geneid | 123722 |
---|---|
ensemblid | ENSG00000186628.12 |
hgncid | 18024 |
symbol | FSD2 |
name | fibronectin type III and SPRY domain containing 2 |
refseq_nuc | NM_001007122.4 |
refseq_prot | NP_001007123.1 |
ensembl_nuc | ENST00000334574.12 |
ensembl_prot | ENSP00000335651.8 |
mane_status | MANE Select |
chr | chr15 |
start | 82755362 |
end | 82806069 |
strand | - |
ver | v1.2 |
region | chr15:82755362-82806069 |
region5000 | chr15:82750362-82811069 |
regionname0 | FSD2_chr15_82755362_82806069 |
regionname5000 | FSD2_chr15_82750362_82811069 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 749 | 300 | 77 | 53 | 132 | 13 | 24 | 100 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0002 | 0/0 | 749 | 53 | 0 | 11 | 33 | 1 | 8 | 24 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0003 | 0/1 | 749 | 22 | 7 | 9 | 0 | 3 | 2 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0004 | 0/0 | 749 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0005 | 0/0 | 749 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0006 | 0/0 | 749 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0007 | 0/0 | 749 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0008 | 0/0 | 749 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0009 | 0/0 | 749 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0010 | 0/0 | 305 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 2250 | 199 | 56 | 32 | 84 | 8 | 18 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
c0002 | 0/0 | 2250 | 92 | 18 | 18 | 47 | 5 | 4 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
c0003 | 0/0 | 2250 | 53 | 0 | 11 | 33 | 1 | 8 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
c0004 | 0/1 | 2250 | 22 | 7 | 9 | 0 | 3 | 2 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
c0005 | 0/0 | 2250 | 5 | 0 | 3 | 0 | 0 | 2 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
c0006 | 0/0 | 2250 | 2 | 2 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
c0007 | 0/0 | 2250 | 2 | 2 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
c0008 | 0/0 | 2250 | 2 | 2 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
c0009 | 0/0 | 2250 | 1 | 0 | 0 | 0 | 1 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
c0010 | 0/0 | 2270 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
c0011 | 0/0 | 2250 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
c0012 | 0/0 | 2250 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
c0013 | 0/0 | 2250 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
c0014 | 0/0 | 2250 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
c0015 | 0/0 | 2250 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 4167 | 69 | 19 | 15 | 29 | 4 | 2 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
t0002 | 1/0 | 4169 | 59 | 9 | 9 | 22 | 3 | 15 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
t0003 | 0/0 | 4168 | 56 | 4 | 8 | 41 | 2 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
t0004 | 0/0 | 4168 | 42 | 0 | 10 | 25 | 0 | 7 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
t0005 | 0/1 | 4169 | 11 | 3 | 5 | 0 | 0 | 2 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
t0006 | 0/0 | 4170 | 11 | 4 | 4 | 0 | 2 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
t0007 | 0/0 | 4167 | 10 | 0 | 0 | 10 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
t0008 | 0/0 | 4167 | 9 | 9 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
t0009 | 0/0 | 4171 | 8 | 1 | 5 | 0 | 2 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
t0010 | 0/0 | 4168 | 7 | 0 | 0 | 7 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
t0011 | 0/0 | 4168 | 7 | 0 | 4 | 1 | 0 | 2 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
t0012 | 0/0 | 4168 | 6 | 0 | 1 | 4 | 1 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
t0013 | 0/0 | 4170 | 6 | 6 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
t0014 | 0/0 | 4169 | 4 | 4 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
t0015 | 0/0 | 4171 | 4 | 4 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
t0016 | 0/0 | 4166 | 4 | 0 | 0 | 2 | 1 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
t0017 | 0/0 | 4168 | 3 | 3 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
t0018 | 0/0 | 4169 | 3 | 0 | 1 | 1 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
t0019 | 0/0 | 4168 | 3 | 0 | 0 | 3 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
t0020 | 0/0 | 4169 | 3 | 0 | 1 | 0 | 2 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
t0021 | 0/0 | 4168 | 3 | 1 | 0 | 2 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
t0022 | 0/0 | 4168 | 3 | 0 | 2 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
t0023 | 0/0 | 4170 | 3 | 3 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
t0024 | 0/0 | 4170 | 3 | 0 | 3 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
t0025 | 0/0 | 4168 | 2 | 0 | 0 | 2 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
t0026 | 0/0 | 4167 | 2 | 1 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
t0027 | 0/0 | 4169 | 2 | 0 | 0 | 2 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
t0028 | 0/0 | 4168 | 2 | 0 | 0 | 2 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
t0029 | 0/0 | 4167 | 2 | 0 | 1 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
t0030 | 0/0 | 4170 | 2 | 2 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
t0031 | 0/0 | 4171 | 2 | 2 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
t0032 | 0/0 | 4170 | 2 | 2 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
t0033 | 0/0 | 4170 | 2 | 2 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
t0034 | 0/0 | 4166 | 2 | 0 | 0 | 2 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
t0035 | 0/0 | 4168 | 2 | 0 | 0 | 2 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
t0036 | 0/0 | 4168 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
t0037 | 0/0 | 4169 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
t0038 | 0/0 | 4168 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
t0039 | 0/0 | 4167 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
t0040 | 0/0 | 4168 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
t0041 | 0/0 | 4167 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
t0042 | 0/0 | 4169 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
t0043 | 0/0 | 4169 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
t0044 | 0/0 | 4170 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
t0045 | 0/0 | 4170 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
t0046 | 0/0 | 4169 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
t0047 | 0/0 | 4168 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
t0048 | 0/0 | 4170 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
t0049 | 0/0 | 4167 | 1 | 0 | 0 | 0 | 1 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
t0050 | 0/0 | 4169 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
t0051 | 0/0 | 4169 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
t0052 | 0/0 | 4167 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
t0053 | 0/0 | 4168 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
t0054 | 0/0 | 4169 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
t0055 | 0/0 | 4171 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
t0056 | 0/0 | 4167 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
t0057 | 0/0 | 4168 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
t0058 | 0/0 | 4167 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
t0059 | 0/0 | 4170 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
t0060 | 0/0 | 4167 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0005 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0008 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0135 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0308 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0356 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0366 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0368 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0374 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0375 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
g0376 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 2250 | 199 | 56 | 32 | 84 | 8 | 18 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0001c0002 | 0/0 | 2250 | 92 | 18 | 18 | 47 | 5 | 4 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0001c0005 | 0/0 | 2250 | 5 | 0 | 3 | 0 | 0 | 2 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0001c0008 | 0/0 | 2250 | 2 | 2 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0001c0011 | 0/0 | 2250 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0001c0012 | 0/0 | 2250 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0002c0003 | 0/0 | 2250 | 53 | 0 | 11 | 33 | 1 | 8 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0003c0004 | 0/1 | 2250 | 22 | 7 | 9 | 0 | 3 | 2 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0004c0006 | 0/0 | 2250 | 2 | 2 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0005c0007 | 0/0 | 2250 | 2 | 2 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0006c0009 | 0/0 | 2250 | 1 | 0 | 0 | 0 | 1 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0007c0015 | 0/0 | 2250 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0008c0013 | 0/0 | 2250 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0009c0014 | 0/0 | 2250 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0010c0010 | 0/0 | 2270 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002 | 1/0 | 6418 | 59 | 9 | 9 | 22 | 3 | 15 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0001c0001t0003 | 0/0 | 6417 | 55 | 4 | 8 | 41 | 1 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0001c0001t0006 | 0/0 | 6419 | 11 | 4 | 4 | 0 | 2 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0001c0001t0008 | 0/0 | 6416 | 8 | 8 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0001c0001t0009 | 0/0 | 6420 | 8 | 1 | 5 | 0 | 2 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0001c0001t0010 | 0/0 | 6417 | 7 | 0 | 0 | 7 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0001c0001t0011 | 0/0 | 6417 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0001c0001t0012 | 0/0 | 6417 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0001c0001t0013 | 0/0 | 6419 | 6 | 6 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0001c0001t0014 | 0/0 | 6418 | 4 | 4 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0001c0001t0015 | 0/0 | 6420 | 4 | 4 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0001c0001t0017 | 0/0 | 6417 | 3 | 3 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0001c0001t0021 | 0/0 | 6417 | 3 | 1 | 0 | 2 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0001c0001t0023 | 0/0 | 6419 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0001c0001t0024 | 0/0 | 6419 | 3 | 0 | 3 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0001c0001t0025 | 0/0 | 6417 | 2 | 0 | 0 | 2 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0001c0001t0026 | 0/0 | 6416 | 2 | 1 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0001c0001t0027 | 0/0 | 6418 | 2 | 0 | 0 | 2 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0001c0001t0028 | 0/0 | 6417 | 2 | 0 | 0 | 2 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0001c0001t0029 | 0/0 | 6416 | 2 | 0 | 1 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0001c0001t0030 | 0/0 | 6419 | 2 | 2 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0001c0001t0031 | 0/0 | 6420 | 2 | 2 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0001c0001t0035 | 0/0 | 6417 | 2 | 0 | 0 | 2 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0001c0001t0036 | 0/0 | 6417 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0001c0001t0037 | 0/0 | 6418 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0001c0001t0042 | 0/0 | 6418 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0001c0001t0043 | 0/0 | 6418 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0001c0001t0044 | 0/0 | 6419 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0001c0001t0048 | 0/0 | 6419 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0001c0001t0051 | 0/0 | 6418 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0001c0001t0055 | 0/0 | 6420 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0001c0001t0059 | 0/0 | 6419 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0001c0002t0001 | 0/0 | 6416 | 66 | 17 | 15 | 28 | 4 | 2 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0001c0002t0007 | 0/0 | 6416 | 10 | 0 | 0 | 10 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0001c0002t0016 | 0/0 | 6415 | 4 | 0 | 0 | 2 | 1 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0001c0002t0022 | 0/0 | 6417 | 3 | 0 | 2 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0001c0002t0034 | 0/0 | 6415 | 2 | 0 | 0 | 2 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0001c0002t0052 | 0/0 | 6416 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0001c0002t0053 | 0/0 | 6417 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0001c0002t0054 | 0/0 | 6418 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0001c0002t0056 | 0/0 | 6416 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0001c0002t0057 | 0/0 | 6417 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0001c0002t0058 | 0/0 | 6416 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0001c0002t0060 | 0/0 | 6416 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0001c0005t0011 | 0/0 | 6417 | 5 | 0 | 3 | 0 | 0 | 2 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0001c0008t0023 | 0/0 | 6419 | 2 | 2 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0001c0011t0008 | 0/0 | 6416 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0001c0012t0001 | 0/0 | 6416 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0002c0003t0004 | 0/0 | 6417 | 38 | 0 | 9 | 22 | 0 | 7 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0002c0003t0012 | 0/0 | 6417 | 5 | 0 | 1 | 3 | 1 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0002c0003t0018 | 0/0 | 6418 | 3 | 0 | 1 | 1 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0002c0003t0019 | 0/0 | 6417 | 3 | 0 | 0 | 3 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0002c0003t0038 | 0/0 | 6417 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0002c0003t0039 | 0/0 | 6416 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0002c0003t0040 | 0/0 | 6417 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0002c0003t0041 | 0/0 | 6416 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0003c0004t0005 | 0/1 | 6418 | 11 | 3 | 5 | 0 | 0 | 2 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0003c0004t0011 | 0/0 | 6417 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0003c0004t0020 | 0/0 | 6418 | 3 | 0 | 1 | 0 | 2 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0003c0004t0032 | 0/0 | 6419 | 2 | 2 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0003c0004t0045 | 0/0 | 6419 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0003c0004t0046 | 0/0 | 6418 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0003c0004t0047 | 0/0 | 6417 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0003c0004t0049 | 0/0 | 6416 | 1 | 0 | 0 | 0 | 1 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0003c0004t0050 | 0/0 | 6418 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0004c0006t0001 | 0/0 | 6416 | 2 | 2 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0005c0007t0033 | 0/0 | 6419 | 2 | 2 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0006c0009t0003 | 0/0 | 6417 | 1 | 0 | 0 | 0 | 1 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0007c0015t0004 | 0/0 | 6417 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0008c0013t0004 | 0/0 | 6417 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0009c0014t0004 | 0/0 | 6417 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
