2 others(26): Show |
intron_variant | MODIFIER | c.-15-770T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17759159 | ||||||
chr2:17759386
|
A | C | 41 | a0003c0003t0003g0007a0003c0003t0003g0013a0003c0003t0003g0023others(38): Show | 48 | HG00140.hp1 HG00639.hp1 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.-15-543A>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17759386 | ||||||
chr2:17759430
|
G | A | 1 | a0004c0004t0023g0144 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-15-499G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17759430 | ||||||
chr2:17759524
|
A | T | 1 | a0008c0008t0041g0045 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-15-405A>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17759524 | ||||||
chr2:17759530
|
C | T | 14 | a0005c0005t0005g0002a0005c0005t0005g0112a0005c0005t0008g0002others(11): Show | 29 | HG00621.hp2 HG00639.hp2 HG02257.hp2 others(26): Show |
intron_variant | MODIFIER | c.-15-399C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17759530 | ||||||
chr2:17759644
|
A | C | 1 | a0001c0001t0001g0138 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-15-285A>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17759644 | ||||||
chr2:17759750
|
A | G | 1 | a0001c0001t0030g0198 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-15-179A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17759750 | ||||||
chr2:17759796
|
C | T | 1 | a0002c0002t0002g0080 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-15-133C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17759796 | ||||||
chr2:17759821
|
A | G | 1 | a0001c0012t0018g0019 | 2 | HG02572.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-15-108A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 1/13 | chr2 | 17759821 | ||||||
chr2:17760123
|
C | G | 1 | a0001c0001t0001g0197 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.161+19C>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 2/13 | chr2 | 17760123 | ||||||
chr2:17760156
|
T | G | 157 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(154): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.161+52T>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 2/13 | chr2 | 17760156 | ||||||
chr2:17760302
|
C | A | 2 | a0001c0001t0001g0043a0001c0001t0001g0200 | 3 | HG02717.hp1 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.161+198C>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 2/13 | chr2 | 17760302 | ||||||
chr2:17760307
|
A | G | 1 | a0002c0002t0002g0079 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.161+203A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 2/13 | chr2 | 17760307 | ||||||
chr2:17760386
|
A | G | 3 | a0001c0001t0001g0037a0001c0001t0001g0136a0001c0001t0001g0137 | 4 | HG02738.hp2 HG03490.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.161+282A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 2/13 | chr2 | 17760386 | ||||||
chr2:17760447
|
A | T | 1 | a0001c0001t0036g0135 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.161+343A>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 2/13 | chr2 | 17760447 | ||||||
chr2:17760629
|
T | G | 1 | a0001c0012t0018g0019 | 2 | HG02572.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.161+525T>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 2/13 | chr2 | 17760629 | ||||||
chr2:17760645
|
C | T | 6 | a0006c0006t0010g0018a0006c0006t0010g0214a0006c0006t0011g0044others(3): Show | 9 | HG02257.hp2 HG02280.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.161+541C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 2/13 | chr2 | 17760645 | ||||||
chr2:17760650
|
A | G | 184 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(181): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.161+546A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 2/13 | chr2 | 17760650 | ||||||
chr2:17760680
|
G | A | 1 | a0014c0016t0001g0145 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.161+576G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 2/13 | chr2 | 17760680 | ||||||
chr2:17760705
|
A | G | 14 | a0005c0005t0005g0002a0005c0005t0005g0112a0005c0005t0008g0002others(11): Show | 29 | HG00621.hp2 HG00639.hp2 HG02257.hp2 others(26): Show |
intron_variant | MODIFIER | c.161+601A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 2/13 | chr2 | 17760705 | ||||||
chr2:17760921
|
C | CA | 20 | a0001c0001t0001g0136a0001c0001t0001g0147a0001c0001t0001g0209others(17): Show | 23 | HG00735.hp1 HG01069.hp1 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.162-459dupA | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 17760921 | |||||
chr2:17760963
|
G | T | 17 | a0004c0004t0001g0003a0004c0004t0001g0006a0004c0004t0001g0039others(14): Show | 30 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(27): Show |
intron_variant | MODIFIER | c.162-433G>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 2/13 | chr2 | 17760963 | ||||||
chr2:17761011
|
A | G | 2 | a0001c0001t0001g0043a0001c0001t0001g0200 | 3 | HG02717.hp1 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.162-385A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 2/13 | chr2 | 17761011 | ||||||
chr2:17761037
|
C | A | 6 | a0002c0002t0002g0082a0002c0002t0007g0008a0002c0002t0007g0027others(3): Show | 9 | HG00642.hp2 HG01099.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.162-359C>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 2/13 | chr2 | 17761037 | ||||||
chr2:17761172
|
C | G | 1 | a0002c0002t0002g0102 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.162-224C>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 2/13 | chr2 | 17761172 | ||||||
chr2:17761198
|
C | G | 2 | a0002c0002t0002g0032a0002c0002t0042g0032 | 2 | HG01192.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.162-198C>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 2/13 | chr2 | 17761198 | ||||||
chr2:17761245
|
A | G | 1 | a0008c0008t0002g0101 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.162-151A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 2/13 | chr2 | 17761245 | ||||||
chr2:17761360
|
T | A | 14 | a0005c0005t0005g0002a0005c0005t0005g0112a0005c0005t0008g0002others(11): Show | 29 | HG00621.hp2 HG00639.hp2 HG02257.hp2 others(26): Show |
intron_variant | MODIFIER | c.162-36T>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 2/13 | chr2 | 17761360 | ||||||
chr2:17761372
|
G | A | 14 | a0005c0005t0005g0002a0005c0005t0005g0112a0005c0005t0008g0002others(11): Show | 29 | HG00621.hp2 HG00639.hp2 HG02257.hp2 others(26): Show |
intron_variant | MODIFIER | c.162-24G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 2/13 | chr2 | 17761372 | ||||||
chr2:17761589
|
A | G | 14 | a0005c0005t0005g0002a0005c0005t0005g0112a0005c0005t0008g0002others(11): Show | 29 | HG00621.hp2 HG00639.hp2 HG02257.hp2 others(26): Show |
splice_region_variant&intron_variant | LOW | c.348+7A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 3/13 | chr2 | 17761589 | ||||||
chr2:17761648
|
T | A | 1 | a0003c0003t0006g0065 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.348+66T>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 3/13 | chr2 | 17761648 | ||||||
chr2:17761661
|
A | T | 1 | a0002c0002t0002g0080 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.348+79A>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 3/13 | chr2 | 17761661 | ||||||
chr2:17761698
|
C | A | 14 | a0005c0005t0005g0002a0005c0005t0005g0112a0005c0005t0008g0002others(11): Show | 29 | HG00621.hp2 HG00639.hp2 HG02257.hp2 others(26): Show |
intron_variant | MODIFIER | c.348+116C>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 3/13 | chr2 | 17761698 | ||||||
chr2:17761748
|
T | C | 184 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(181): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.348+166T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 3/13 | chr2 | 17761748 | ||||||
chr2:17761779
|
T | G | 1 | a0008c0008t0041g0045 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.348+197T>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 3/13 | chr2 | 17761779 | ||||||
chr2:17761868
|
G | A | 2 | a0001c0001t0004g0150a0001c0001t0038g0149 | 2 | NA18968.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.348+286G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 3/13 | chr2 | 17761868 | ||||||
chr2:17761959
|
A | G | 1 | a0001c0001t0001g0134 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.348+377A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 3/13 | chr2 | 17761959 | ||||||
chr2:17761990
|
T | C | 41 | a0003c0003t0003g0007a0003c0003t0003g0013a0003c0003t0003g0023others(38): Show | 48 | HG00140.hp1 HG00639.hp1 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.348+408T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 3/13 | chr2 | 17761990 | ||||||
chr2:17762013
|
A | G | 3 | a0011c0011t0015g0072a0011c0011t0015g0073a0011c0011t0015g0074 | 3 | HG03669.hp1 HG04199.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.348+431A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 3/13 | chr2 | 17762013 | ||||||
chr2:17762063
|
G | A | 1 | a0001c0001t0004g0151 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.348+481G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 3/13 | chr2 | 17762063 | ||||||
chr2:17762063
|
G | C | 1 | a0001c0001t0035g0152 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.348+481G>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 3/13 | chr2 | 17762063 | ||||||
chr2:17762106
|
A | C | 14 | a0005c0005t0005g0002a0005c0005t0005g0112a0005c0005t0008g0002others(11): Show | 29 | HG00621.hp2 HG00639.hp2 HG02257.hp2 others(26): Show |
intron_variant | MODIFIER | c.348+524A>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 3/13 | chr2 | 17762106 | ||||||
chr2:17762173
|
C | CT | 11 | a0001c0001t0001g0043a0001c0001t0001g0147a0001c0001t0001g0200others(8): Show | 24 | HG00621.hp2 HG00639.hp2 HG02056.hp1 others(21): Show |
intron_variant | MODIFIER | c.348+601dupT | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 17762173 | |||||
chr2:17762203
|
G | GT | 14 | a0001c0001t0001g0188a0001c0001t0001g0190a0001c0001t0001g0191others(11): Show | 15 | HG00323.hp1 HG01109.hp2 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.348+637dupT | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 17762203 | |||||
chr2:17762203
|
G | T | 1 | a0003c0003t0003g0111 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.348+621G>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 3/13 | chr2 | 17762203 | ||||||
chr2:17762275
|
C | T | 2 | a0009c0009t0019g0051a0009c0009t0019g0052 | 2 | HG03239.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.348+693C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 3/13 | chr2 | 17762275 | ||||||
chr2:17762327
|
G | A | 3 | a0011c0011t0015g0072a0011c0011t0015g0073a0011c0011t0015g0074 | 3 | HG03669.hp1 HG04199.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.348+745G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 3/13 | chr2 | 17762327 | ||||||
chr2:17762408
|
T | C | 14 | a0005c0005t0005g0002a0005c0005t0005g0112a0005c0005t0008g0002others(11): Show | 29 | HG00621.hp2 HG00639.hp2 HG02257.hp2 others(26): Show |
intron_variant | MODIFIER | c.348+826T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 3/13 | chr2 | 17762408 | ||||||
chr2:17762466
|
T | C | 14 | a0005c0005t0005g0002a0005c0005t0005g0112a0005c0005t0008g0002others(11): Show | 29 | HG00621.hp2 HG00639.hp2 HG02257.hp2 others(26): Show |
intron_variant | MODIFIER | c.348+884T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 3/13 | chr2 | 17762466 | ||||||
chr2:17762511
|
T | C | 1 | a0003c0003t0006g0066 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.348+929T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 3/13 | chr2 | 17762511 | ||||||
chr2:17762753
|
T | C | 1 | a0015c0015t0040g0121 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.348+1171T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 3/13 | chr2 | 17762753 | ||||||
chr2:17762880
|
A | G | 1 | a0003c0003t0003g0062 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.348+1298A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 3/13 | chr2 | 17762880 | ||||||
chr2:17763016
|
C | T | 1 | a0003c0003t0003g0117 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.348+1434C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 3/13 | chr2 | 17763016 | ||||||
chr2:17763036
|
T | C | 14 | a0005c0005t0005g0002a0005c0005t0005g0112a0005c0005t0008g0002others(11): Show | 29 | HG00621.hp2 HG00639.hp2 HG02257.hp2 others(26): Show |
intron_variant | MODIFIER | c.348+1454T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 3/13 | chr2 | 17763036 | ||||||
chr2:17763059
|
C | G | 1 | a0006c0006t0008g0115 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.348+1477C>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 3/13 | chr2 | 17763059 | ||||||
chr2:17763088
|
C | G | 6 | a0003c0003t0003g0007a0003c0003t0003g0046a0003c0003t0003g0047others(3): Show | 8 | HG01261.hp1 HG01891.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.348+1506C>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 3/13 | chr2 | 17763088 | ||||||
chr2:17763313
|
A | G | 1 | a0004c0004t0001g0196 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.349-1584A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 3/13 | chr2 | 17763313 | ||||||
chr2:17763396
|
A | G | 1 | a0009c0009t0021g0022 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.349-1501A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 3/13 | chr2 | 17763396 | ||||||
chr2:17763580
|
A | T | 56 | a0001c0012t0018g0019a0003c0003t0003g0007a0003c0003t0003g0013others(53): Show | 79 | HG00140.hp1 HG00621.hp2 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.349-1317A>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 3/13 | chr2 | 17763580 | ||||||
chr2:17763932
|
T | C | 14 | a0005c0005t0005g0002a0005c0005t0005g0112a0005c0005t0008g0002others(11): Show | 29 | HG00621.hp2 HG00639.hp2 HG02257.hp2 others(26): Show |
intron_variant | MODIFIER | c.349-965T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 3/13 | chr2 | 17763932 | ||||||
chr2:17764078
|
A | G | 4 | a0002c0002t0002g0026a0002c0002t0002g0078a0002c0002t0002g0079others(1): Show | 5 | HG01891.hp1 HG02257.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.349-819A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 3/13 | chr2 | 17764078 | ||||||
chr2:17764205
|
G | A | 1 | a0002c0002t0002g0082 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.349-692G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 3/13 | chr2 | 17764205 | ||||||
chr2:17764238
|
A | C | 1 | a0001c0001t0001g0187 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.349-659A>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 3/13 | chr2 | 17764238 | ||||||
chr2:17764278
|
C | A | 1 | a0001c0001t0001g0153 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.349-619C>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 3/13 | chr2 | 17764278 | ||||||
chr2:17764493
|
T | G | 1 | a0001c0001t0001g0126 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.349-404T>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 3/13 | chr2 | 17764493 | ||||||
chr2:17764512
|
A | T | 1 | a0001c0001t0001g0186 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.349-385A>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 3/13 | chr2 | 17764512 | ||||||
chr2:17765111
|
G | A | 1 | a0001c0001t0001g0127 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.525+38G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 4/13 | chr2 | 17765111 | ||||||
chr2:17765180
|
C | T | 9 | a0003c0003t0006g0024a0003c0003t0006g0064a0003c0003t0006g0065others(6): Show | 10 | HG02056.hp2 HG02145.hp2 HG04204.hp2 others(7): Show |
intron_variant | MODIFIER | c.525+107C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 4/13 | chr2 | 17765180 | ||||||
chr2:17765243
|
T | C | 1 | a0001c0012t0018g0019 | 2 | HG02572.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.525+170T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 4/13 | chr2 | 17765243 | ||||||
chr2:17765327
|
G | A | 2 | a0011c0011t0015g0072a0011c0011t0015g0073 | 2 | HG04199.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.525+254G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 4/13 | chr2 | 17765327 | ||||||
chr2:17765556
|
G | A | 2 | a0005c0005t0005g0112a0005c0005t0027g0113 | 2 | NA18946.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.525+483G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 4/13 | chr2 | 17765556 | ||||||
chr2:17765885
|
A | C | 1 | a0001c0001t0001g0133 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.526-694A>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 4/13 | chr2 | 17765885 | ||||||
chr2:17765948
|
A | AAT | 5 | a0002c0002t0002g0080a0003c0003t0006g0067a0011c0011t0015g0072others(2): Show | 5 | HG01884.hp1 HG02622.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.526-614_526-613dup others(2): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 17765948 | |||||
chr2:17765948
|
A | AATAT | 5 | a0002c0002t0002g0009a0002c0002t0002g0020a0002c0002t0002g0048others(2): Show | 8 | HG00280.hp2 HG01168.hp1 HG01346.hp1 others(5): Show |
intron_variant | MODIFIER | c.526-616_526-613dup others(4): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 17765948 | |||||
chr2:17765948
|
AAT | A | 141 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(138): Show | 210 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.526-614_526-613del others(2): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 17765948 | |||||
chr2:17765989
|
G | A | 3 | a0002c0002t0002g0087a0002c0002t0002g0088a0002c0002t0002g0089 | 3 | HG02559.hp1 HG02723.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.526-590G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 4/13 | chr2 | 17765989 | ||||||
chr2:17766095
|
A | G | 5 | a0003c0003t0003g0023a0003c0003t0003g0057a0003c0003t0003g0059others(2): Show | 6 | HG01243.hp1 HG01884.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.526-484A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 4/13 | chr2 | 17766095 | ||||||
chr2:17766191
|
G | A | 1 | a0001c0012t0018g0019 | 2 | HG02572.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.526-388G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 4/13 | chr2 | 17766191 | ||||||
chr2:17766356
|
G | A | 41 | a0003c0003t0003g0007a0003c0003t0003g0013a0003c0003t0003g0023others(38): Show | 48 | HG00140.hp1 HG00639.hp1 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.526-223G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 4/13 | chr2 | 17766356 | ||||||
chr2:17766410
|
T | C | 1 | a0003c0019t0003g0068 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.526-169T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 4/13 | chr2 | 17766410 | ||||||
chr2:17766481
|
A | G | 14 | a0005c0005t0005g0002a0005c0005t0005g0112a0005c0005t0008g0002others(11): Show | 29 | HG00621.hp2 HG00639.hp2 HG02257.hp2 others(26): Show |
intron_variant | MODIFIER | c.526-98A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 4/13 | chr2 | 17766481 | ||||||
chr2:17766740
|
C | T | 1 | a0002c0002t0002g0020 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.636+51C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 5/13 | chr2 | 17766740 | ||||||
chr2:17766767
|
A | G | 41 | a0003c0003t0003g0007a0003c0003t0003g0013a0003c0003t0003g0023others(38): Show | 48 | HG00140.hp1 HG00639.hp1 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.636+78A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 5/13 | chr2 | 17766767 | ||||||
chr2:17766857
|
G | A | 1 | a0003c0019t0003g0068 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.636+168G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 5/13 | chr2 | 17766857 | ||||||
chr2:17766948
|
A | G | 41 | a0003c0003t0003g0007a0003c0003t0003g0013a0003c0003t0003g0023others(38): Show | 48 | HG00140.hp1 HG00639.hp1 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.636+259A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 5/13 | chr2 | 17766948 | ||||||
chr2:17767083
|
C | G | 1 | a0001c0001t0009g0142 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.636+394C>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 5/13 | chr2 | 17767083 | ||||||
chr2:17767152
|
G | A | 1 | a0015c0015t0040g0121 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.636+463G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 5/13 | chr2 | 17767152 | ||||||
chr2:17767247
|
A | G | 1 | a0008c0008t0016g0033 | 2 | HG02258.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.636+558A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 5/13 | chr2 | 17767247 | ||||||
chr2:17767382
|
T | C | 42 | a0001c0012t0018g0019a0003c0003t0003g0007a0003c0003t0003g0013others(39): Show | 50 | HG00140.hp1 HG00639.hp1 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.636+693T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 5/13 | chr2 | 17767382 | ||||||
chr2:17767449
|
G | A | 1 | a0001c0012t0018g0019 | 2 | HG02572.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.636+760G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 5/13 | chr2 | 17767449 | ||||||
chr2:17767685
|
C | T | 42 | a0001c0012t0018g0019a0003c0003t0003g0007a0003c0003t0003g0013others(39): Show | 50 | HG00140.hp1 HG00639.hp1 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.636+996C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 5/13 | chr2 | 17767685 | ||||||
chr2:17767753
|
A | G | 1 | a0001c0001t0053g0185 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.637-985A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 5/13 | chr2 | 17767753 | ||||||
chr2:17767968
|
T | A | 2 | a0011c0011t0015g0072a0011c0011t0015g0073 | 2 | HG04199.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.637-770T>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 5/13 | chr2 | 17767968 | ||||||
chr2:17768075
|
T | A | 41 | a0003c0003t0003g0007a0003c0003t0003g0013a0003c0003t0003g0023others(38): Show | 48 | HG00140.hp1 HG00639.hp1 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.637-663T>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 5/13 | chr2 | 17768075 | ||||||