a0010c0010t0004 | 0/0 | 6437 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | copy fasta | chr15 | 82750362 | 82811069 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002g0005 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0008 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0006g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0006g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0006g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0006g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0006g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0006g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0006g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0006g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0006g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0006g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0006g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0008g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0008g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0008g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0008g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0008g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0008g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0008g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0008g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0009g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0009g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0009g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0009g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0009g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0009g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0009g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0009g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0010g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0010g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0010g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0010g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0010g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0010g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0010g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0011g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0012g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0013g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0013g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0013g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0013g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0013g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0013g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0014g0001 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0015g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0015g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0015g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0015g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0017g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0017g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0017g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0021g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0021g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0021g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0023g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0024g0374 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0024g0375 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0024g0376 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0025g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0025g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0026g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0026g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0027g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0027g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0028g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0028g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0029g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0029g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0030g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0030g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0031g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0031g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0035g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0035g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0036g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0037g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0042g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0043g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0044g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0048g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0051g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0055g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0059g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0007g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0007g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0007g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0007g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0007g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0007g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0007g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0007g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0007g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0007g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0016g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0016g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0016g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0016g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0022g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0022g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0022g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0034g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0034g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0052g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0053g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0054g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0056g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0057g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0058g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0060g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0005t0011g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0005t0011g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0005t0011g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0005t0011g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0008t0023g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0008t0023g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0011t0008g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0012t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0004g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0004g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0004g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0004g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0004g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0004g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0004g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0004g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0004g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0004g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0004g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0004g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0004g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0004g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0004g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0004g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0004g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0004g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0004g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0004g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0004g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0004g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0004g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0004g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0004g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0004g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0004g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0004g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0004g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0004g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0004g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0004g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0004g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0004g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0004g0366 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0004g0368 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0004g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0012g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0012g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0012g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0012g0356 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0012g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0018g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0018g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0018g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0019g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0019g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0019g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0038g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0039g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0040g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0041g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0003c0004t0005g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0003c0004t0005g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0003c0004t0005g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0003c0004t0005g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0003c0004t0005g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0003c0004t0005g0135 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0003c0004t0005g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0003c0004t0005g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0003c0004t0005g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0003c0004t0005g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0003c0004t0011g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0003c0004t0020g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0003c0004t0020g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0003c0004t0020g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0003c0004t0032g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0003c0004t0032g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0003c0004t0045g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0003c0004t0046g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0003c0004t0047g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0003c0004t0049g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0003c0004t0050g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0004c0006t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0004c0006t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0005c0007t0033g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0005c0007t0033g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0006c0009t0003g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0007c0015t0004g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0008c0013t0004g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0009c0014t0004g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0010c0010t0004g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0150 | EUR | GBR | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG00099 | hp2 | a0001 | c0001 | t0006 | g0019 | EUR | GBR | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG00140 | hp1 | a0001 | c0002 | t0001 | g0065 | EUR | GBR | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG00140 | hp2 | a0001 | c0001 | t0003 | g0014 | EUR | GBR | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG00280 | hp1 | a0002 | c0003 | t0012 | g0356 | EUR | FIN | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0005 | EUR | FIN | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG00323 | hp1 | a0001 | c0002 | t0001 | g0156 | EUR | FIN | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG00323 | hp2 | a0003 | c0004 | t0049 | g0131 | EUR | FIN | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | CHS | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG00408 | hp2 | a0001 | c0002 | t0001 | g0114 | EAS | CHS | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG00423 | hp1 | a0001 | c0002 | t0007 | g0319 | EAS | CHS | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG00423 | hp2 | a0002 | c0003 | t0004 | g0340 | EAS | CHS | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG00438 | hp1 | a0008 | c0013 | t0004 | g0081 | EAS | CHS | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0312 | EAS | CHS | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG00544 | hp1 | a0002 | c0003 | t0004 | g0222 | EAS | CHS | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG00544 | hp2 | a0001 | c0001 | t0003 | g0184 | EAS | CHS | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG00558 | hp1 | a0001 | c0001 | t0003 | g0203 | EAS | CHS | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0305 | EAS | CHS | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0297 | EAS | CHS | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG00597 | hp2 | a0001 | c0001 | t0003 | g0177 | EAS | CHS | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG00609 | hp1 | a0001 | c0002 | t0001 | g0077 | EAS | CHS | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG00609 | hp2 | a0001 | c0001 | t0003 | g0210 | EAS | CHS | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG00639 | hp1 | a0001 | c0002 | t0001 | g0157 | AMR | PUR | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG00639 | hp2 | a0001 | c0005 | t0011 | g0372 | AMR | PUR | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG00673 | hp1 | a0001 | c0002 | t0007 | g0144 | EAS | CHS | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG00673 | hp2 | a0001 | c0001 | t0003 | g0259 | EAS | CHS | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0293 | AMR | PUR | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG00733 | hp2 | a0002 | c0003 | t0004 | g0370 | AMR | PUR | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG00735 | hp1 | a0001 | c0005 | t0011 | g0373 | AMR | PUR | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG00735 | hp2 | a0007 | c0015 | t0004 | g0146 | AMR | PUR | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0310 | AMR | PUR | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG00738 | hp2 | a0003 | c0004 | t0046 | g0129 | AMR | PUR | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG00741 | hp1 | a0003 | c0004 | t0045 | g0142 | AMR | PUR | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG00741 | hp2 | a0001 | c0001 | t0003 | g0321 | AMR | PUR | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01069 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01069 | hp2 | a0001 | c0001 | t0003 | g0140 | AMR | PUR | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01070 | hp1 | a0001 | c0001 | t0024 | g0375 | AMR | PUR | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01070 | hp2 | a0001 | c0001 | t0029 | g0207 | AMR | PUR | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01071 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01071 | hp2 | a0001 | c0001 | t0024 | g0374 | AMR | PUR | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01074 | hp1 | a0001 | c0001 | t0003 | g0262 | AMR | PUR | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01074 | hp2 | a0003 | c0004 | t0020 | g0223 | AMR | PUR | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01099 | hp1 | a0003 | c0004 | t0005 | g0180 | AMR | PUR | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01099 | hp2 | a0001 | c0001 | t0003 | g0026 | AMR | PUR | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01106 | hp1 | a0001 | c0001 | t0006 | g0024 | AMR | PUR | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01106 | hp2 | a0001 | c0001 | t0003 | g0141 | AMR | PUR | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01109 | hp1 | a0001 | c0002 | t0022 | g0225 | AMR | PUR | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01109 | hp2 | a0001 | c0001 | t0026 | g0246 | AMR | PUR | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0309 | AMR | PUR | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01167 | hp2 | a0003 | c0004 | t0005 | g0003 | AMR | PUR | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01169 | hp1 | a0003 | c0004 | t0005 | g0003 | AMR | PUR | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0153 | AMR | PUR | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0296 | AMR | PUR | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01175 | hp2 | a0002 | c0003 | t0004 | g0362 | AMR | PUR | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0151 | AMR | PUR | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01192 | hp2 | a0001 | c0001 | t0006 | g0016 | AMR | PUR | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01243 | hp1 | a0001 | c0002 | t0001 | g0062 | AMR | PUR | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01243 | hp2 | a0001 | c0002 | t0001 | g0113 | AMR | PUR | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01257 | hp1 | a0001 | c0001 | t0003 | g0211 | AMR | CLM | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01257 | hp2 | a0001 | c0001 | t0009 | g0050 | AMR | CLM | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01258 | hp1 | a0003 | c0004 | t0005 | g0133 | AMR | CLM | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01258 | hp2 | a0001 | c0001 | t0009 | g0011 | AMR | CLM | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01261 | hp1 | a0001 | c0001 | t0003 | g0202 | AMR | CLM | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01261 | hp2 | a0001 | c0001 | t0024 | g0376 | AMR | CLM | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01346 | hp1 | a0001 | c0002 | t0001 | g0067 | AMR | CLM | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01346 | hp2 | a0001 | c0001 | t0006 | g0119 | AMR | CLM | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0152 | AMR | CLM | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01358 | hp2 | a0003 | c0004 | t0005 | g0132 | AMR | CLM | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01361 | hp1 | a0001 | c0001 | t0009 | g0022 | AMR | CLM | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01361 | hp2 | a0001 | c0005 | t0011 | g0371 | AMR | CLM | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0292 | AMR | CLM | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01433 | hp2 | a0001 | c0001 | t0009 | g0028 | AMR | CLM | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01515 | hp1 | a0001 | c0001 | t0006 | g0017 | EUR | IBS | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01515 | hp2 | a0003 | c0004 | t0020 | g0134 | EUR | IBS | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01516 | hp1 | a0001 | c0001 | t0009 | g0020 | EUR | IBS | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01516 | hp2 | a0001 | c0002 | t0016 | g0066 | EUR | IBS | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01517 | hp1 | a0001 | c0002 | t0001 | g0059 | EUR | IBS | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01517 | hp2 | a0003 | c0004 | t0020 | g0137 | EUR | IBS | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01884 | hp1 | a0001 | c0001 | t0009 | g0018 | AFR | ACB | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01884 | hp2 | a0001 | c0008 | t0023 | g0286 | AFR | ACB | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01891 | hp1 | a0001 | c0001 | t0023 | g0009 | AFR | ACB | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0121 | AFR | ACB | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01928 | hp1 | a0002 | c0003 | t0004 | g0147 | AMR | PEL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01928 | hp2 | a0001 | c0002 | t0001 | g0074 | AMR | PEL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01934 | hp1 | a0002 | c0003 | t0004 | g0004 | AMR | PEL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01934 | hp2 | a0001 | c0001 | t0037 | g0260 | AMR | PEL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01943 | hp1 | a0001 | c0002 | t0001 | g0073 | AMR | PEL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01943 | hp2 | a0002 | c0003 | t0004 | g0004 | AMR | PEL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01952 | hp1 | a0001 | c0002 | t0022 | g0093 | AMR | PEL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0311 | AMR | PEL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01975 | hp1 | a0002 | c0003 | t0012 | g0355 | AMR | PEL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01975 | hp2 | a0001 | c0002 | t0060 | g0110 | AMR | PEL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01978 | hp1 | a0001 | c0001 | t0006 | g0025 | AMR | PEL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01978 | hp2 | a0002 | c0003 | t0018 | g0357 | AMR | PEL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01981 | hp1 | a0001 | c0001 | t0003 | g0261 | AMR | PEL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01981 | hp2 | a0001 | c0002 | t0001 | g0012 | AMR | PEL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01993 | hp1 | a0002 | c0003 | t0004 | g0352 | AMR | PEL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01993 | hp2 | a0001 | c0002 | t0001 | g0079 | AMR | PEL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02004 | hp1 | a0001 | c0001 | t0009 | g0023 | AMR | PEL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02004 | hp2 | a0001 | c0002 | t0001 | g0283 | AMR | PEL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02015 | hp1 | a0001 | c0001 | t0003 | g0188 | EAS | KHV | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02015 | hp2 | a0002 | c0003 | t0004 | g0339 | EAS | KHV | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02040 | hp1 | a0001 | c0001 | t0003 | g0204 | EAS | KHV | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02040 | hp2 | a0002 | c0003 | t0004 | g0342 | EAS | KHV | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02055 | hp1 | a0001 | c0001 | t0008 | g0239 | AFR | ACB | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02055 | hp2 | a0001 | c0002 | t0001 | g0106 | AFR | ACB | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02056 | hp1 | a0001 | c0001 | t0003 | g0192 | EAS | KHV | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02056 | hp2 | a0001 | c0001 | t0011 | g0007 | EAS | KHV | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02071 | hp1 | a0002 | c0003 | t0019 | g0333 | EAS | KHV | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02071 | hp2 | a0001 | c0001 | t0003 | g0201 | EAS | KHV | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02074 | hp1 | a0001 | c0001 | t0003 | g0088 | EAS | KHV | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02074 | hp2 | a0001 | c0002 | t0001 | g0098 | EAS | KHV | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0275 | EAS | KHV | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02080 | hp2 | a0001 | c0002 | t0001 | g0123 | EAS | KHV | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02083 | hp1 | a0002 | c0003 | t0004 | g0347 | EAS | KHV | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02083 | hp2 | a0001 | c0002 | t0001 | g0115 | EAS | KHV | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02132 | hp1 | a0001 | c0001 | t0003 | g0306 | EAS | KHV | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02132 | hp2 | a0002 | c0003 | t0038 | g0369 | EAS | KHV | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02135 | hp1 | a0001 | c0002 | t0001 | g0058 | EAS | KHV | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02135 | hp2 | a0001 | c0001 | t0003 | g0302 | EAS | KHV | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02148 | hp1 | a0002 | c0003 | t0004 | g0361 | AMR | PEL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02148 | hp2 | a0001 | c0002 | t0001 | g0080 | AMR | PEL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02155 | hp1 | a0001 | c0002 | t0001 | g0094 | EAS | CDX | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02155 | hp2 | a0001 | c0001 | t0003 | g0205 | EAS | CDX | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02165 | hp1 | a0002 | c0003 | t0004 | g0341 | EAS | CDX | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02165 | hp2 | a0001 | c0002 | t0007 | g0277 | EAS | CDX | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02257 | hp1 | a0001 | c0001 | t0015 | g0219 | AFR | ACB | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02257 | hp2 | a0001 | c0002 | t0001 | g0055 | AFR | ACB | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02273 | hp1 | a0003 | c0004 | t0011 | g0032 | AMR | PEL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02273 | hp2 | a0001 | c0002 | t0001 | g0078 | AMR | PEL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02280 | hp1 | a0001 | c0002 | t0001 | g0247 | AFR | ACB | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02280 | hp2 | a0001 | c0002 | t0001 | g0060 | AFR | ACB | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02293 | hp1 | a0001 | c0002 | t0001 | g0013 | AMR | PEL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02293 | hp2 | a0002 | c0003 | t0004 | g0332 | AMR | PEL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02300 | hp1 | a0001 | c0002 | t0001 | g0118 | AMR | PEL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02300 | hp2 | a0002 | c0003 | t0004 | g0328 | AMR | PEL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02451 | hp1 | a0001 | c0001 | t0003 | g0258 | AFR | ACB | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02451 | hp2 | a0001 | c0001 | t0008 | g0214 | AFR | ACB | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0320 | EAS | KHV | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02523 | hp2 | a0001 | c0002 | t0001 | g0092 | EAS | KHV | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02572 | hp1 | a0001 | c0001 | t0015 | g0278 | AFR | GWD | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02572 | hp2 | a0003 | c0004 | t0050 | g0136 | AFR | GWD | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02602 | hp1 | a0002 | c0003 | t0004 | g0353 | SAS | PJL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0300 | SAS | PJL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02615 | hp1 | a0001 | c0002 | t0001 | g0102 | AFR | GWD | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02615 | hp2 | a0003 | c0004 | t0005 | g0010 | AFR | GWD | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0267 | AFR | GWD | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02622 | hp2 | a0001 | c0001 | t0008 | g0270 | AFR | GWD | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02630 | hp1 | a0001 | c0002 | t0001 | g0104 | AFR | GWD | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02630 | hp2 | a0001 | c0001 | t0006 | g0285 | AFR | GWD | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0274 | AFR | GWD | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02647 | hp2 | a0001 | c0001 | t0008 | g0215 | AFR | GWD | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02683 | hp1 | a0001 | c0001 | t0006 | g0027 | SAS | PJL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0148 | SAS | PJL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02698 | hp1 | a0003 | c0004 | t0005 | g0179 | SAS | PJL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0314 | SAS | PJL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02717 | hp1 | a0001 | c0001 | t0042 | g0033 | AFR | GWD | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02717 | hp2 | a0001 | c0001 | t0008 | g0242 | AFR | GWD | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02735 | hp1 | a0001 | c0002 | t0016 | g0086 | SAS | PJL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0276 | SAS | PJL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02809 | hp1 | a0003 | c0004 | t0032 | g0125 | AFR | GWD | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02809 | hp2 | a0001 | c0001 | t0014 | g0001 | AFR | GWD | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02818 | hp1 | a0001 | c0001 | t0002 | g0268 | AFR | GWD | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02818 | hp2 | a0001 | c0001 | t0003 | g0169 | AFR | GWD | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02886 | hp1 | a0001 | c0001 | t0006 | g0120 | AFR | GWD | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02886 | hp2 | a0001 | c0002 | t0001 | g0240 | AFR | GWD | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02895 | hp1 | a0001 | c0001 | t0013 | g0167 | AFR | GWD | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02895 | hp2 | a0003 | c0004 | t0047 | g0130 | AFR | GWD | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02896 | hp1 | a0001 | c0001 | t0031 | g0217 | AFR | GWD | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02896 | hp2 | a0001 | c0001 | t0003 | g0233 | AFR | GWD | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02922 | hp1 | a0001 | c0002 | t0001 | g0327 | AFR | ESN | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02922 | hp2 | a0004 | c0006 | t0001 | g0100 | AFR | ESN | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02965 | hp1 | a0001 | c0008 | t0023 | g0287 | AFR | ESN | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02965 | hp2 | a0001 | c0001 | t0013 | g0178 | AFR | ESN | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02976 | hp1 | a0001 | c0001 | t0031 | g0218 | AFR | ESN | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02976 | hp2 | a0001 | c0001 | t0013 | g0324 | AFR | ESN | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0128 | SAS | PJL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG03017 | hp2 | a0001 | c0001 | t0003 | g0015 | SAS | PJL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG03041 | hp1 | a0001 | c0001 | t0015 | g0220 | AFR | GWD | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG03041 | hp2 | a0001 | c0002 | t0001 | g0101 | AFR | GWD | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG03098 | hp1 | a0001 | c0001 | t0017 | g0236 | AFR | MSL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG03098 | hp2 | a0001 | c0001 | t0048 | g0265 | AFR | MSL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0175 | AFR | ESN | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG03130 | hp2 | a0001 | c0002 | t0001 | g0161 | AFR | ESN | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG03139 | hp1 | a0001 | c0002 | t0001 | g0030 | AFR | ESN | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG03139 | hp2 | a0001 | c0001 | t0043 | g0166 | AFR | ESN | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG03195 | hp1 | a0003 | c0004 | t0005 | g0154 | AFR | ESN | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG03195 | hp2 | a0001 | c0001 | t0014 | g0001 | AFR | ESN | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG03209 | hp1 | a0001 | c0001 | t0013 | g0282 | AFR | MSL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG03209 | hp2 | a0001 | c0001 | t0017 | g0263 | AFR | MSL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG03225 | hp1 | a0001 | c0001 | t0015 | g0221 | AFR | MSL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG03225 | hp2 | a0001 | c0001 | t0002 | g0295 | AFR | MSL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG03453 | hp1 | a0001 | c0002 | t0056 | g0103 | AFR | MSL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0266 | AFR | MSL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG03486 | hp1 | a0001 | c0001 | t0008 | g0271 | AFR | MSL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG03486 | hp2 | a0001 | c0001 | t0030 | g0288 | AFR | MSL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG03490 | hp1 | a0001 | c0005 | t0011 | g0006 | SAS | PJL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0127 | SAS | PJL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG03492 | hp1 | a0001 | c0005 | t0011 | g0006 | SAS | PJL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0299 | SAS | PJL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG03540 | hp1 | a0001 | c0002 | t0001 | g0063 | AFR | GWD | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG03540 | hp2 | a0001 | c0001 | t0026 | g0248 | AFR | GWD | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG03579 | hp1 | a0001 | c0001 | t0030 | g0289 | AFR | MSL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG03579 | hp2 | a0001 | c0001 | t0059 | g0124 | AFR | MSL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0087 | SAS | PJL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG03654 | hp2 | a0002 | c0003 | t0004 | g0348 | SAS | PJL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG03704 | hp1 | a0001 | c0002 | t0001 | g0051 | SAS | PJL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG03704 | hp2 | a0002 | c0003 | t0018 | g0346 | SAS | PJL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG03710 | hp1 | a0003 | c0004 | t0005 | g0126 | SAS | PJL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0298 | SAS | PJL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0322 | SAS | BEB | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG03831 | hp2 | a0002 | c0003 | t0004 | g0281 | SAS | BEB | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0139 | SAS | BEB | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG03942 | hp2 | a0001 | c0002 | t0001 | g0075 | SAS | BEB | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG04115 | hp1 | a0002 | c0003 | t0004 | g0368 | SAS | STU | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0149 | SAS | STU | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG04184 | hp1 | a0001 | c0002 | t0054 | g0069 | SAS | BEB | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG04184 | hp2 | a0002 | c0003 | t0004 | g0360 | SAS | BEB | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG04199 | hp1 | a0002 | c0003 | t0004 | g0334 | SAS | STU | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG04199 | hp2 | a0001 | c0001 | t0051 | g0315 | SAS | STU | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0084 | SAS | STU | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0301 | SAS | STU | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18522 | hp1 | a0001 | c0001 | t0014 | g0001 | AFR | YRI | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18522 | hp2 | a0001 | c0002 | t0001 | g0241 | AFR | YRI | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18612 | hp1 | a0002 | c0003 | t0004 | g0326 | EAS | CHB | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18612 | hp2 | a0001 | c0001 | t0003 | g0181 | EAS | CHB | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18906 | hp1 | a0001 | c0001 | t0006 | g0213 | AFR | YRI | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18906 | hp2 | a0001 | c0001 | t0017 | g0235 | AFR | YRI | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18941 | hp1 | a0001 | c0001 | t0003 | g0206 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18941 | hp2 | a0001 | c0002 | t0001 | g0159 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18942 | hp1 | a0002 | c0003 | t0004 | g0335 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18942 | hp2 | a0001 | c0001 | t0003 | g0273 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18944 | hp1 | a0001 | c0001 | t0003 | g0252 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18944 | hp2 | a0002 | c0003 | t0004 | g0111 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18945 | hp1 | a0001 | c0012 | t0001 | g0064 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18945 | hp2 | a0002 | c0003 | t0004 | g0364 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18947 | hp1 | a0001 | c0002 | t0057 | g0053 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18947 | hp2 | a0001 | c0001 | t0003 | g0173 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18950 | hp1 | a0001 | c0002 | t0001 | g0090 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18950 | hp2 | a0001 | c0001 | t0003 | g0170 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0294 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18951 | hp2 | a0001 | c0001 | t0003 | g0193 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18953 | hp1 | a0001 | c0001 | t0003 | g0250 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18953 | hp2 | a0002 | c0003 | t0039 | g0325 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18956 | hp1 | a0001 | c0002 | t0001 | g0037 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18956 | hp2 | a0001 | c0002 | t0034 | g0072 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18957 | hp1 | a0001 | c0001 | t0003 | g0183 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18957 | hp2 | a0001 | c0002 | t0007 | g0044 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18962 | hp1 | a0001 | c0002 | t0001 | g0158 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18962 | hp2 | a0001 | c0001 | t0003 | g0234 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18963 | hp1 | a0001 | c0002 | t0034 | g0034 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18963 | hp2 | a0001 | c0001 | t0027 | g0323 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18964 | hp1 | a0001 | c0001 | t0021 | g0212 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18964 | hp2 | a0001 | c0001 | t0003 | g0208 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18966 | hp1 | a0001 | c0001 | t0010 | g0199 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18966 | hp2 | a0001 | c0002 | t0007 | g0035 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18967 | hp1 | a0001 | c0001 | t0003 | g0172 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18967 | hp2 | a0001 | c0002 | t0001 | g0095 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18969 | hp2 | a0002 | c0003 | t0018 | g0344 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18970 | hp1 | a0001 | c0001 | t0012 | g0230 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18970 | hp2 | a0002 | c0003 | t0004 | g0226 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18972 | hp1 | a0001 | c0002 | t0022 | g0116 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18973 | hp1 | a0001 | c0001 | t0021 | g0303 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18973 | hp2 | a0001 | c0001 | t0003 | g0245 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18975 | hp1 | a0002 | c0003 | t0004 | g0350 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18975 | hp2 | a0001 | c0001 | t0003 | g0209 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18977 | hp1 | a0001 | c0002 | t0001 | g0082 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18977 | hp2 | a0001 | c0001 | t0003 | g0195 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18978 | hp1 | a0002 | c0003 | t0012 | g0363 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18978 | hp2 | a0001 | c0002 | t0001 | g0163 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18979 | hp1 | a0001 | c0001 | t0003 | g0279 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18979 | hp2 | a0002 | c0003 | t0004 | g0336 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18981 | hp1 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18981 | hp2 | a0001 | c0001 | t0010 | g0165 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18982 | hp1 | a0001 | c0001 | t0025 | g0251 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18982 | hp2 | a0001 | c0002 | t0016 | g0117 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18983 | hp1 | a0001 | c0002 | t0001 | g0097 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18983 | hp2 | a0001 | c0001 | t0010 | g0197 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18985 | hp1 | a0001 | c0001 | t0003 | g0329 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18985 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18986 | hp1 | a0001 | c0002 | t0016 | g0091 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18986 | hp2 | a0001 | c0001 | t0028 | g0200 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18989 | hp1 | a0001 | c0002 | t0001 | g0056 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18989 | hp2 | a0001 | c0001 | t0003 | g0190 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18991 | hp1 | a0001 | c0002 | t0052 | g0108 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18991 | hp2 | a0001 | c0001 | t0003 | g0330 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18997 | hp1 | a0002 | c0003 | t0041 | g0365 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18997 | hp2 | a0001 | c0001 | t0010 | g0145 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18998 | hp1 | a0001 | c0002 | t0001 | g0057 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19000 | hp1 | a0002 | c0003 | t0004 | g0264 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19000 | hp2 | a0001 | c0002 | t0053 | g0046 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19001 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19001 | hp2 | a0001 | c0001 | t0035 | g0244 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19002 | hp1 | a0001 | c0001 | t0003 | g0186 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19002 | hp2 | a0002 | c0003 | t0019 | g0359 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19004 | hp1 | a0001 | c0001 | t0003 | g0255 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19005 | hp1 | a0001 | c0002 | t0007 | g0318 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19005 | hp2 | a0002 | c0003 | t0004 | g0171 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19009 | hp1 | a0001 | c0001 | t0035 | g0231 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0316 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19010 | hp1 | a0001 | c0001 | t0003 | g0280 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19010 | hp2 | a0002 | c0003 | t0012 | g0331 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19011 | hp1 | a0001 | c0002 | t0007 | g0045 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19011 | hp2 | a0001 | c0001 | t0003 | g0232 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19030 | hp1 | a0001 | c0002 | t0001 | g0076 | AFR | LWK | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19030 | hp2 | a0001 | c0001 | t0055 | g0122 | AFR | LWK | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19043 | hp1 | a0005 | c0007 | t0033 | g0048 | AFR | LWK | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19043 | hp2 | a0001 | c0001 | t0008 | g0269 | AFR | LWK | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19054 | hp1 | a0002 | c0003 | t0019 | g0367 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19054 | hp2 | a0001 | c0002 | t0007 | g0313 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19055 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19055 | hp2 | a0002 | c0003 | t0004 | g0249 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19057 | hp1 | a0001 | c0001 | t0003 | g0354 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19057 | hp2 | a0002 | c0003 | t0004 | g0083 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19058 | hp1 | a0001 | c0001 | t0036 | g0191 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19058 | hp2 | a0001 | c0002 | t0001 | g0160 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19060 | hp2 | a0001 | c0002 | t0001 | g0054 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19062 | hp1 | a0001 | c0001 | t0010 | g0187 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19062 | hp2 | a0001 | c0002 | t0001 | g0109 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19064 | hp2 | a0001 | c0001 | t0003 | g0254 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19065 | hp1 | a0001 | c0002 | t0007 | g0043 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19065 | hp2 | a0002 | c0003 | t0004 | g0351 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19067 | hp1 | a0001 | c0001 | t0010 | g0196 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19067 | hp2 | a0001 | c0002 | t0001 | g0105 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19070 | hp1 | a0001 | c0001 | t0003 | g0253 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0317 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19072 | hp1 | a0001 | c0001 | t0025 | g0229 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19072 | hp2 | a0001 | c0002 | t0007 | g0049 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19074 | hp1 | a0001 | c0001 | t0029 | g0194 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19074 | hp2 | a0002 | c0003 | t0004 | g0345 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19076 | hp1 | a0001 | c0001 | t0027 | g0272 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19076 | hp2 | a0001 | c0002 | t0001 | g0162 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19078 | hp1 | a0001 | c0001 | t0002 | g0307 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19078 | hp2 | a0001 | c0002 | t0001 | g0089 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19080 | hp1 | a0001 | c0002 | t0001 | g0107 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19080 | hp2 | a0001 | c0001 | t0003 | g0189 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19081 | hp1 | a0002 | c0003 | t0040 | g0227 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19081 | hp2 | a0010 | c0010 | t0004 | g0358 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19084 | hp1 | a0002 | c0003 | t0004 | g0337 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19084 | hp2 | a0001 | c0002 | t0058 | g0052 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19085 | hp1 | a0001 | c0002 | t0001 | g0284 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19085 | hp2 | a0002 | c0003 | t0012 | g0338 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19088 | hp1 | a0001 | c0001 | t0003 | g0182 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19088 | hp2 | a0002 | c0003 | t0004 | g0349 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19089 | hp1 | a0001 | c0001 | t0010 | g0185 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19089 | hp2 | a0001 | c0002 | t0001 | g0096 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19091 | hp1 | a0001 | c0001 | t0028 | g0198 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19091 | hp2 | a0002 | c0003 | t0004 | g0343 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19240 | hp1 | a0001 | c0001 | t0013 | g0168 | AFR | YRI | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19240 | hp2 | a0001 | c0002 | t0001 | g0061 | AFR | YRI | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA20129 | hp1 | a0001 | c0001 | t0013 | g0176 | AFR | ASW | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA20129 | hp2 | a0001 | c0002 | t0001 | g0238 | AFR | ASW | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA20752 | hp1 | a0001 | c0001 | t0009 | g0021 | EUR | TSI | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0308 | EUR | TSI | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA20805 | hp1 | a0001 | c0002 | t0001 | g0068 | EUR | TSI | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA20805 | hp2 | a0006 | c0009 | t0003 | g0228 | EUR | TSI | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA20905 | hp1 | a0002 | c0003 | t0004 | g0366 | SAS | GIH | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0085 | SAS | GIH | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0174 | AFR | ACB | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02109 | hp2 | a0003 | c0004 | t0005 | g0155 | AFR | ACB | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02486 | hp1 | a0003 | c0004 | t0032 | g0138 | AFR | ACB | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02486 | hp2 | a0001 | c0001 | t0008 | g0143 | AFR | ACB | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02559 | hp1 | a0001 | c0001 | t0021 | g0291 | AFR | ACB | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02559 | hp2 | a0001 | c0002 | t0001 | g0071 | AFR | ACB | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG03471 | hp1 | a0005 | c0007 | t0033 | g0029 | AFR | MSL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG03471 | hp2 | a0001 | c0011 | t0008 | g0224 | AFR | MSL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG06807 | hp1 | a0001 | c0001 | t0006 | g0031 | AFR | USA | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG06807 | hp2 | a0001 | c0001 | t0014 | g0001 | AFR | USA | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18955 | hp1 | a0001 | c0002 | t0001 | g0070 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18955 | hp2 | a0009 | c0014 | t0004 | g0243 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA20300 | hp1 | a0001 | c0001 | t0044 | g0164 | AFR | USA | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0216 | AFR | USA | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA21309 | hp1 | a0004 | c0006 | t0001 | g0099 | AFR | LWK | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA21309 | hp2 | a0001 | c0001 | t0003 | g0257 | AFR | LWK | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