chr2:17768085
|
G | A | 1 | a0001c0001t0001g0206 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.637-653G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 5/13 | chr2 | 17768085 | ||||||
chr2:17768093
|
G | T | 1 | a0001c0001t0001g0132 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.637-645G>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 5/13 | chr2 | 17768093 | ||||||
chr2:17768251
|
T | A | 3 | a0007c0007t0002g0012a0007c0007t0032g0107a0007c0007t0033g0108 | 5 | HG02615.hp1 HG02622.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.637-487T>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 5/13 | chr2 | 17768251 | ||||||
chr2:17768450
|
C | G | 1 | a0006c0006t0010g0214 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.637-288C>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 5/13 | chr2 | 17768450 | ||||||
chr2:17768666
|
G | A | 6 | a0003c0003t0052g0063a0009c0009t0003g0021a0009c0009t0019g0051others(3): Show | 8 | HG01069.hp1 HG01070.hp2 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.637-72G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 5/13 | chr2 | 17768666 | ||||||
chr2:17768669
|
C | A | 2 | a0001c0001t0001g0154a0001c0001t0001g0188 | 2 | NA18978.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.637-69C>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 5/13 | chr2 | 17768669 | ||||||
chr2:17768672
|
TTAA | T | 42 | a0001c0012t0018g0019a0003c0003t0003g0007a0003c0003t0003g0013others(39): Show | 50 | HG00140.hp1 HG00639.hp1 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.637-63_637-61delAT others(1): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 17768672 | |||||
chr2:17768845
|
A | G | 2 | a0001c0001t0004g0183a0001c0001t0004g0184 | 2 | NA19060.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.710+34A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 6/13 | chr2 | 17768845 | ||||||
chr2:17768928
|
C | T | 1 | a0001c0012t0018g0019 | 2 | HG02572.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.710+117C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 6/13 | chr2 | 17768928 | ||||||
chr2:17768934
|
T | C | 1 | a0008c0008t0016g0033 | 2 | HG02258.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.710+123T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 6/13 | chr2 | 17768934 | ||||||
chr2:17768961
|
T | G | 1 | a0002c0002t0002g0078 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.710+150T>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 6/13 | chr2 | 17768961 | ||||||
chr2:17768988
|
G | A | 4 | a0002c0002t0007g0008a0002c0002t0007g0027a0002c0002t0007g0075others(1): Show | 7 | HG02055.hp1 HG02970.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.710+177G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 6/13 | chr2 | 17768988 | ||||||
chr2:17769015
|
T | C | 41 | a0003c0003t0003g0007a0003c0003t0003g0013a0003c0003t0003g0023others(38): Show | 48 | HG00140.hp1 HG00639.hp1 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.710+204T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 6/13 | chr2 | 17769015 | ||||||
chr2:17769080
|
C | T | 3 | a0011c0011t0015g0072a0011c0011t0015g0073a0011c0011t0015g0074 | 3 | HG03669.hp1 HG04199.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.710+269C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 6/13 | chr2 | 17769080 | ||||||
chr2:17769553
|
T | C | 6 | a0003c0003t0052g0063a0009c0009t0003g0021a0009c0009t0019g0051others(3): Show | 8 | HG01069.hp1 HG01070.hp2 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.710+742T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 6/13 | chr2 | 17769553 | ||||||
chr2:17769584
|
C | T | 4 | a0008c0008t0012g0104a0008c0008t0012g0105a0008c0008t0012g0106others(1): Show | 4 | HG01109.hp2 HG02886.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.710+773C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 6/13 | chr2 | 17769584 | ||||||
chr2:17769812
|
TTAA | T | 14 | a0005c0005t0005g0002a0005c0005t0005g0112a0005c0005t0008g0002others(11): Show | 29 | HG00621.hp2 HG00639.hp2 HG02257.hp2 others(26): Show |
intron_variant | MODIFIER | c.710+1003_710+1005d others(5): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | 17769812 | |||||
chr2:17769893
|
C | T | 1 | a0011c0011t0015g0074 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.710+1082C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 6/13 | chr2 | 17769893 | ||||||
chr2:17770125
|
A | G | 1 | a0001c0001t0001g0182 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.711-1071A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 6/13 | chr2 | 17770125 | ||||||
chr2:17770161
|
G | A | 1 | a0003c0003t0024g0116 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.711-1035G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 6/13 | chr2 | 17770161 | ||||||
chr2:17770173
|
T | A | 1 | a0004c0004t0001g0039 | 2 | HG01106.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.711-1023T>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 6/13 | chr2 | 17770173 | ||||||
chr2:17770590
|
G | C | 1 | a0002c0002t0002g0087 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.711-606G>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 6/13 | chr2 | 17770590 | ||||||
chr2:17770660
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.711-536G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 6/13 | chr2 | 17770660 | ||||||
chr2:17770794
|
T | C | 1 | a0001c0001t0001g0187 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.711-402T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 6/13 | chr2 | 17770794 | ||||||
chr2:17770877
|
C | CA | 45 | a0003c0003t0003g0007a0003c0003t0003g0013a0003c0003t0003g0023others(42): Show | 52 | HG00140.hp1 HG00639.hp1 HG01069.hp1 others(49): Show |
intron_variant | MODIFIER | c.711-309dupA | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | 17770877 | |||||
chr2:17770897
|
G | A | 5 | a0005c0005t0005g0002a0005c0005t0005g0112a0005c0005t0008g0002others(2): Show | 16 | HG00621.hp2 HG00639.hp2 NA18945.hp2 others(13): Show |
intron_variant | MODIFIER | c.711-299G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 6/13 | chr2 | 17770897 | ||||||
chr2:17770957
|
A | G | 1 | a0015c0015t0040g0121 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.711-239A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 6/13 | chr2 | 17770957 | ||||||
chr2:17771098
|
G | A | 1 | a0008c0008t0016g0033 | 2 | HG02258.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.711-98G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 6/13 | chr2 | 17771098 | ||||||
chr2:17771175
|
A | T | 1 | a0001c0001t0001g0181 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.711-21A>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 6/13 | chr2 | 17771175 | ||||||
chr2:17771308
|
G | T | 1 | a0001c0012t0018g0019 | 2 | HG02572.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.802+21G>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 7/13 | chr2 | 17771308 | ||||||
chr2:17771511
|
G | C | 2 | a0006c0006t0011g0044a0006c0006t0011g0211 | 3 | HG02965.hp2 HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.802+224G>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 7/13 | chr2 | 17771511 | ||||||
chr2:17771691
|
A | T | 1 | a0004c0004t0001g0039 | 2 | HG01106.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.802+404A>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 7/13 | chr2 | 17771691 | ||||||
chr2:17771766
|
A | C | 3 | a0007c0007t0002g0012a0007c0007t0032g0107a0007c0007t0033g0108 | 5 | HG02615.hp1 HG02622.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.802+479A>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 7/13 | chr2 | 17771766 | ||||||
chr2:17771788
|
T | TA | 127 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(124): Show | 178 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.802+513dupA | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr2 | 17771788 | |||||
chr2:17771815
|
C | T | 1 | a0015c0015t0040g0121 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.802+528C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 7/13 | chr2 | 17771815 | ||||||
chr2:17772244
|
A | G | 5 | a0005c0005t0005g0002a0005c0005t0005g0112a0005c0005t0008g0002others(2): Show | 16 | HG00621.hp2 HG00639.hp2 NA18945.hp2 others(13): Show |
intron_variant | MODIFIER | c.803-390A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 7/13 | chr2 | 17772244 | ||||||
chr2:17772293
|
C | T | 171 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(168): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.803-341C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 7/13 | chr2 | 17772293 | ||||||
chr2:17772352
|
G | A | 1 | a0004c0004t0001g0192 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.803-282G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 7/13 | chr2 | 17772352 | ||||||
chr2:17772381
|
A | T | 28 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0014others(25): Show | 42 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(39): Show |
intron_variant | MODIFIER | c.803-253A>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 7/13 | chr2 | 17772381 | ||||||
chr2:17772583
|
A | G | 8 | a0003c0003t0003g0055a0003c0003t0049g0049a0003c0003t0052g0063others(5): Show | 10 | HG01069.hp1 HG01070.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.803-51A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 7/13 | chr2 | 17772583 | ||||||
chr2:17772873
|
A | G | 178 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(175): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.953+89A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 8/13 | chr2 | 17772873 | ||||||
chr2:17772978
|
CTGTT | C | 5 | a0003c0003t0003g0023a0003c0003t0003g0057a0003c0003t0003g0059others(2): Show | 6 | HG01243.hp1 HG01884.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.954-115_954-112del others(4): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 17772978 | |||||
chr2:17772986
|
G | A | 1 | a0007c0007t0017g0109 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.954-110G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 8/13 | chr2 | 17772986 | ||||||
chr2:17773017
|
G | A | 2 | a0002c0002t0002g0090a0002c0002t0002g0091 | 2 | HG00140.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.954-79G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 8/13 | chr2 | 17773017 | ||||||
chr2:17773154
|
C | G | 184 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(181): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.990+22C>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 9/13 | chr2 | 17773154 | ||||||
chr2:17773359
|
G | A | 1 | a0007c0007t0002g0025 | 2 | HG02559.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1071+60G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 10/13 | chr2 | 17773359 | ||||||
chr2:17773380
|
T | G | 172 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(169): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.1071+81T>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 10/13 | chr2 | 17773380 | ||||||
chr2:17773625
|
C | A | 8 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(5): Show | 8 | NA18612.hp1 NA18952.hp1 NA18971.hp1 others(5): Show |
intron_variant | MODIFIER | c.1071+326C>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 10/13 | chr2 | 17773625 | ||||||
chr2:17773673
|
G | A | 1 | a0006c0006t0026g0212 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1071+374G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 10/13 | chr2 | 17773673 | ||||||
chr2:17773937
|
T | C | 9 | a0003c0003t0003g0055a0003c0003t0003g0062a0003c0003t0049g0049others(6): Show | 11 | HG01069.hp1 HG01070.hp2 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.1072-334T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 10/13 | chr2 | 17773937 | ||||||
chr2:17773985
|
G | A | 12 | a0003c0003t0006g0024a0003c0003t0006g0064a0003c0003t0006g0065others(9): Show | 13 | HG01884.hp1 HG02056.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1072-286G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 10/13 | chr2 | 17773985 | ||||||
chr2:17773988
|
G | A | 56 | a0001c0012t0018g0019a0003c0003t0003g0007a0003c0003t0003g0013others(53): Show | 79 | HG00140.hp1 HG00621.hp2 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.1072-283G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 10/13 | chr2 | 17773988 | ||||||
chr2:17774037
|
G | A | 41 | a0003c0003t0003g0007a0003c0003t0003g0013a0003c0003t0003g0023others(38): Show | 48 | HG00140.hp1 HG00639.hp1 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.1072-234G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 10/13 | chr2 | 17774037 | ||||||
chr2:17774060
|
A | C | 1 | a0001c0001t0001g0160 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1072-211A>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 10/13 | chr2 | 17774060 | ||||||
chr2:17774216
|
G | A | 1 | a0003c0003t0003g0062 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1072-55G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 10/13 | chr2 | 17774216 | ||||||
chr2:17774231
|
G | A | 2 | a0003c0003t0013g0118a0003c0003t0013g0120 | 2 | NA18959.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.1072-40G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 10/13 | chr2 | 17774231 | ||||||
chr2:17774427
|
G | A | 6 | a0002c0002t0002g0082a0002c0002t0007g0008a0002c0002t0007g0027others(3): Show | 9 | HG00642.hp2 HG01099.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1202+26G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 11/13 | chr2 | 17774427 | ||||||
chr2:17774676
|
G | T | 1 | a0004c0004t0001g0195 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1202+275G>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 11/13 | chr2 | 17774676 | ||||||
chr2:17774690
|
G | A | 2 | a0004c0004t0023g0144a0004c0004t0023g0148 | 2 | HG00642.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.1202+289G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 11/13 | chr2 | 17774690 | ||||||
chr2:17774690
|
G | T | 1 | a0002c0002t0002g0020 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1202+289G>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 11/13 | chr2 | 17774690 | ||||||
chr2:17775061
|
C | T | 14 | a0005c0005t0005g0002a0005c0005t0005g0112a0005c0005t0008g0002others(11): Show | 29 | HG00621.hp2 HG00639.hp2 HG02257.hp2 others(26): Show |
intron_variant | MODIFIER | c.1202+660C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 11/13 | chr2 | 17775061 | ||||||
chr2:17775063
|
T | A | 1 | a0002c0002t0002g0076 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1202+662T>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 11/13 | chr2 | 17775063 | ||||||
chr2:17775078
|
G | A | 4 | a0008c0008t0012g0104a0008c0008t0012g0105a0008c0008t0012g0106others(1): Show | 4 | HG01109.hp2 HG02886.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1202+677G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 11/13 | chr2 | 17775078 | ||||||
chr2:17775225
|
A | G | 1 | a0004c0004t0001g0194 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1202+824A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 11/13 | chr2 | 17775225 | ||||||
chr2:17775439
|
A | G | 1 | a0001c0001t0001g0127 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1202+1038A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 11/13 | chr2 | 17775439 | ||||||
chr2:17775523
|
A | G | 8 | a0005c0005t0005g0002a0005c0005t0005g0112a0005c0005t0008g0002others(5): Show | 20 | HG00621.hp2 HG00639.hp2 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.1202+1122A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 11/13 | chr2 | 17775523 | ||||||
chr2:17775615
|
A | G | 1 | a0001c0001t0001g0125 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1202+1214A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 11/13 | chr2 | 17775615 | ||||||
chr2:17775686
|
G | A | 1 | a0001c0001t0001g0161 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1202+1285G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 11/13 | chr2 | 17775686 | ||||||
chr2:17775905
|
G | A | 14 | a0005c0005t0005g0002a0005c0005t0005g0112a0005c0005t0008g0002others(11): Show | 29 | HG00621.hp2 HG00639.hp2 HG02257.hp2 others(26): Show |
intron_variant | MODIFIER | c.1202+1504G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 11/13 | chr2 | 17775905 | ||||||
chr2:17775977
|
G | A | 1 | a0003c0003t0006g0065 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1202+1576G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 11/13 | chr2 | 17775977 | ||||||
chr2:17776084
|
C | T | 1 | a0003c0003t0003g0055 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1202+1683C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 11/13 | chr2 | 17776084 | ||||||
chr2:17776095
|
G | A | 1 | a0015c0015t0040g0121 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1202+1694G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 11/13 | chr2 | 17776095 | ||||||
chr2:17776115
|
C | CA | 13 | a0001c0001t0009g0142a0003c0003t0006g0065a0007c0007t0002g0012others(10): Show | 17 | HG01109.hp2 HG02258.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.1202+1735dupA | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr2 | 17776115 | |||||
chr2:17776115
|
CA | C | 128 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(125): Show | 173 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.1202+1735delA | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr2 | 17776115 | |||||
chr2:17776115
|
CAA | C | 5 | a0001c0001t0001g0180a0003c0003t0003g0013a0003c0003t0013g0118others(2): Show | 6 | HG00639.hp1 HG01070.hp2 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.1202+1734_1202+173 others(6): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr2 | 17776115 | |||||
chr2:17776199
|
C | T | 1 | a0001c0001t0001g0127 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1202+1798C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 11/13 | chr2 | 17776199 | ||||||
chr2:17776653
|
G | A | 56 | a0001c0012t0018g0019a0003c0003t0003g0007a0003c0003t0003g0013others(53): Show | 79 | HG00140.hp1 HG00621.hp2 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.1203-1349G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 11/13 | chr2 | 17776653 | ||||||
chr2:17776670
|
A | G | 3 | a0011c0011t0015g0072a0011c0011t0015g0073a0011c0011t0015g0074 | 3 | HG03669.hp1 HG04199.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1203-1332A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 11/13 | chr2 | 17776670 | ||||||
chr2:17776676
|
C | T | 3 | a0001c0001t0001g0037a0001c0001t0001g0136a0001c0001t0001g0137 | 4 | HG02738.hp2 HG03490.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.1203-1326C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 11/13 | chr2 | 17776676 | ||||||
chr2:17776853
|
C | T | 1 | a0001c0001t0001g0179 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1203-1149C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 11/13 | chr2 | 17776853 | ||||||
chr2:17776919
|
A | T | 41 | a0003c0003t0003g0007a0003c0003t0003g0013a0003c0003t0003g0023others(38): Show | 48 | HG00140.hp1 HG00639.hp1 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.1203-1083A>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 11/13 | chr2 | 17776919 | ||||||
chr2:17776994
|
T | C | 177 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(174): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.1203-1008T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 11/13 | chr2 | 17776994 | ||||||
chr2:17777327
|
A | G | 2 | a0001c0001t0001g0017a0001c0001t0001g0186 | 4 | HG02155.hp1 NA18944.hp2 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.1203-675A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 11/13 | chr2 | 17777327 | ||||||
chr2:17777435
|
A | G | 1 | a0001c0001t0001g0178 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1203-567A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 11/13 | chr2 | 17777435 | ||||||
chr2:17777495
|
G | A | 87 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(84): Show | 123 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.1203-507G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 11/13 | chr2 | 17777495 | ||||||
chr2:17777657
|
A | C | 1 | a0001c0012t0018g0019 | 2 | HG02572.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1203-345A>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 11/13 | chr2 | 17777657 | ||||||
chr2:17777720
|
C | T | 1 | a0002c0002t0002g0020 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1203-282C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 11/13 | chr2 | 17777720 | ||||||
chr2:17777746
|
C | A | 1 | a0002c0002t0002g0092 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1203-256C>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 11/13 | chr2 | 17777746 | ||||||
chr2:17777832
|
T | G | 115 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(112): Show | 165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.1203-170T>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 11/13 | chr2 | 17777832 | ||||||
chr2:17778138
|
G | GTA | 36 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0020others(33): Show | 47 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.1264+90_1264+91dup others(2): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778138 | |||||
chr2:17778138
|
GTA | G | 18 | a0001c0001t0001g0163a0001c0012t0018g0019a0003c0003t0006g0024others(15): Show | 20 | HG00140.hp1 HG01884.hp1 HG02015.hp2 others(17): Show |
intron_variant | MODIFIER | c.1264+90_1264+91del others(2): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778138 | |||||
chr2:17778140
|
A | G | 1 | a0001c0001t0001g0154 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1264+77A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778140 | ||||||
chr2:17778153
|
T | TAC | 9 | a0002c0002t0002g0011a0002c0002t0002g0030a0002c0002t0002g0090others(6): Show | 15 | HG00735.hp1 HG01109.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.1264+100_1264+101d others(4): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778153 | |||||
chr2:17778153
|