homoSapiens_chm13v2 | hp1 | a0003 | c0004 | t0005 | g0135 | REF | REF | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0008 | REF | REF | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:82759440
|
C | T | 1 | a0003 | 22 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(19): Show |
missense_variant | MODERATE | c.2158G>A | p.Glu720Lys | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 2340/6418 | 2158/2250 | 720/749 | chr15 | 82759440 | ||
chr15:82762238
|
G | A | 1 | a0004 | 2 | HG02922.hp2 NA21309.hp1 |
missense_variant | MODERATE | c.1861C>T | p.His621Tyr | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 12/13 | 2043/6418 | 1861/2250 | 621/749 | chr15 | 82762238 | ||
chr15:82765907
|
G | A | 1 | a0005 | 2 | HG03471.hp1 NA19043.hp1 |
missense_variant | MODERATE | c.1678C>T | p.His560Tyr | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 10/13 | 1860/6418 | 1678/2250 | 560/749 | chr15 | 82765907 | ||
chr15:82765945
|
A | G | 1 | a0008 | 1 | HG00438.hp1 | missense_variant | MODERATE | c.1640T>C | p.Met547Thr | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 10/13 | 1822/6418 | 1640/2250 | 547/749 | chr15 | 82765945 | ||
chr15:82769022
|
G | A | 1 | a0009 | 1 | NA18955.hp2 | missense_variant | MODERATE | c.1411C>T | p.Pro471Ser | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 9/13 | 1593/6418 | 1411/2250 | 471/749 | chr15 | 82769022 | ||
chr15:82772084
|
G | A | 1 | a0007 | 1 | HG00735.hp2 | missense_variant | MODERATE | c.1256C>T | p.Thr419Met | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 7/13 | 1438/6418 | 1256/2250 | 419/749 | chr15 | 82772084 | ||
chr15:82778879
|
T | G | 5 | a0002a0007a0008others(2): Show | 57 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(54): Show |
missense_variant | MODERATE | c.998A>C | p.Lys333Thr | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/13 | 1180/6418 | 998/2250 | 333/749 | chr15 | 82778879 | ||
chr15:82782857
|
A | AAGTATCT others(13): Show |
1 | a0010 | 1 | NA19081.hp2 | frameshift_variant&stop_gained | HIGH | c.884_903dupGTGGAGAA others(12): Show |
p.Cys302fs | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/13 | 1085/6418 | 903/2250 | 301/749 | chr15 | 82782857 | ||
chr15:82787093
|
C | T | 1 | a0006 | 1 | NA20805.hp2 | missense_variant | MODERATE | c.298G>A | p.Val100Ile | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 2/13 | 480/6418 | 298/2250 | 100/749 | chr15 | 82787093 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:82759441
|
G | A | 3 | a0001c0002a0001c0012a0004c0006 | 95 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(92): Show |
synonymous_variant | LOW | c.2157C>T | p.His719His | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 2339/6418 | 2157/2250 | 719/749 | chr15 | 82759441 | ||
chr15:82765956
|
T | G | 1 | a0001c0012 | 1 | NA18945.hp1 | synonymous_variant | LOW | c.1629A>C | p.Arg543Arg | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 10/13 | 1811/6418 | 1629/2250 | 543/749 | chr15 | 82765956 | ||
chr15:82778842
|
T | C | 1 | a0001c0008 | 2 | HG01884.hp2 HG02965.hp1 |
synonymous_variant | LOW | c.1035A>G | p.Ala345Ala | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/13 | 1217/6418 | 1035/2250 | 345/749 | chr15 | 82778842 | ||
chr15:82782807
|
C | T | 1 | a0001c0011 | 1 | HG03471.hp2 | synonymous_variant | LOW | c.954G>A | p.Val318Val | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/13 | 1136/6418 | 954/2250 | 318/749 | chr15 | 82782807 | ||
chr15:82782948
|
C | T | 1 | a0004c0006 | 2 | HG02922.hp2 NA21309.hp1 |
synonymous_variant | LOW | c.813G>A | p.Glu271Glu | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/13 | 995/6418 | 813/2250 | 271/749 | chr15 | 82782948 | ||
chr15:82786989
|
G | A | 1 | a0001c0005 | 5 | HG00639.hp2 HG00735.hp1 HG01361.hp2 others(2): Show |
synonymous_variant | LOW | c.402C>T | p.Phe134Phe | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 2/13 | 584/6418 | 402/2250 | 134/749 | chr15 | 82786989 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:82755506
|
A | G | 1 | a0002c0003t0019 | 3 | HG02071.hp1 NA19002.hp2 NA19054.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3842T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 3842 | chr15 | 82755506 | |||||
chr15:82755563
|
A | AT | 5 | a0001c0001t0009a0001c0001t0037a0001c0001t0048others(2): Show | 12 | HG01257.hp2 HG01258.hp2 HG01361.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3784dupA | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 3784 | chr15 | 82755563 | |||||
chr15:82755563
|
AT | A | 10 | a0001c0001t0008a0001c0001t0021a0001c0001t0028others(7): Show | 22 | HG00323.hp2 HG01070.hp2 HG02055.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*3784delA | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 3784 | chr15 | 82755563 | |||||
chr15:82755944
|
T | C | 2 | a0001c0001t0013a0001c0001t0043 | 7 | HG02895.hp1 HG02965.hp2 HG02976.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3404A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 3404 | chr15 | 82755944 | |||||
chr15:82756281
|
C | T | 1 | a0001c0001t0059 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3067G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 3067 | chr15 | 82756281 | |||||
chr15:82756396
|
TAAG | T | 15 | a0001c0001t0026a0001c0002t0001a0001c0002t0007others(12): Show | 97 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*2949_*2951delCTT | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 2949 | chr15 | 82756396 | |||||
chr15:82756562
|
T | G | 3 | a0001c0001t0006a0001c0001t0009a0001c0001t0055 | 20 | HG00099.hp2 HG01106.hp1 HG01192.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*2786A>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 2786 | chr15 | 82756562 | |||||
chr15:82756567
|
G | A | 1 | a0001c0002t0056 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2781C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 2781 | chr15 | 82756567 | |||||
chr15:82756673
|
T | A | 2 | a0001c0001t0010a0001c0001t0028 | 9 | NA18966.hp1 NA18981.hp2 NA18983.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2675A>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 2675 | chr15 | 82756673 | |||||
chr15:82757118
|
A | C | 2 | a0001c0001t0008a0001c0011t0008 | 9 | HG02055.hp1 HG02451.hp2 HG02486.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2230T>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 2230 | chr15 | 82757118 | |||||
chr15:82757210
|
G | A | 1 | a0001c0001t0017 | 3 | HG03098.hp1 HG03209.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2138C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 2138 | chr15 | 82757210 | |||||
chr15:82757254
|
A | C | 1 | a0003c0004t0046 | 1 | HG00738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2094T>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 2094 | chr15 | 82757254 | |||||
chr15:82757351
|
C | CT | 23 | a0001c0001t0006a0001c0001t0009a0001c0001t0013others(20): Show | 131 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(128): Show |
3_prime_UTR_variant | MODIFIER | c.*1996dupA | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 1996 | chr15 | 82757351 | |||||
chr15:82757351
|
C | CTT | 4 | a0001c0001t0055a0001c0002t0022a0001c0002t0054others(1): Show | 6 | HG01109.hp1 HG01952.hp1 HG04184.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1995_*1996dupAA | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 1996 | chr15 | 82757351 | |||||
chr15:82757351
|
CT | C | 32 | a0001c0001t0003a0001c0001t0008a0001c0001t0010others(29): Show | 163 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(160): Show |
3_prime_UTR_variant | MODIFIER | c.*1996delA | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 1996 | chr15 | 82757351 | |||||
chr15:82757457
|
G | A | 1 | a0001c0001t0044 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1891C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 1891 | chr15 | 82757457 | |||||
chr15:82757477
|
G | A | 1 | a0002c0003t0040 | 1 | NA19081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1871C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 1871 | chr15 | 82757477 | |||||
chr15:82757480
|
C | T | 1 | a0002c0003t0040 | 1 | NA19081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1868G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 1868 | chr15 | 82757480 | |||||
chr15:82757483
|
C | T | 3 | a0001c0002t0007a0001c0002t0034a0001c0002t0053 | 13 | HG00423.hp1 HG00673.hp1 HG02165.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1865G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 1865 | chr15 | 82757483 | |||||
chr15:82757498
|
A | AT | 8 | a0001c0001t0031a0003c0004t0005a0003c0004t0020others(5): Show | 22 | HG00738.hp2 HG00741.hp1 HG01074.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1849dupA | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 1849 | chr15 | 82757498 | |||||
chr15:82757504
|
T | TA | 1 | a0001c0001t0015 | 4 | HG02257.hp1 HG02572.hp1 HG03041.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1843_*1844insT | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 1843 | chr15 | 82757504 | |||||
chr15:82757534
|
G | A | 1 | a0003c0004t0050 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1814C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 1814 | chr15 | 82757534 | |||||
chr15:82757589
|
C | T | 2 | a0003c0004t0020a0003c0004t0045 | 4 | HG00741.hp1 HG01074.hp2 HG01515.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1759G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 1759 | chr15 | 82757589 | |||||
chr15:82757590
|
C | G | 2 | a0001c0001t0036a0001c0002t0052 | 2 | NA18991.hp1 NA19058.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1758G>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 1758 | chr15 | 82757590 | |||||
chr15:82757628
|
G | A | 2 | a0001c0002t0057a0001c0002t0058 | 2 | NA18947.hp1 NA19084.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1720C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 1720 | chr15 | 82757628 | |||||
chr15:82757767
|
G | A | 1 | a0005c0007t0033 | 2 | HG03471.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1581C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 1581 | chr15 | 82757767 | |||||
chr15:82757858
|
T | C | 1 | a0001c0001t0051 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1490A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 1490 | chr15 | 82757858 | |||||
chr15:82757893
|
T | C | 27 | a0001c0001t0006a0001c0001t0009a0001c0001t0013others(24): Show | 138 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(135): Show |
3_prime_UTR_variant | MODIFIER | c.*1455A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 1455 | chr15 | 82757893 | |||||
chr15:82757975
|
A | G | 6 | a0001c0001t0013a0001c0001t0015a0001c0001t0030others(3): Show | 16 | HG02257.hp1 HG02572.hp1 HG02895.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1373T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 1373 | chr15 | 82757975 | |||||
chr15:82758027
|
A | G | 1 | a0001c0001t0014 | 4 | HG02809.hp2 HG03195.hp2 HG06807.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1321T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 1321 | chr15 | 82758027 | |||||
chr15:82758047
|
T | A | 1 | a0001c0001t0059 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1301A>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 1301 | chr15 | 82758047 | |||||
chr15:82758050
|
C | T | 1 | a0001c0001t0014 | 4 | HG02809.hp2 HG03195.hp2 HG06807.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1298G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 1298 | chr15 | 82758050 | |||||
chr15:82758070
|
C | T | 4 | a0001c0001t0012a0002c0003t0012a0002c0003t0038others(1): Show | 8 | HG00280.hp1 HG01975.hp1 HG02132.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1278G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 1278 | chr15 | 82758070 | |||||
chr15:82758080
|
T | C | 1 | a0001c0002t0060 | 1 | HG01975.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1268A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 1268 | chr15 | 82758080 | |||||
chr15:82758099
|
C | T | 1 | a0001c0001t0042 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1249G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 1249 | chr15 | 82758099 | |||||
chr15:82758191
|
A | T | 2 | a0001c0001t0025a0001c0001t0035 | 4 | NA18982.hp1 NA19001.hp2 NA19009.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1157T>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 1157 | chr15 | 82758191 | |||||
chr15:82758268
|
A | G | 13 | a0001c0001t0012a0002c0003t0004a0002c0003t0012others(10): Show | 58 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*1080T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 1080 | chr15 | 82758268 | |||||
chr15:82758353
|
C | T | 1 | a0002c0003t0038 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*995G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 995 | chr15 | 82758353 | |||||
chr15:82758479
|
A | C | 2 | a0001c0001t0008a0001c0011t0008 | 9 | HG02055.hp1 HG02451.hp2 HG02486.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*869T>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 869 | chr15 | 82758479 | |||||
chr15:82758642
|
T | C | 12 | a0001c0001t0003a0001c0001t0010a0001c0001t0017others(9): Show | 80 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*706A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 706 | chr15 | 82758642 | |||||
chr15:82758709
|