TAC | T | 116 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(113): Show | 168 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.1264+100_1264+101d others(4): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778153 | |||||
chr2:17778155
|
C | T | 4 | a0001c0001t0001g0133a0001c0001t0001g0153a0001c0001t0001g0161others(1): Show | 5 | HG02258.hp2 HG02698.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1264+92C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778155 | ||||||
chr2:17778174
|
GTA | G | 23 | a0001c0001t0001g0177a0001c0012t0018g0019a0002c0002t0022g0031others(20): Show | 40 | HG00423.hp1 HG00621.hp2 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.1264+124_1264+125d others(4): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778174 | |||||
chr2:17778174
|
GTATA | G | 3 | a0001c0001t0001g0182a0001c0001t0004g0183a0001c0001t0051g0143 | 3 | HG01243.hp2 NA18997.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.1264+122_1264+125d others(6): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778174 | |||||
chr2:17778176
|
A | G | 28 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0014others(25): Show | 42 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(39): Show |
intron_variant | MODIFIER | c.1264+113A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778176 | ||||||
chr2:17778185
|
TATAC | T | 81 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(78): Show | 117 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.1264+124_1264+127d others(6): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778185 | |||||
chr2:17778187
|
T | C | 6 | a0002c0002t0002g0026a0002c0002t0002g0076a0002c0002t0002g0077others(3): Show | 7 | HG01891.hp1 HG02257.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1264+124T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778187 | ||||||
chr2:17778187
|
TAC | T | 5 | a0002c0002t0002g0097a0008c0008t0012g0104a0008c0008t0012g0105others(2): Show | 5 | HG01109.hp1 HG01109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1264+134_1264+135d others(4): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778187 | |||||
chr2:17778189
|
C | T | 2 | a0003c0003t0024g0116a0003c0003t0049g0049 | 2 | HG01496.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1264+126C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778189 | ||||||
chr2:17778197
|
C | T | 1 | a0001c0001t0001g0177 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1264+134C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778197 | ||||||
chr2:17778197
|
CAT | C | 30 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0014others(27): Show | 44 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(41): Show |
intron_variant | MODIFIER | c.1264+139_1264+140d others(4): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778197 | |||||
chr2:17778199
|
T | C | 90 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(87): Show | 129 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.1264+136T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778199 | ||||||
chr2:17778199
|
T | G | 1 | a0001c0001t0001g0177 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1264+136T>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778199 | ||||||
chr2:17778200
|
A | G | 1 | a0001c0001t0001g0176 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1264+137A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778200 | ||||||
chr2:17778202
|
A | G | 5 | a0002c0002t0002g0076a0002c0002t0007g0008a0002c0002t0007g0027others(2): Show | 8 | HG02055.hp1 HG02280.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.1264+139A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778202 | ||||||
chr2:17778204
|
G | A | 1 | a0003c0003t0024g0116 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1264+141G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778204 | ||||||
chr2:17778206
|
GTA | G | 41 | a0001c0012t0018g0019a0003c0003t0003g0007a0003c0003t0003g0013others(38): Show | 49 | HG00140.hp1 HG00639.hp1 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.1264+151_1264+152d others(4): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778206 | |||||
chr2:17778208
|
A | G | 4 | a0001c0001t0014g0141a0003c0003t0024g0116a0003c0003t0025g0071others(1): Show | 4 | HG00423.hp1 HG04204.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1264+145A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778208 | ||||||
chr2:17778209
|
T | C | 1 | a0002c0002t0002g0076 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1264+146T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778209 | ||||||
chr2:17778212
|
ATATG | A | 2 | a0002c0002t0007g0027a0002c0002t0046g0083 | 3 | HG03041.hp2 HG03209.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1264+153_1264+156d others(6): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778212 | |||||
chr2:17778216
|
G | A | 1 | a0003c0003t0049g0049 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1264+153G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778216 | ||||||
chr2:17778219
|
T | C | 1 | a0003c0003t0049g0049 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1264+156T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778219 | ||||||
chr2:17778219
|
TAC | T | 66 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(63): Show | 88 | HG00099.hp1 HG00423.hp2 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.1264+164_1264+165d others(4): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778219 | |||||
chr2:17778221
|
C | T | 1 | a0002c0002t0002g0076 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1264+158C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778221 | ||||||
chr2:17778227
|
CAT | C | 4 | a0002c0002t0002g0011a0002c0002t0002g0082a0006c0006t0011g0213others(1): Show | 6 | HG00735.hp1 HG01099.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.1264+169_1264+170d others(4): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778227 | |||||
chr2:17778229
|
T | C | 1 | a0002c0002t0002g0076 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1264+166T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778229 | ||||||
chr2:17778229
|
T | TATATGTG others(21): Show |
4 | a0008c0008t0012g0104a0008c0008t0012g0105a0008c0008t0012g0106others(1): Show | 4 | HG01109.hp2 HG02886.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1264+190_1264+217d others(30): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778229 | |||||
chr2:17778232
|
A | G | 1 | a0002c0002t0002g0076 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1264+169A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778232 | ||||||
chr2:17778248
|
GTATACAC others(23): Show |
G | 1 | a0001c0001t0031g0158 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1264+196_1264+225d others(32): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778248 | |||||
chr2:17778248
|
GTATACAC others(111): Show |
G | 1 | a0003c0003t0003g0047 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1264+196_1264+313d others(2): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778248 | |||||
chr2:17778248
|
GTATACAC others(177): Show |
G | 1 | a0003c0003t0047g0054 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1264+196_1264+379d others(2): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778248 | |||||
chr2:17778251
|
T | C | 1 | a0001c0012t0018g0019 | 2 | HG02572.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1264+188T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778251 | ||||||
chr2:17778251
|
T | TAC | 14 | a0005c0005t0005g0002a0005c0005t0005g0112a0005c0005t0008g0002others(11): Show | 29 | HG00621.hp2 HG00639.hp2 HG02257.hp2 others(26): Show |
intron_variant | MODIFIER | c.1264+194_1264+195d others(4): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778251 | |||||
chr2:17778251
|
T | TACAC | 4 | a0001c0001t0001g0186a0002c0002t0007g0027a0002c0002t0046g0083others(1): Show | 5 | HG01069.hp2 HG03041.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1264+192_1264+195d others(6): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778251 | |||||
chr2:17778253
|
C | T | 1 | a0002c0002t0002g0076 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1264+190C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778253 | ||||||
chr2:17778253
|
CACACATA others(21): Show |
C | 3 | a0001c0001t0001g0038a0001c0001t0001g0127a0001c0001t0001g0130 | 4 | HG02027.hp2 NA18942.hp2 NA18948.hp2 others(1): Show |
intron_variant | MODIFIER | c.1264+196_1264+223d others(30): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778253 | |||||
chr2:17778255
|
CACATATG others(77): Show |
C | 5 | a0003c0003t0003g0007a0003c0003t0003g0046a0003c0003t0003g0060others(2): Show | 7 | HG01261.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1264+196_1264+279d others(86): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778255 | |||||
chr2:17778257
|
C | CACAT | 132 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(129): Show | 185 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.1264+195_1264+196i others(6): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778257 | |||||
chr2:17778257
|
C | T | 1 | a0001c0001t0036g0135 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1264+194C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778257 | ||||||
chr2:17778257
|
CATATGTG others(3): Show |
C | 1 | a0001c0001t0038g0149 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1264+196_1264+205d others(12): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778257 | |||||
chr2:17778258
|
A | ACG | 8 | a0001c0001t0001g0037a0001c0001t0001g0154a0001c0001t0001g0155others(5): Show | 9 | HG03490.hp1 HG03492.hp2 NA18612.hp1 others(6): Show |
intron_variant | MODIFIER | c.1264+195_1264+196i others(4): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778258 | ||||||
chr2:17778259
|
T | C | 3 | a0001c0001t0001g0168a0002c0002t0002g0076a0003c0019t0003g0068 | 3 | HG00140.hp1 HG02280.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.1264+196T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778259 | ||||||
chr2:17778260
|
A | ATGTGTGT others(25): Show |
1 | a0010c0010t0002g0094 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1264+217_1264+218i others(34): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778260 | |||||
chr2:17778260
|
A | ATGTGTGT others(25): Show |
2 | a0010c0010t0002g0028a0010c0010t0002g0096 | 3 | HG02717.hp2 HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1264+228_1264+259d others(34): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778260 | |||||
chr2:17778260
|
A | G | 11 | a0001c0001t0001g0037a0001c0001t0001g0154a0001c0001t0001g0155others(8): Show | 13 | HG01069.hp2 HG03041.hp2 HG03209.hp1 others(10): Show |
intron_variant | MODIFIER | c.1264+197A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778260 | ||||||
chr2:17778261
|
T | C | 1 | a0002c0002t0002g0076 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1264+198T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778261 | ||||||
chr2:17778262
|
G | A | 3 | a0001c0001t0001g0168a0002c0002t0002g0076a0003c0019t0003g0068 | 3 | HG00140.hp1 HG02280.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.1264+199G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778262 | ||||||
chr2:17778263
|
T | C | 1 | a0002c0002t0002g0011 | 3 | HG01433.hp2 HG01516.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.1264+200T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778263 | ||||||
chr2:17778264
|
G | A | 1 | a0001c0001t0001g0168 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1264+201G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778264 | ||||||
chr2:17778264
|
GTGTACAT others(77): Show |
G | 1 | a0003c0019t0003g0068 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1264+205_1264+288d others(86): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778264 | |||||
chr2:17778267
|
TACATATA others(49): Show |
T | 1 | a0001c0001t0001g0168 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1264+205_1264+260d others(58): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778267 | ||||||
chr2:17778276
|
GTA | G | 103 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 152 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.1264+218_1264+219d others(4): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778276 | |||||
chr2:17778279
|
TATACACA others(87): Show |
T | 14 | a0005c0005t0005g0002a0005c0005t0005g0112a0005c0005t0008g0002others(11): Show | 29 | HG00621.hp2 HG00639.hp2 HG02257.hp2 others(26): Show |
intron_variant | MODIFIER | c.1264+218_1264+311d others(96): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778279 | |||||
chr2:17778281
|
T | C | 42 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0161others(39): Show | 47 | HG00408.hp2 HG00639.hp1 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.1264+218T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778281 | ||||||
chr2:17778288
|
ACATG | A | 3 | a0001c0001t0004g0183a0001c0001t0004g0184a0001c0001t0051g0143 | 3 | NA18997.hp1 NA19060.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.1264+226_1264+229d others(6): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778288 | ||||||
chr2:17778289
|
C | T | 39 | a0001c0001t0001g0038a0001c0001t0001g0127a0001c0001t0001g0129others(36): Show | 45 | HG00408.hp2 HG00639.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.1264+226C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778289 | ||||||
chr2:17778290
|
A | G | 95 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(92): Show | 143 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.1264+227A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778290 | ||||||
chr2:17778291
|
T | C | 2 | a0001c0001t0001g0156a0001c0001t0001g0159 | 2 | NA18612.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.1264+228T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778291 | ||||||
chr2:17778292
|
G | A | 33 | a0001c0001t0001g0038a0001c0001t0001g0127a0001c0001t0001g0129others(30): Show | 40 | HG00408.hp2 HG00639.hp1 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.1264+229G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778292 | ||||||
chr2:17778295
|
TGTGTACA others(21): Show |
T | 3 | a0001c0001t0014g0202a0001c0001t0037g0189a0004c0004t0001g0192 | 3 | NA18952.hp2 NA18967.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1264+250_1264+277d others(30): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778295 | |||||
chr2:17778297
|
TGTACATA others(19): Show |
T | 2 | a0001c0001t0001g0043a0001c0001t0001g0200 | 3 | HG02717.hp1 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1264+237_1264+262d others(28): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778297 | |||||
chr2:17778300
|
ACATATAT others(17): Show |
A | 2 | a0001c0001t0001g0161a0001c0001t0004g0167 | 2 | HG02698.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1264+238_1264+261d others(26): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778300 | ||||||
chr2:17778308
|
GTA | G | 73 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(70): Show | 116 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.1264+250_1264+251d others(4): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778308 | |||||
chr2:17778308
|
GTATATAC others(53): Show |
G | 12 | a0003c0003t0006g0024a0003c0003t0006g0064a0003c0003t0006g0065others(9): Show | 13 | HG01884.hp1 HG02056.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1264+248_1264+307d others(62): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778308 | |||||
chr2:17778310
|
ATATACAC others(19): Show |
A | 2 | a0001c0001t0001g0133a0015c0015t0040g0121 | 2 | HG01069.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.1264+260_1264+285d others(28): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778310 | |||||
chr2:17778311
|
TATAC | T | 2 | a0001c0001t0001g0016a0001c0001t0001g0122 | 4 | HG01993.hp1 HG01993.hp2 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.1264+250_1264+253d others(6): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778311 | |||||
chr2:17778311
|
TATACACA others(53): Show |
T | 1 | a0003c0003t0003g0057 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1264+250_1264+309d others(62): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778311 | |||||
chr2:17778312
|
A | G | 1 | a0007c0007t0017g0110 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1264+249A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778312 | ||||||
chr2:17778313
|
T | C | 39 | a0001c0001t0001g0014a0001c0001t0001g0035a0001c0001t0001g0038others(36): Show | 46 | HG00408.hp2 HG00741.hp2 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.1264+250T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778313 | ||||||
chr2:17778313
|
TAC | T | 26 | a0002c0002t0002g0010a0002c0002t0002g0011a0002c0002t0002g0029others(23): Show | 35 | HG00140.hp2 HG00323.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.1264+259_1264+260d others(4): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778313 | |||||
chr2:17778313
|
TACACACA others(21): Show |
T | 6 | a0001c0001t0001g0154a0001c0001t0001g0157a0001c0001t0001g0159others(3): Show | 6 | NA18612.hp1 NA18952.hp1 NA18968.hp1 others(3): Show |
intron_variant | MODIFIER | c.1264+258_1264+285d others(30): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778313 | |||||
chr2:17778317
|
CACACACG others(7): Show |
C | 2 | a0003c0003t0048g0056a0009c0018t0003g0050 | 2 | HG01070.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.1264+256_1264+269d others(16): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778317 | |||||
chr2:17778319
|
C | CGT | 7 | a0001c0001t0001g0035a0001c0001t0001g0126a0001c0001t0001g0129others(4): Show | 8 | HG00408.hp2 HG01070.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1264+256_1264+257i others(4): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778319 | ||||||
chr2:17778319
|
C | T | 5 | a0003c0003t0003g0023a0003c0003t0003g0059a0003c0003t0003g0117others(2): Show | 6 | HG01243.hp1 HG01496.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1264+256C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778319 | ||||||
chr2:17778319
|
CACACGTG others(5): Show |
C | 9 | a0003c0003t0003g0055a0003c0003t0052g0063a0009c0009t0003g0021others(6): Show | 11 | HG01069.hp1 HG01071.hp2 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.1264+258_1264+269d others(14): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778319 | |||||
chr2:17778319
|
CACACGTG others(53): Show |
C | 2 | a0001c0001t0001g0175a0001c0001t0001g0178 | 2 | NA19006.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.1264+258_1264+317d others(62): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778319 | |||||
chr2:17778320
|
A | ATG | 6 | a0001c0001t0001g0128a0001c0001t0036g0135a0003c0003t0003g0023others(3): Show | 7 | HG01243.hp1 HG02451.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.1264+257_1264+258i others(4): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778320 | ||||||
chr2:17778320
|
A | G | 13 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0126others(10): Show | 15 | HG00408.hp2 HG01070.hp1 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.1264+257A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778320 | ||||||
chr2:17778321
|
C | CGT | 1 | a0001c0001t0001g0014 | 3 | HG00741.hp2 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1264+258_1264+259i others(4): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778321 | ||||||
chr2:17778321
|
C | T | 25 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0126others(22): Show | 28 | HG00408.hp2 HG01070.hp1 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.1264+258C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778321 | ||||||
chr2:17778321
|
CACGTGTA others(3): Show |
C | 3 | a0001c0012t0018g0019a0003c0003t0003g0013a0003c0003t0020g0013 | 5 | HG00639.hp1 HG01074.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1264+260_1264+269d others(12): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778321 | |||||
chr2:17778322
|
A | ATG | 5 | a0001c0001t0004g0183a0001c0001t0004g0184a0001c0001t0051g0143others(2): Show | 6 | HG01496.hp1 HG02258.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1264+259_1264+260i others(4): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778322 | ||||||
chr2:17778322
|
A | G | 25 | a0001c0001t0001g0014a0001c0001t0001g0035a0001c0001t0001g0038others(22): Show | 30 | HG00408.hp2 HG00741.hp2 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.1264+259A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778322 | ||||||
chr2:17778323
|
C | T | 126 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(123): Show | 182 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.1264+260C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778323 | ||||||
chr2:17778324
|
GTGTACAT others(17): Show |
G | 75 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(72): Show | 118 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.1264+265_1264+288d others(26): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778324 | |||||
chr2:17778326
|
GTACATAT others(15): Show |
G | 2 | a0001c0001t0001g0016a0001c0001t0001g0122 | 4 | HG01993.hp1 HG01993.hp2 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.1264+265_1264+286d others(24): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778326 | |||||
chr2:17778336
|
GTATACAC others(5): Show |
G | 15 | a0001c0012t0018g0019a0003c0003t0003g0013a0003c0003t0003g0053others(12): Show | 19 | HG00639.hp1 HG01069.hp1 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.1264+275_1264+286d others(14): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778336 | |||||
chr2:17778336
|
GTATACAC others(23): Show |
G | 4 | a0002c0002t0002g0011a0002c0002t0002g0030a0002c0002t0002g0097others(1): Show | 7 | HG00735.hp1 HG01109.hp1 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.1264+287_1264+316d others(32): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778336 | |||||
chr2:17778339
|
T | C | 4 | a0003c0003t0003g0023a0003c0003t0003g0059a0003c0003t0003g0117others(1): Show | 5 | HG01243.hp1 HG02451.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1264+276T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778339 | ||||||