A | G | 1 | a0001c0001t0030 | 2 | HG03486.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*639T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 639 | chr15 | 82758709 | |||||
chr15:82758932
|
C | T | 12 | a0001c0001t0003a0001c0001t0010a0001c0001t0017others(9): Show | 80 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*416G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 416 | chr15 | 82758932 | |||||
chr15:82759066
|
G | A | 1 | a0001c0001t0035 | 2 | NA19001.hp2 NA19009.hp1 |
3_prime_UTR_variant | MODIFIER | c.*282C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 282 | chr15 | 82759066 | |||||
chr15:82806030
|
T | C | 1 | a0001c0001t0024 | 3 | HG01070.hp1 HG01071.hp2 HG01261.hp2 |
5_prime_UTR_variant | MODIFIER | c.-143A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/13 | 18640 | chr15 | 82806030 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:82759689
|
C | T | 1 | a0002c0003t0004g0370 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1998-89G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 12/12 | chr15 | 82759689 | ||||||
chr15:82759738
|
CATTTCTA others(5): Show |
C | 2 | a0001c0001t0002g0309a0001c0001t0002g0310 | 2 | HG00738.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.1998-150_1998-139d others(14): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 12/12 | chr15 | 82759738 | ||||||
chr15:82759800
|
C | CT | 37 | a0001c0001t0013g0167a0001c0001t0013g0168a0001c0001t0013g0176others(34): Show | 38 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.1998-201dupA | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 12/12 | chr15 | 82759800 | ||||||
chr15:82759816
|
T | C | 325 | a0001c0001t0002g0084a0001c0001t0002g0085a0001c0001t0002g0121others(322): Show | 332 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(329): Show |
intron_variant | MODIFIER | c.1998-216A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 12/12 | chr15 | 82759816 | ||||||
chr15:82759960
|
A | AT | 57 | a0001c0001t0012g0230a0002c0003t0004g0004a0002c0003t0004g0083others(54): Show | 58 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.1998-361dupA | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 12/12 | chr15 | 82759960 | ||||||
chr15:82759990
|
C | T | 4 | a0001c0005t0011g0006a0001c0005t0011g0371a0001c0005t0011g0372others(1): Show | 5 | HG00639.hp2 HG00735.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.1998-390G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 12/12 | chr15 | 82759990 | ||||||
chr15:82760090
|
G | A | 1 | a0001c0001t0044g0164 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1998-490C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 12/12 | chr15 | 82760090 | ||||||
chr15:82760103
|
T | C | 3 | a0001c0001t0024g0374a0001c0001t0024g0375a0001c0001t0024g0376 | 3 | HG01070.hp1 HG01071.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.1998-503A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 12/12 | chr15 | 82760103 | ||||||
chr15:82760173
|
T | G | 57 | a0001c0001t0012g0230a0002c0003t0004g0004a0002c0003t0004g0083others(54): Show | 58 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.1998-573A>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 12/12 | chr15 | 82760173 | ||||||
chr15:82760391
|
A | T | 1 | a0001c0002t0001g0012 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1998-791T>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 12/12 | chr15 | 82760391 | ||||||
chr15:82760592
|
C | CTA | 326 | a0001c0001t0002g0084a0001c0001t0002g0085a0001c0001t0002g0121others(323): Show | 333 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(330): Show |
intron_variant | MODIFIER | c.1998-994_1998-993d others(4): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 12/12 | chr15 | 82760592 | ||||||
chr15:82760723
|
A | G | 326 | a0001c0001t0002g0084a0001c0001t0002g0085a0001c0001t0002g0121others(323): Show | 333 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(330): Show |
intron_variant | MODIFIER | c.1998-1123T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 12/12 | chr15 | 82760723 | ||||||
chr15:82760739
|
G | GCA | 218 | a0001c0001t0002g0121a0001c0001t0002g0296a0001c0001t0002g0320others(215): Show | 220 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.1998-1141_1998-114 others(6): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 12/12 | chr15 | 82760739 | ||||||
chr15:82760739
|
G | GCACA | 79 | a0001c0001t0003g0182a0001c0001t0003g0189a0001c0001t0003g0201others(76): Show | 80 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.1998-1143_1998-114 others(8): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 12/12 | chr15 | 82760739 | ||||||
chr15:82760739
|
G | GCACACA | 6 | a0001c0001t0013g0168a0001c0001t0013g0176a0001c0001t0013g0178others(3): Show | 6 | HG02965.hp2 HG02976.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1998-1145_1998-114 others(10): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 12/12 | chr15 | 82760739 | ||||||
chr15:82760739
|
GCA | G | 5 | a0001c0001t0014g0001a0001c0005t0011g0006a0001c0005t0011g0371others(2): Show | 9 | HG00639.hp2 HG00735.hp1 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.1998-1141_1998-114 others(6): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 12/12 | chr15 | 82760739 | ||||||
chr15:82761024
|
T | C | 3 | a0003c0004t0005g0132a0003c0004t0005g0133a0003c0004t0005g0135 | 3 | HG01258.hp1 HG01358.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1997+1078A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 12/12 | chr15 | 82761024 | ||||||
chr15:82761103
|
G | A | 2 | a0001c0001t0013g0178a0001c0001t0013g0324 | 2 | HG02965.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1997+999C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 12/12 | chr15 | 82761103 | ||||||
chr15:82761357
|
T | C | 1 | a0001c0002t0001g0157 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1997+745A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 12/12 | chr15 | 82761357 | ||||||
chr15:82761644
|
T | C | 91 | a0001c0002t0001g0002a0001c0002t0001g0012a0001c0002t0001g0013others(88): Show | 92 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.1997+458A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 12/12 | chr15 | 82761644 | ||||||
chr15:82761659
|
A | C | 6 | a0001c0001t0003g0169a0001c0001t0003g0257a0001c0001t0003g0258others(3): Show | 6 | HG02451.hp1 HG02818.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1997+443T>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 12/12 | chr15 | 82761659 | ||||||
chr15:82761688
|
T | A | 66 | a0001c0001t0002g0174a0001c0001t0002g0175a0001c0001t0012g0230others(63): Show | 67 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.1997+414A>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 12/12 | chr15 | 82761688 | ||||||
chr15:82761738
|
A | G | 1 | a0001c0001t0044g0164 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1997+364T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 12/12 | chr15 | 82761738 | ||||||
chr15:82761921
|
G | C | 61 | a0001c0001t0012g0230a0001c0005t0011g0006a0001c0005t0011g0371others(58): Show | 63 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.1997+181C>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 12/12 | chr15 | 82761921 | ||||||
chr15:82762520
|
A | G | 57 | a0001c0001t0012g0230a0002c0003t0004g0004a0002c0003t0004g0083others(54): Show | 58 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.1821-242T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 11/12 | chr15 | 82762520 | ||||||
chr15:82762700
|
A | G | 67 | a0001c0001t0012g0230a0001c0002t0001g0037a0001c0002t0001g0073others(64): Show | 69 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.1821-422T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 11/12 | chr15 | 82762700 | ||||||
chr15:82762907
|
C | T | 3 | a0001c0001t0002g0087a0001c0001t0002g0276a0001c0001t0002g0311 | 3 | HG01952.hp2 HG02735.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1821-629G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 11/12 | chr15 | 82762907 | ||||||
chr15:82762972
|
A | G | 1 | a0002c0003t0004g0366 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1821-694T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 11/12 | chr15 | 82762972 | ||||||
chr15:82763153
|
T | A | 57 | a0001c0001t0012g0230a0002c0003t0004g0004a0002c0003t0004g0083others(54): Show | 58 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.1821-875A>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 11/12 | chr15 | 82763153 | ||||||
chr15:82763321
|
T | C | 1 | a0002c0003t0004g0350 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1821-1043A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 11/12 | chr15 | 82763321 | ||||||
chr15:82763415
|
A | G | 1 | a0001c0002t0001g0102 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1821-1137T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 11/12 | chr15 | 82763415 | ||||||
chr15:82763675
|
C | CTT | 198 | a0001c0001t0002g0087a0001c0001t0006g0016a0001c0001t0006g0017others(195): Show | 201 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.1821-1398_1821-139 others(6): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 11/12 | chr15 | 82763675 | ||||||
chr15:82763677
|
G | C | 1 | a0001c0001t0002g0311 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1821-1399C>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 11/12 | chr15 | 82763677 | ||||||
chr15:82763897
|
G | A | 10 | a0001c0001t0008g0143a0001c0001t0008g0214a0001c0001t0008g0215others(7): Show | 10 | HG01891.hp1 HG02055.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1820+1269C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 11/12 | chr15 | 82763897 | ||||||
chr15:82763942
|
G | A | 1 | a0001c0001t0003g0026 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1820+1224C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 11/12 | chr15 | 82763942 | ||||||
chr15:82764449
|
G | A | 3 | a0001c0001t0008g0214a0001c0001t0008g0215a0001c0001t0008g0239 | 3 | HG02055.hp1 HG02451.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1820+717C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 11/12 | chr15 | 82764449 | ||||||
chr15:82764462
|
C | T | 14 | a0003c0004t0005g0003a0003c0004t0005g0010a0003c0004t0005g0126others(11): Show | 15 | HG00323.hp2 HG00738.hp2 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.1820+704G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 11/12 | chr15 | 82764462 | ||||||
chr15:82764492
|
C | CT | 15 | a0001c0001t0002g0036a0001c0001t0002g0087a0001c0001t0002g0297others(12): Show | 16 | HG00323.hp1 HG00597.hp1 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.1820+673dupA | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 11/12 | chr15 | 82764492 | ||||||
chr15:82764492
|
C | CTT | 7 | a0001c0001t0015g0219a0001c0001t0015g0220a0001c0001t0015g0221others(4): Show | 7 | HG01243.hp2 HG02257.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1820+672_1820+673d others(4): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 11/12 | chr15 | 82764492 | ||||||
chr15:82764492
|
C | CTTTTTTT others(2): Show |
6 | a0002c0003t0004g0335a0002c0003t0004g0339a0002c0003t0004g0343others(3): Show | 6 | HG01975.hp1 HG01993.hp1 HG02015.hp2 others(3): Show |
intron_variant | MODIFIER | c.1820+665_1820+673d others(11): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 11/12 | chr15 | 82764492 | ||||||
chr15:82764492
|
C | CTTTTTTT others(3): Show |
34 | a0002c0003t0004g0004a0002c0003t0004g0083a0002c0003t0004g0111others(31): Show | 35 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(32): Show |
intron_variant | MODIFIER | c.1820+664_1820+673d others(12): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 11/12 | chr15 | 82764492 | ||||||
chr15:82764492
|
C | CTTTTTTT others(4): Show |
13 | a0001c0001t0012g0230a0002c0003t0004g0171a0002c0003t0004g0226others(10): Show | 13 | HG00423.hp2 HG01175.hp2 HG01978.hp2 others(10): Show |
intron_variant | MODIFIER | c.1820+663_1820+673d others(13): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 11/12 | chr15 | 82764492 | ||||||
chr15:82764492
|
C | CTTTTTTT others(5): Show |
6 | a0001c0001t0013g0167a0001c0001t0013g0168a0001c0001t0043g0166others(3): Show | 6 | HG02895.hp1 HG03139.hp2 HG03654.hp2 others(3): Show |
intron_variant | MODIFIER | c.1820+662_1820+673d others(14): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 11/12 | chr15 | 82764492 | ||||||
chr15:82764492
|
C | CTTTTTTT others(8): Show |
1 | a0002c0003t0041g0365 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1820+659_1820+673d others(17): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 11/12 | chr15 | 82764492 | ||||||
chr15:82764492
|
C | CTTTTTTT others(9): Show |
3 | a0001c0002t0001g0101a0001c0002t0034g0034a0001c0002t0056g0103 | 3 | HG03041.hp2 HG03453.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.1820+658_1820+673d others(18): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 11/12 | chr15 | 82764492 | ||||||
chr15:82764492
|
C | CTTTTTTT others(10): Show |
13 | a0001c0002t0001g0030a0001c0002t0001g0037a0001c0002t0001g0054others(10): Show | 13 | HG01943.hp1 HG02074.hp2 HG03139.hp1 others(10): Show |
intron_variant | MODIFIER | c.1820+657_1820+673d others(19): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 11/12 | chr15 | 82764492 | ||||||
chr15:82764492
|
C | CTTTTTTT others(11): Show |
25 | a0001c0001t0009g0023a0001c0001t0030g0289a0001c0001t0042g0033others(22): Show | 25 | HG00639.hp1 HG00673.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.1820+656_1820+673d others(20): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 11/12 | chr15 | 82764492 | ||||||
chr15:82764492
|
C | CTTTTTTT others(12): Show |
21 | a0001c0001t0006g0017a0001c0001t0006g0024a0001c0001t0006g0120others(18): Show | 21 | HG00140.hp1 HG01106.hp1 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.1820+655_1820+673d others(21): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 11/12 | chr15 | 82764492 | ||||||
chr15:82764492
|
C | CTTTTTTT others(13): Show |
12 | a0001c0001t0006g0019a0001c0001t0006g0025a0001c0001t0006g0027others(9): Show | 12 | HG00099.hp2 HG01346.hp2 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.1820+654_1820+673d others(22): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 11/12 | chr15 | 82764492 | ||||||
chr15:82764492
|
C | CTTTTTTT others(14): Show |
2 | a0001c0001t0006g0016a0001c0001t0009g0022 | 2 | HG01192.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.1820+673_1820+674i others(23): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 11/12 | chr15 | 82764492 | ||||||
chr15:82764492
|
C | CTTTTTTT others(16): Show |
1 | a0005c0007t0033g0048 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1820+673_1820+674i others(25): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 11/12 | chr15 | 82764492 | ||||||
chr15:82764492
|
C | CTTTTTTT others(19): Show |
1 | a0001c0001t0013g0282 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1820+673_1820+674i others(28): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 11/12 | chr15 | 82764492 | ||||||
chr15:82764492
|
C | CTTTTTTT others(25): Show |
1 | a0001c0001t0013g0176 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1820+673_1820+674i others(34): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 11/12 | chr15 | 82764492 | ||||||
chr15:82764492
|
CTTTT | C | 109 | a0001c0001t0003g0014a0001c0001t0003g0015a0001c0001t0003g0026others(106): Show | 113 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.1820+670_1820+673d others(6): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 11/12 | chr15 | 82764492 | ||||||
chr15:82764767
|
C | T | 1 | a0001c0001t0003g0182 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1820+399G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 11/12 | chr15 | 82764767 | ||||||
chr15:82764815
|
T | C | 2 | a0001c0008t0023g0286a0001c0008t0023g0287 | 2 | HG01884.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1820+351A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 11/12 | chr15 | 82764815 | ||||||
chr15:82764817
|
G | T | 6 | a0001c0001t0015g0219a0001c0001t0015g0220a0001c0001t0015g0221others(3): Show | 6 | HG02257.hp1 HG02572.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1820+349C>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 11/12 | chr15 | 82764817 | ||||||
chr15:82764956
|
C | A | 92 | a0001c0001t0002g0087a0001c0002t0001g0002a0001c0002t0001g0012others(89): Show | 93 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.1820+210G>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 11/12 | chr15 | 82764956 | ||||||
chr15:82765026
|
A | G | 134 | a0001c0001t0002g0087a0001c0001t0006g0016a0001c0001t0006g0017others(131): Show | 135 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.1820+140T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 11/12 | chr15 | 82765026 | ||||||
chr15:82765443
|
A | G | 1 | a0001c0001t0059g0124 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1688-145T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 10/12 | chr15 | 82765443 | ||||||
chr15:82765497
|
C | A | 3 | a0001c0001t0024g0374a0001c0001t0024g0375a0001c0001t0024g0376 | 3 | HG01070.hp1 HG01071.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.1688-199G>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 10/12 | chr15 | 82765497 | ||||||
chr15:82765658
|
G | A | 198 | a0001c0001t0002g0087a0001c0001t0006g0016a0001c0001t0006g0017others(195): Show | 201 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.1687+240C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 10/12 | chr15 | 82765658 | ||||||
chr15:82765749
|
G | A | 137 | a0001c0001t0002g0087a0001c0001t0006g0016a0001c0001t0006g0017others(134): Show | 138 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.1687+149C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 10/12 | chr15 | 82765749 | ||||||
chr15:82765834
|
G | T | 1 | a0001c0012t0001g0064 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1687+64C>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 10/12 | chr15 | 82765834 | ||||||
chr15:82766336
|
A | C | 1 | a0001c0001t0014g0001 | 4 | HG02809.hp2 HG03195.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1554-305T>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 9/12 | chr15 | 82766336 | ||||||
chr15:82766394
|
C | T | 1 | a0001c0001t0042g0033 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1554-363G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 9/12 | chr15 | 82766394 | ||||||
chr15:82766451
|
C | T | 2 | a0005c0007t0033g0029a0005c0007t0033g0048 | 2 | HG03471.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1554-420G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 9/12 | chr15 | 82766451 | ||||||
chr15:82766456
|
A | G | 1 | a0001c0001t0014g0001 | 4 | HG02809.hp2 HG03195.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1554-425T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 9/12 | chr15 | 82766456 | ||||||
chr15:82766512
|
C | T | 6 | a0001c0002t0001g0051a0001c0002t0001g0059a0001c0002t0001g0065others(3): Show | 6 | HG00140.hp1 HG00639.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1554-481G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 9/12 | chr15 | 82766512 | ||||||
chr15:82766558
|
A | T | 10 | a0001c0002t0001g0012a0001c0002t0001g0077a0001c0002t0001g0078others(7): Show | 10 | HG00609.hp1 HG01975.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.1554-527T>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 9/12 | chr15 | 82766558 | ||||||
chr15:82766688
|
A | G | 3 | a0001c0002t0001g0106a0001c0002t0001g0113a0001c0002t0001g0247 | 3 | HG01243.hp2 HG02055.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.1554-657T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 9/12 | chr15 | 82766688 | ||||||
chr15:82766738
|
C | CA | 57 | a0001c0001t0003g0172a0001c0001t0010g0196a0001c0001t0012g0230others(54): Show | 58 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.1554-708dupT | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 9/12 | chr15 | 82766738 | ||||||
chr15:82766738
|
CA | C | 99 | a0001c0001t0002g0087a0001c0001t0002g0309a0001c0001t0006g0017others(96): Show | 100 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.1554-708delT | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 9/12 | chr15 | 82766738 | ||||||
chr15:82766755
|
A | G | 6 | a0001c0001t0003g0140a0001c0001t0003g0141a0001c0001t0003g0202others(3): Show | 6 | HG00741.hp2 HG01069.hp2 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.1554-724T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 9/12 | chr15 | 82766755 | ||||||
chr15:82766821
|
C | T | 1 | a0001c0001t0006g0016 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1554-790G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 9/12 | chr15 | 82766821 | ||||||
chr15:82766915
|
G | A | 1 | a0002c0003t0018g0357 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1554-884C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 9/12 | chr15 | 82766915 | ||||||
chr15:82767076
|
G | A | 327 | a0001c0001t0002g0084a0001c0001t0002g0085a0001c0001t0002g0087others(324): Show | 334 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(331): Show |
intron_variant | MODIFIER | c.1554-1045C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 9/12 | chr15 | 82767076 | ||||||
chr15:82767235
|
T | C | 197 | a0001c0001t0002g0087a0001c0001t0006g0016a0001c0001t0006g0017others(194): Show | 200 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.1554-1204A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 9/12 | chr15 | 82767235 | ||||||
chr15:82767303
|
A | T | 1 | a0001c0001t0002g0274 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1554-1272T>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 9/12 | chr15 | 82767303 | ||||||
chr15:82767458
|
T | C | 2 | a0001c0008t0023g0286a0001c0008t0023g0287 | 2 | HG01884.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1553+1422A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 9/12 | chr15 | 82767458 | ||||||
chr15:82767497
|
T | C | 1 | a0001c0002t0007g0043 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1553+1383A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 9/12 | chr15 | 82767497 | ||||||
chr15:82767602
|
C | A | 4 | a0001c0001t0002g0292a0001c0001t0002g0293a0001c0001t0002g0295others(1): Show | 4 | HG00733.hp1 HG01175.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.1553+1278G>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 9/12 | chr15 | 82767602 | ||||||
chr15:82767830
|
G | A | 3 | a0001c0001t0024g0374a0001c0001t0024g0375a0001c0001t0024g0376 | 3 | HG01070.hp1 HG01071.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.1553+1050C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 9/12 | chr15 | 82767830 | ||||||
chr15:82767928
|
C | T | 1 | a0001c0001t0059g0124 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1553+952G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 9/12 | chr15 | 82767928 | ||||||
chr15:82767933
|
C | T | 135 | a0001c0001t0006g0016a0001c0001t0006g0017a0001c0001t0006g0019others(132): Show | 136 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.1553+947G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 9/12 | chr15 | 82767933 | ||||||
chr15:82768465
|
A | G | 1 | a0001c0002t0001g0037 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1553+415T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 9/12 | chr15 | 82768465 | ||||||
chr15:82768483
|
C | T | 1 | a0001c0001t0003g0329 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1553+397G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 9/12 | chr15 | 82768483 | ||||||
chr15:82768594
|
T | TTGAA | 121 | a0001c0001t0002g0121a0001c0001t0002g0322a0001c0001t0006g0016others(118): Show | 121 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.1553+282_1553+285d others(6): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 9/12 | chr15 | 82768594 | ||||||
chr15:82768594
|
T | TTGAATGA others(1): Show |
3 | a0001c0001t0006g0213a0001c0002t0001g0076a0001c0002t0001g0161 | 3 | HG03130.hp2 NA18906.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1553+278_1553+285d others(10): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 9/12 | chr15 | 82768594 | ||||||
chr15:82769041
|
G | C | 1 | a0001c0001t0002g0039 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1403-11C>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 8/12 | chr15 | 82769041 | ||||||
chr15:82769288
|
G | A | 2 | a0002c0003t0004g0222a0002c0003t0004g0341 | 2 | HG00544.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.1403-258C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 8/12 | chr15 | 82769288 | ||||||
chr15:82769415
|
C | CA | 11 | a0001c0001t0003g0014a0001c0001t0003g0170a0001c0001t0003g0173others(8): Show | 12 | HG00140.hp2 HG00323.hp2 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.1402+334dupT | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 8/12 | chr15 | 82769415 | ||||||
chr15:82769415
|
CA | C | 102 | a0001c0001t0006g0017a0001c0001t0006g0019a0001c0001t0006g0024others(99): Show | 104 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.1402+334delT | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 8/12 | chr15 | 82769415 | ||||||
chr15:82769504
|
G | A | 1 | a0001c0001t0014g0001 | 4 | HG02809.hp2 HG03195.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1402+246C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 8/12 | chr15 | 82769504 | ||||||
chr15:82769565
|
C | CA | 29 | a0001c0001t0002g0174a0001c0001t0002g0175a0001c0001t0002g0216others(26): Show | 29 | HG00099.hp2 HG01106.hp1 HG01192.hp2 others(26): Show |
intron_variant | MODIFIER | c.1402+184dupT | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 8/12 | chr15 | 82769565 | ||||||
chr15:82769639
|
G | A | 1 | a0001c0001t0059g0124 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1402+111C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 8/12 | chr15 | 82769639 | ||||||
chr15:82769693
|
T | G | 1 | a0001c0001t0002g0121 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1402+57A>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 8/12 | chr15 | 82769693 | ||||||
chr15:82769925
|
G | A | 1 | a0001c0001t0002g0295 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1268-41C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 7/12 | chr15 | 82769925 | ||||||
chr15:82769951
|
G | A | 1 | a0001c0001t0010g0196 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1268-67C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 7/12 | chr15 | 82769951 | ||||||
chr15:82770126
|
G | T | 20 | a0001c0001t0006g0016a0001c0001t0006g0017a0001c0001t0006g0019others(17): Show | 20 | HG00099.hp2 HG01106.hp1 HG01192.hp2 others(17): Show |
intron_variant | MODIFIER | c.1268-242C>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 7/12 | chr15 | 82770126 | ||||||
chr15:82770181
|
G | A | 1 | a0001c0001t0006g0019 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1268-297C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 7/12 | chr15 | 82770181 | ||||||
chr15:82770275
|
C | T | 2 | a0005c0007t0033g0029a0005c0007t0033g0048 | 2 | HG03471.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1268-391G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 7/12 | chr15 | 82770275 | ||||||
chr15:82770325
|
G | A | 3 | a0001c0001t0024g0374a0001c0001t0024g0375a0001c0001t0024g0376 | 3 | HG01070.hp1 HG01071.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.1268-441C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 7/12 | chr15 | 82770325 | ||||||
chr15:82770331
|
T | C | 318 | a0001c0001t0002g0121a0001c0001t0002g0174a0001c0001t0002g0175others(315): Show | 325 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(322): Show |
intron_variant | MODIFIER | c.1268-447A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 7/12 | chr15 | 82770331 | ||||||
chr15:82770571
|
C | T | 1 | a0001c0002t0001g0082 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1268-687G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 7/12 | chr15 | 82770571 | ||||||
chr15:82770735
|
T | TG | 91 | a0001c0002t0001g0002a0001c0002t0001g0012a0001c0002t0001g0013others(88): Show | 92 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.1268-852dupC | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 7/12 | chr15 | 82770735 | ||||||
chr15:82770752
|
T | C | 1 | a0002c0003t0004g0328 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1268-868A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 7/12 | chr15 | 82770752 | ||||||
chr15:82770767
|
A | G | 318 | a0001c0001t0002g0121a0001c0001t0002g0174a0001c0001t0002g0175others(315): Show | 325 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(322): Show |
intron_variant | MODIFIER | c.1268-883T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 7/12 | chr15 | 82770767 | ||||||
chr15:82770904
|
A | G | 1 | a0001c0001t0014g0001 | 4 | HG02809.hp2 HG03195.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1268-1020T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 7/12 | chr15 | 82770904 | ||||||
chr15:82770928
|
G | T | 2 | a0001c0001t0002g0299a0001c0001t0002g0322 | 2 | HG03492.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1268-1044C>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 7/12 | chr15 | 82770928 | ||||||
chr15:82771065
|
C | T | 4 | a0001c0001t0003g0190a0001c0001t0003g0193a0001c0001t0003g0209others(1): Show | 4 | NA18951.hp2 NA18975.hp2 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.1267+1008G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 7/12 | chr15 | 82771065 | ||||||
chr15:82771263
|
T | G | 2 | a0003c0004t0020g0223a0003c0004t0045g0142 | 2 | HG00741.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.1267+810A>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 7/12 | chr15 | 82771263 | ||||||
chr15:82771274
|
C | G | 195 | a0001c0001t0006g0016a0001c0001t0006g0017a0001c0001t0006g0019others(192): Show | 198 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.1267+799G>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 7/12 | chr15 | 82771274 | ||||||
chr15:82771592
|
C | T | 195 | a0001c0001t0006g0016a0001c0001t0006g0017a0001c0001t0006g0019others(192): Show | 198 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.1267+481G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 7/12 | chr15 | 82771592 | ||||||
chr15:82771735
|
A | T | 135 | a0001c0001t0006g0016a0001c0001t0006g0017a0001c0001t0006g0019others(132): Show | 136 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.1267+338T>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 7/12 | chr15 | 82771735 | ||||||
chr15:82772058
|
C | T | 2 | a0001c0001t0002g0237a0001c0001t0021g0212 | 2 | NA18964.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.1267+15G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 7/12 | chr15 | 82772058 | ||||||
chr15:82772260
|
C | A | 58 | a0001c0001t0003g0245a0001c0001t0003g0259a0002c0003t0004g0004others(55): Show | 59 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.1112-32G>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82772260 | ||||||
chr15:82772297
|
C | G | 2 | a0001c0001t0009g0021a0001c0001t0009g0022 | 2 | HG01361.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1112-69G>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82772297 | ||||||
chr15:82772313
|
C | T | 1 | a0001c0002t0001g0079 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1112-85G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82772313 | ||||||
chr15:82772356
|
A | C | 1 | a0001c0002t0001g0054 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1112-128T>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82772356 | ||||||
chr15:82772389
|