chr2:17778339
|
T | TATAC | 5 | a0007c0007t0002g0012a0007c0007t0002g0025a0007c0007t0017g0109others(2): Show | 8 | HG02559.hp2 HG02615.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1264+277_1264+278i others(6): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778339 | |||||
chr2:17778341
|
C | T | 13 | a0001c0001t0001g0128a0001c0001t0001g0155a0001c0001t0001g0166others(10): Show | 14 | HG01109.hp2 HG02074.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.1264+278C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778341 | ||||||
chr2:17778345
|
C | T | 5 | a0003c0003t0003g0007a0003c0003t0003g0046a0003c0003t0003g0060others(2): Show | 7 | HG01261.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1264+282C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778345 | ||||||
chr2:17778347
|
C | CAT | 26 | a0002c0002t0002g0009a0002c0002t0002g0010a0002c0002t0002g0020others(23): Show | 35 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(32): Show |
intron_variant | MODIFIER | c.1264+285_1264+286d others(4): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778347 | |||||
chr2:17778347
|
C | CATGTGTA others(23): Show |
1 | a0002c0002t0046g0083 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1264+290_1264+291i others(32): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778347 | |||||
chr2:17778347
|
C | CATGTGTG others(21): Show |
1 | a0010c0010t0002g0093 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1264+305_1264+306i others(30): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778347 | |||||
chr2:17778347
|
C | T | 19 | a0001c0001t0001g0133a0001c0001t0037g0189a0003c0003t0003g0007others(16): Show | 25 | HG01243.hp1 HG01261.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.1264+284C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778347 | ||||||
chr2:17778348
|
A | ATG | 15 | a0001c0001t0001g0014a0001c0001t0001g0035a0001c0001t0001g0038others(12): Show | 20 | HG00408.hp2 HG00741.hp2 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.1264+291_1264+292d others(4): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778348 | |||||
chr2:17778348
|
A | G | 9 | a0001c0001t0001g0043a0001c0001t0001g0131a0001c0001t0001g0133others(6): Show | 10 | HG01069.hp2 HG02717.hp1 HG03225.hp2 others(7): Show |
intron_variant | MODIFIER | c.1264+285A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778348 | ||||||
chr2:17778349
|
T | C | 6 | a0002c0002t0007g0027a0008c0008t0012g0104a0008c0008t0012g0105others(3): Show | 8 | HG01109.hp2 HG02258.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.1264+286T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778349 | ||||||
chr2:17778350
|
G | A | 1 | a0008c0008t0016g0033 | 2 | HG02258.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1264+287G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778350 | ||||||
chr2:17778350
|
G | ATGTGTAC others(25): Show |
1 | a0002c0002t0007g0027 | 2 | HG03041.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1264+286_1264+287i others(34): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778350 | ||||||
chr2:17778364
|
GTA | G | 7 | a0002c0002t0002g0092a0003c0003t0003g0007a0003c0003t0003g0046others(4): Show | 9 | HG01891.hp2 HG02145.hp1 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.1264+306_1264+307d others(4): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778364 | |||||
chr2:17778364
|
GTATA | G | 4 | a0003c0003t0003g0013a0003c0003t0020g0013a0003c0003t0048g0056others(1): Show | 5 | HG00639.hp1 HG01074.hp2 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.1264+304_1264+307d others(6): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778364 | |||||
chr2:17778367
|
T | C | 1 | a0003c0019t0003g0068 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1264+304T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778367 | ||||||
chr2:17778367
|
TATAC | T | 10 | a0003c0003t0003g0055a0003c0003t0003g0061a0003c0003t0003g0062others(7): Show | 12 | HG01069.hp1 HG01070.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.1264+306_1264+309d others(6): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778367 | |||||
chr2:17778368
|
A | G | 2 | a0003c0003t0003g0023a0003c0003t0003g0059 | 3 | HG01243.hp1 HG02451.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1264+305A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778368 | ||||||
chr2:17778369
|
T | C | 3 | a0003c0019t0003g0068a0011c0011t0015g0072a0011c0011t0015g0074 | 3 | HG00140.hp1 HG03669.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1264+306T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778369 | ||||||
chr2:17778369
|
TAC | T | 4 | a0002c0002t0002g0082a0002c0002t0002g0087a0002c0002t0007g0008others(1): Show | 6 | HG01099.hp2 HG02055.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1264+314_1264+315d others(4): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778369 | |||||
chr2:17778371
|
C | CACGCACA others(21): Show |
1 | a0008c0008t0016g0033 | 2 | HG02258.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1264+310_1264+311i others(30): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778371 | |||||
chr2:17778371
|
CACACACA others(25): Show |
C | 1 | a0002c0002t0045g0084 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1264+348_1264+379d others(34): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778371 | |||||
chr2:17778373
|
C | CACATATG others(19): Show |
1 | a0007c0007t0032g0107 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1264+313_1264+314i others(28): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778373 | |||||
chr2:17778375
|
CACAT | C | 18 | a0001c0001t0001g0125a0001c0001t0001g0128a0001c0001t0001g0154others(15): Show | 21 | HG01975.hp1 HG02074.hp1 HG02559.hp2 others(18): Show |
intron_variant | MODIFIER | c.1264+314_1264+317d others(6): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778375 | |||||
chr2:17778375
|
CACATAT | C | 98 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(95): Show | 148 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.1264+314_1264+319d others(8): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778375 | |||||
chr2:17778377
|
C | T | 2 | a0002c0002t0002g0100a0003c0019t0003g0068 | 2 | HG00140.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.1264+314C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778377 | ||||||
chr2:17778379
|
T | C | 19 | a0002c0002t0002g0085a0003c0003t0003g0061a0005c0005t0005g0002others(16): Show | 35 | HG00621.hp2 HG00639.hp2 HG01261.hp1 others(32): Show |
intron_variant | MODIFIER | c.1264+316T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778379 | ||||||
chr2:17778379
|
T | TATGTGTG others(25): Show |
1 | a0008c0008t0012g0104 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1264+318_1264+319i others(34): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778379 | |||||
chr2:17778379
|
T | TATGTGTG others(57): Show |
3 | a0008c0008t0012g0105a0008c0008t0012g0106a0012c0013t0012g0103 | 3 | HG02886.hp2 HG02965.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1264+318_1264+319i others(66): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778379 | |||||
chr2:17778380
|
A | G | 1 | a0003c0019t0003g0068 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1264+317A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778380 | ||||||
chr2:17778381
|
T | TATGTATA others(7): Show |
1 | a0001c0001t0001g0156 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1264+322_1264+323i others(16): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778381 | |||||
chr2:17778382
|
A | G | 42 | a0001c0001t0001g0122a0001c0001t0001g0186a0002c0002t0002g0009others(39): Show | 50 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.1264+319A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778382 | ||||||
chr2:17778390
|
A | G | 3 | a0001c0001t0001g0123a0001c0001t0001g0169a0001c0001t0001g0210 | 3 | HG01106.hp2 HG01358.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.1264+327A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778390 | ||||||
chr2:17778394
|
A | G | 8 | a0005c0005t0005g0002a0005c0005t0005g0112a0005c0005t0008g0002others(5): Show | 20 | HG00621.hp2 HG00639.hp2 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.1264+331A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778394 | ||||||
chr2:17778398
|
GTA | G | 7 | a0001c0001t0001g0170a0003c0003t0003g0007a0003c0003t0003g0046others(4): Show | 9 | HG01261.hp1 HG01891.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1264+340_1264+341d others(4): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778398 | |||||
chr2:17778400
|
A | ATG | 5 | a0003c0003t0003g0023a0003c0003t0003g0057a0003c0003t0003g0059others(2): Show | 6 | HG01243.hp1 HG01884.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1264+338_1264+339i others(4): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778400 | |||||
chr2:17778403
|
T | C | 12 | a0003c0003t0003g0007a0003c0003t0003g0023a0003c0003t0003g0046others(9): Show | 15 | HG01243.hp1 HG01261.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.1264+340T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778403 | ||||||
chr2:17778403
|
T | TAC | 57 | a0001c0012t0018g0019a0002c0002t0002g0010a0002c0002t0002g0011others(54): Show | 73 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.1264+346_1264+347d others(4): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778403 | |||||
chr2:17778403
|
T | TACACACA others(25): Show |
1 | a0002c0002t0002g0086 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1264+350_1264+351i others(34): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778403 | |||||
chr2:17778409
|
CAT | C | 111 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(108): Show | 176 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.1264+351_1264+352d others(4): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778409 | |||||
chr2:17778409
|
CATATATG others(5): Show |
C | 15 | a0001c0001t0001g0125a0001c0001t0001g0128a0001c0001t0001g0154others(12): Show | 15 | HG01975.hp1 HG02074.hp1 HG03831.hp2 others(12): Show |
intron_variant | MODIFIER | c.1264+348_1264+359d others(14): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778409 | |||||
chr2:17778411
|
T | C | 15 | a0001c0001t0001g0170a0003c0003t0003g0055a0003c0003t0003g0062others(12): Show | 18 | HG01069.hp1 HG01070.hp2 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.1264+348T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778411 | ||||||
chr2:17778412
|
A | G | 2 | a0003c0003t0003g0053a0003c0003t0003g0117 | 2 | HG01934.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1264+349A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778412 | ||||||
chr2:17778413
|
T | C | 2 | a0003c0003t0003g0062a0009c0009t0019g0052 | 2 | HG03710.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1264+350T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778413 | ||||||
chr2:17778414
|
A | G | 28 | a0001c0001t0001g0165a0001c0001t0001g0181a0003c0003t0003g0007others(25): Show | 34 | HG00140.hp1 HG00639.hp1 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.1264+351A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778414 | ||||||
chr2:17778416
|
GTGTGTAC others(9): Show |
G | 1 | a0003c0003t0003g0047 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1264+355_1264+370d others(18): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778416 | |||||
chr2:17778419
|
TGTACATA others(31): Show |
T | 2 | a0003c0003t0003g0053a0003c0003t0003g0117 | 2 | HG01934.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1264+357_1264+394d others(40): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778419 | ||||||
chr2:17778435
|
TAC | T | 37 | a0003c0003t0003g0007a0003c0003t0003g0013a0003c0003t0003g0023others(34): Show | 44 | HG00140.hp1 HG00639.hp1 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.1264+380_1264+381d others(4): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778435 | |||||
chr2:17778437
|
C | T | 1 | a0003c0003t0003g0047 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1264+374C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778437 | ||||||
chr2:17778439
|
C | CACATATA others(7): Show |
2 | a0001c0001t0001g0005a0001c0001t0001g0130 | 6 | NA18942.hp2 NA18977.hp1 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.1264+379_1264+380i others(16): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778439 | |||||
chr2:17778439
|
C | CACATATG others(9): Show |
2 | a0001c0001t0001g0043a0001c0001t0001g0200 | 3 | HG02717.hp1 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1264+379_1264+380i others(18): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778439 | |||||
chr2:17778443
|
C | T | 30 | a0001c0001t0001g0125a0001c0001t0001g0128a0001c0001t0001g0154others(27): Show | 46 | HG00621.hp2 HG00639.hp2 HG01975.hp1 others(43): Show |
intron_variant | MODIFIER | c.1264+380C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778443 | ||||||
chr2:17778445
|
T | C | 5 | a0001c0001t0001g0005a0001c0001t0001g0043a0001c0001t0001g0130others(2): Show | 10 | HG02717.hp1 HG02965.hp1 HG03225.hp2 others(7): Show |
intron_variant | MODIFIER | c.1264+382T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778445 | ||||||
chr2:17778445
|
T | TATGTATA others(7): Show |
1 | a0001c0001t0001g0174 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1264+384_1264+385i others(16): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778445 | |||||
chr2:17778446
|
A | G | 69 | a0001c0001t0001g0125a0001c0001t0001g0128a0001c0001t0001g0154others(66): Show | 92 | HG00140.hp1 HG00621.hp2 HG00639.hp1 others(89): Show |
intron_variant | MODIFIER | c.1264+383A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778446 | ||||||
chr2:17778450
|
G | GTATATAC others(11): Show |
1 | a0001c0001t0001g0127 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1264+388_1264+389i others(20): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778450 | |||||
chr2:17778452
|
G | A | 98 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(95): Show | 148 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.1264+389G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778452 | ||||||
chr2:17778453
|
TGTAC | T | 69 | a0001c0001t0001g0125a0001c0001t0001g0128a0001c0001t0001g0154others(66): Show | 92 | HG00140.hp1 HG00621.hp2 HG00639.hp1 others(89): Show |
intron_variant | MODIFIER | c.1264+391_1264+394d others(6): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778453 | ||||||
chr2:17778454
|
G | A | 93 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0014others(90): Show | 138 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.1264+391G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778454 | ||||||
chr2:17778456
|
A | G | 5 | a0001c0001t0001g0005a0001c0001t0001g0043a0001c0001t0001g0130others(2): Show | 10 | HG02717.hp1 HG03225.hp2 HG03453.hp2 others(7): Show |
intron_variant | MODIFIER | c.1264+393A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778456 | ||||||
chr2:17778457
|
C | CACACATA others(9): Show |
93 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0014others(90): Show | 138 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.1264+395_1264+396i others(18): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778457 | |||||
chr2:17778457
|
C | T | 6 | a0001c0001t0001g0005a0001c0001t0001g0043a0001c0001t0001g0127others(3): Show | 11 | HG02717.hp1 HG03225.hp2 HG03453.hp2 others(8): Show |
intron_variant | MODIFIER | c.1264+394C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778457 | ||||||
chr2:17778458
|
A | C | 1 | a0001c0001t0001g0127 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1264+395A>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778458 | ||||||
chr2:17778460
|
A | C | 169 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(166): Show | 242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.1264+397A>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778460 | ||||||
chr2:17778461
|
T | C | 1 | a0001c0001t0001g0127 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1264+398T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778461 | ||||||
chr2:17778464
|
G | A | 170 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(167): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.1264+401G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778464 | ||||||
chr2:17778469
|
T | C | 1 | a0001c0012t0018g0019 | 2 | HG02572.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1264+406T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778469 | ||||||
chr2:17778588
|
CTT | C | 41 | a0003c0003t0003g0007a0003c0003t0003g0013a0003c0003t0003g0023others(38): Show | 48 | HG00140.hp1 HG00639.hp1 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.1264+527_1264+528d others(4): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778588 | |||||
chr2:17778678
|
A | G | 7 | a0001c0001t0009g0015a0001c0001t0009g0139a0001c0001t0009g0140others(4): Show | 8 | HG00099.hp2 HG00280.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.1264+615A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17778678 | ||||||
chr2:17778777
|
CT | C | 56 | a0001c0012t0018g0019a0003c0003t0003g0007a0003c0003t0003g0013others(53): Show | 79 | HG00140.hp1 HG00621.hp2 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.1264+725delT | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778777 | |||||
chr2:17778828
|
A | ATTATTC | 8 | a0005c0005t0005g0002a0005c0005t0005g0112a0005c0005t0008g0002others(5): Show | 20 | HG00621.hp2 HG00639.hp2 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.1264+771_1264+776d others(8): Show |
GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 17778828 | |||||
chr2:17779013
|
T | C | 1 | a0004c0004t0001g0203 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1264+950T>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17779013 | ||||||
chr2:17779143
|
G | T | 115 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(112): Show | 165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.1265-835G>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17779143 | ||||||
chr2:17779189
|
C | T | 1 | a0004c0004t0001g0204 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1265-789C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17779189 | ||||||
chr2:17779194
|
A | G | 85 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(82): Show | 120 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.1265-784A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17779194 | ||||||
chr2:17779453
|
C | T | 1 | a0001c0001t0001g0127 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1265-525C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17779453 | ||||||
chr2:17779553
|
C | G | 1 | a0015c0015t0040g0121 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1265-425C>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17779553 | ||||||
chr2:17779622
|
A | G | 1 | a0004c0004t0001g0041 | 2 | NA18964.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.1265-356A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17779622 | ||||||
chr2:17779670
|
C | T | 1 | a0001c0001t0001g0160 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1265-308C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17779670 | ||||||
chr2:17779682
|
A | G | 1 | a0001c0001t0001g0173 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1265-296A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17779682 | ||||||
chr2:17779694
|
C | T | 1 | a0001c0001t0001g0162 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1265-284C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17779694 | ||||||
chr2:17779709
|
C | G | 2 | a0007c0007t0017g0109a0007c0007t0017g0110 | 2 | HG03130.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1265-269C>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17779709 | ||||||
chr2:17779714
|
G | T | 1 | a0001c0001t0001g0160 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1265-264G>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17779714 | ||||||
chr2:17779783
|
A | G | 184 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(181): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.1265-195A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17779783 | ||||||
chr2:17779862
|
C | T | 12 | a0003c0003t0006g0024a0003c0003t0006g0064a0003c0003t0006g0065others(9): Show | 13 | HG01884.hp1 HG02056.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1265-116C>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17779862 | ||||||
chr2:17779863
|
G | A | 2 | a0003c0003t0003g0060a0003c0003t0003g0061 | 2 | HG01261.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1265-115G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17779863 | ||||||
chr2:17779920
|
G | T | 2 | a0003c0003t0003g0055a0003c0003t0049g0049 | 2 | HG01496.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1265-58G>T | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 12/13 | chr2 | 17779920 | ||||||
chr2:17780137
|
G | A | 1 | a0010c0010t0002g0094 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1408+16G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 13/13 | chr2 | 17780137 | ||||||
chr2:17780153
|
A | C | 2 | a0001c0001t0001g0172a0001c0001t0001g0199 | 2 | NA18972.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.1408+32A>C | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 13/13 | chr2 | 17780153 | ||||||
chr2:17780334
|
C | G | 8 | a0005c0005t0005g0002a0005c0005t0005g0112a0005c0005t0008g0002others(5): Show | 20 | HG00621.hp2 HG00639.hp2 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.1408+213C>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 13/13 | chr2 | 17780334 | ||||||
chr2:17780395
|
G | A | 2 | a0002c0002t0002g0092a0008c0008t0041g0045 | 2 | HG02886.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1409-226G>A | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 13/13 | chr2 | 17780395 | ||||||
chr2:17780524
|
A | G | 1 | a0001c0001t0001g0171 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1409-97A>G | GEN1 | ENSG00000178295.15 | transcript | ENST00000381254.7 | protein_coding | 13/13 | chr2 | 17780524 |