C | T | 1 | a0002c0003t0004g0353 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1112-161G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82772389 | ||||||
chr15:82772417
|
A | G | 1 | a0001c0001t0006g0016 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1112-189T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82772417 | ||||||
chr15:82772551
|
C | A | 1 | a0001c0001t0025g0229 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1112-323G>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82772551 | ||||||
chr15:82772591
|
C | G | 184 | a0001c0001t0003g0261a0001c0001t0003g0262a0001c0001t0006g0016others(181): Show | 190 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.1112-363G>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82772591 | ||||||
chr15:82772752
|
T | C | 1 | a0001c0001t0025g0229 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1112-524A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82772752 | ||||||
chr15:82772761
|
G | A | 2 | a0001c0001t0013g0178a0001c0001t0013g0324 | 2 | HG02965.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1112-533C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82772761 | ||||||
chr15:82773047
|
A | T | 1 | a0001c0001t0012g0230 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1112-819T>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82773047 | ||||||
chr15:82773057
|
C | T | 1 | a0002c0003t0018g0357 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1112-829G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82773057 | ||||||
chr15:82773096
|
C | T | 1 | a0001c0001t0003g0140 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1112-868G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82773096 | ||||||
chr15:82773143
|
C | T | 1 | a0002c0003t0004g0349 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1112-915G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82773143 | ||||||
chr15:82773287
|
T | A | 1 | a0001c0002t0053g0046 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1112-1059A>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82773287 | ||||||
chr15:82773289
|
G | C | 12 | a0001c0001t0013g0167a0001c0001t0013g0168a0001c0001t0013g0176others(9): Show | 12 | HG02717.hp1 HG02895.hp1 HG02965.hp2 others(9): Show |
intron_variant | MODIFIER | c.1112-1061C>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82773289 | ||||||
chr15:82773315
|
G | A | 189 | a0001c0001t0006g0016a0001c0001t0006g0017a0001c0001t0006g0019others(186): Show | 192 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.1112-1087C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82773315 | ||||||
chr15:82773439
|
A | C | 10 | a0001c0001t0008g0143a0001c0001t0008g0214a0001c0001t0008g0215others(7): Show | 10 | HG01891.hp1 HG02055.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1112-1211T>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82773439 | ||||||
chr15:82773597
|
A | G | 10 | a0001c0001t0008g0143a0001c0001t0008g0214a0001c0001t0008g0215others(7): Show | 10 | HG01891.hp1 HG02055.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1112-1369T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82773597 | ||||||
chr15:82773701
|
C | A | 1 | a0002c0003t0004g0083 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1112-1473G>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82773701 | ||||||
chr15:82774247
|
G | A | 1 | a0001c0001t0003g0181 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1112-2019C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82774247 | ||||||
chr15:82774365
|
C | A | 2 | a0004c0006t0001g0099a0004c0006t0001g0100 | 2 | HG02922.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1112-2137G>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82774365 | ||||||
chr15:82774421
|
T | C | 1 | a0001c0002t0001g0283 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1112-2193A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82774421 | ||||||
chr15:82774616
|
C | A | 1 | a0002c0003t0004g0340 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1112-2388G>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82774616 | ||||||
chr15:82774656
|
C | A | 1 | a0001c0001t0002g0149 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1112-2428G>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82774656 | ||||||
chr15:82774719
|
C | CT | 9 | a0001c0001t0014g0001a0001c0002t0001g0105a0001c0008t0023g0286others(6): Show | 12 | HG00323.hp2 HG00738.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1112-2492dupA | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82774719 | ||||||
chr15:82774791
|
G | A | 2 | a0003c0004t0005g0154a0003c0004t0005g0155 | 2 | HG02109.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1112-2563C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82774791 | ||||||
chr15:82774847
|
G | A | 4 | a0001c0005t0011g0006a0001c0005t0011g0371a0001c0005t0011g0372others(1): Show | 5 | HG00639.hp2 HG00735.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.1112-2619C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82774847 | ||||||
chr15:82775039
|
A | T | 1 | a0001c0001t0008g0214 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1112-2811T>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82775039 | ||||||
chr15:82775089
|
G | A | 55 | a0002c0003t0004g0004a0002c0003t0004g0083a0002c0003t0004g0111others(52): Show | 56 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.1112-2861C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82775089 | ||||||
chr15:82775136
|
C | T | 4 | a0001c0005t0011g0006a0001c0005t0011g0371a0001c0005t0011g0372others(1): Show | 5 | HG00639.hp2 HG00735.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.1112-2908G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82775136 | ||||||
chr15:82775253
|
C | T | 20 | a0001c0001t0006g0016a0001c0001t0006g0017a0001c0001t0006g0019others(17): Show | 20 | HG00099.hp2 HG01106.hp1 HG01192.hp2 others(17): Show |
intron_variant | MODIFIER | c.1112-3025G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82775253 | ||||||
chr15:82775331
|
G | A | 1 | a0001c0001t0044g0164 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1112-3103C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82775331 | ||||||
chr15:82775397
|
C | CA | 47 | a0001c0001t0002g0087a0001c0001t0003g0201a0001c0001t0003g0206others(44): Show | 48 | HG00323.hp1 HG00408.hp2 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.1112-3170dupT | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82775397 | ||||||
chr15:82775419
|
A | G | 3 | a0001c0001t0013g0167a0001c0001t0013g0168a0001c0001t0043g0166 | 3 | HG02895.hp1 HG03139.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1112-3191T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82775419 | ||||||
chr15:82775938
|
T | G | 1 | a0001c0002t0001g0065 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1111+2828A>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82775938 | ||||||
chr15:82775968
|
A | G | 1 | a0001c0001t0006g0120 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1111+2798T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82775968 | ||||||
chr15:82776148
|
A | G | 4 | a0001c0005t0011g0006a0001c0005t0011g0371a0001c0005t0011g0372others(1): Show | 5 | HG00639.hp2 HG00735.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.1111+2618T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82776148 | ||||||
chr15:82776198
|
G | A | 4 | a0001c0001t0003g0183a0001c0001t0003g0279a0001c0001t0003g0302others(1): Show | 4 | HG02132.hp1 HG02135.hp2 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.1111+2568C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82776198 | ||||||
chr15:82776327
|
T | C | 4 | a0001c0002t0001g0055a0001c0002t0001g0060a0001c0002t0001g0061others(1): Show | 4 | HG01243.hp1 HG02257.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.1111+2439A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82776327 | ||||||
chr15:82776331
|
A | C | 6 | a0001c0001t0006g0031a0001c0001t0006g0119a0001c0001t0006g0120others(3): Show | 6 | HG01346.hp2 HG02630.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1111+2435T>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82776331 | ||||||
chr15:82776365
|
C | T | 4 | a0001c0005t0011g0006a0001c0005t0011g0371a0001c0005t0011g0372others(1): Show | 5 | HG00639.hp2 HG00735.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.1111+2401G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82776365 | ||||||
chr15:82776586
|
C | T | 131 | a0001c0001t0002g0087a0001c0001t0006g0016a0001c0001t0006g0017others(128): Show | 132 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.1111+2180G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82776586 | ||||||
chr15:82776631
|
GA | G | 11 | a0001c0001t0002g0127a0001c0001t0002g0128a0001c0001t0002g0139others(8): Show | 11 | HG02602.hp2 HG02698.hp2 HG03017.hp1 others(8): Show |
intron_variant | MODIFIER | c.1111+2134delT | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82776631 | ||||||
chr15:82776674
|
C | A | 1 | a0005c0007t0033g0029 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1111+2092G>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82776674 | ||||||
chr15:82777113
|
A | G | 3 | a0002c0003t0012g0331a0002c0003t0012g0338a0002c0003t0039g0325 | 3 | NA18953.hp2 NA19010.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.1111+1653T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82777113 | ||||||
chr15:82777276
|
A | C | 3 | a0001c0001t0030g0288a0001c0001t0030g0289a0001c0001t0044g0164 | 3 | HG03486.hp2 HG03579.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1111+1490T>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82777276 | ||||||
chr15:82777555
|
G | C | 9 | a0001c0001t0013g0167a0001c0001t0013g0168a0001c0001t0013g0176others(6): Show | 9 | HG02895.hp1 HG02965.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.1111+1211C>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82777555 | ||||||
chr15:82777850
|
T | TA | 22 | a0001c0001t0003g0140a0001c0001t0003g0141a0001c0001t0006g0016others(19): Show | 22 | HG00099.hp2 HG01069.hp2 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.1111+915dupT | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82777850 | ||||||
chr15:82777936
|
T | C | 1 | a0001c0001t0035g0231 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1111+830A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82777936 | ||||||
chr15:82777973
|
C | T | 56 | a0002c0003t0004g0004a0002c0003t0004g0083a0002c0003t0004g0111others(53): Show | 57 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.1111+793G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82777973 | ||||||
chr15:82778011
|
C | G | 1 | a0001c0001t0008g0269 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1111+755G>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82778011 | ||||||
chr15:82778127
|
C | CAT | 27 | a0001c0001t0002g0128a0001c0001t0002g0139a0001c0001t0002g0149others(24): Show | 27 | HG00423.hp1 HG00558.hp1 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.1111+637_1111+638d others(4): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82778127 | ||||||
chr15:82778127
|
C | CATAT | 23 | a0001c0001t0002g0127a0001c0001t0002g0294a0001c0001t0002g0316others(20): Show | 25 | HG00323.hp1 HG01069.hp1 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.1111+635_1111+638d others(6): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82778127 | ||||||
chr15:82778127
|
C | CATATAT | 39 | a0001c0001t0003g0015a0001c0001t0003g0170a0001c0001t0003g0172others(36): Show | 39 | HG00140.hp1 HG00609.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.1111+633_1111+638d others(8): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82778127 | ||||||
chr15:82778127
|
C | CATATATA others(1): Show |
48 | a0001c0001t0002g0084a0001c0001t0002g0085a0001c0001t0003g0014others(45): Show | 48 | HG00140.hp2 HG00408.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.1111+631_1111+638d others(10): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82778127 | ||||||
chr15:82778127
|
C | CATATATA others(3): Show |
23 | a0001c0001t0003g0088a0001c0001t0003g0181a0001c0001t0003g0184others(20): Show | 23 | HG00544.hp2 HG00738.hp2 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.1111+629_1111+638d others(12): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82778127 | ||||||
chr15:82778127
|
C | CATATATA others(5): Show |
21 | a0001c0001t0003g0177a0001c0001t0003g0188a0001c0001t0003g0208others(18): Show | 21 | HG00597.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.1111+627_1111+638d others(14): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82778127 | ||||||
chr15:82778127
|
C | CATATATA others(7): Show |
14 | a0001c0001t0002g0121a0001c0001t0003g0210a0001c0001t0010g0197others(11): Show | 17 | HG00609.hp2 HG01891.hp2 HG02273.hp1 others(14): Show |
intron_variant | MODIFIER | c.1111+625_1111+638d others(16): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82778127 | ||||||
chr15:82778127
|
C | CATATATA others(9): Show |
13 | a0001c0001t0003g0262a0001c0001t0013g0178a0001c0001t0013g0324others(10): Show | 13 | HG00323.hp2 HG01074.hp1 HG01517.hp2 others(10): Show |
intron_variant | MODIFIER | c.1111+623_1111+638d others(18): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82778127 | ||||||
chr15:82778127
|
C | CATATATA others(11): Show |
4 | a0001c0001t0013g0168a0001c0001t0026g0248a0001c0002t0001g0061others(1): Show | 4 | HG02895.hp2 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1111+621_1111+638d others(20): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82778127 | ||||||
chr15:82778127
|
C | CATATATA others(13): Show |
5 | a0001c0001t0002g0304a0001c0001t0015g0219a0001c0001t0015g0220others(2): Show | 5 | HG01515.hp2 HG02257.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1111+619_1111+638d others(22): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82778127 | ||||||
chr15:82778127
|
C | CATATATA others(15): Show |
5 | a0001c0001t0002g0274a0001c0001t0024g0374a0001c0001t0024g0375others(2): Show | 5 | HG01070.hp1 HG01071.hp2 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.1111+617_1111+638d others(24): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82778127 | ||||||
chr15:82778127
|
C | CATATATA others(17): Show |
6 | a0001c0001t0003g0329a0001c0001t0015g0221a0001c0001t0027g0272others(3): Show | 6 | HG01099.hp1 HG02896.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1111+615_1111+638d others(26): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82778127 | ||||||
chr15:82778127
|
C | CATATATA others(23): Show |
2 | a0001c0001t0002g0087a0003c0004t0032g0138 | 2 | HG02486.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.1111+609_1111+638d others(32): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82778127 | ||||||
chr15:82778127
|
CAT | C | 62 | a0001c0001t0002g0292a0001c0001t0002g0293a0001c0001t0002g0295others(59): Show | 63 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.1111+637_1111+638d others(4): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82778127 | ||||||
chr15:82778127
|
CATAT | C | 9 | a0001c0001t0006g0119a0001c0001t0006g0120a0001c0001t0006g0285others(6): Show | 9 | HG01346.hp2 HG01361.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1111+635_1111+638d others(6): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82778127 | ||||||
chr15:82778127
|
CATATAT | C | 8 | a0001c0001t0023g0009a0001c0002t0001g0097a0001c0005t0011g0006others(5): Show | 9 | HG00639.hp2 HG00735.hp1 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.1111+633_1111+638d others(8): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82778127 | ||||||
chr15:82778137
|
T | TATATATA others(8): Show |
1 | a0001c0001t0003g0330 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1111+614_1111+628d others(17): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82778137 | ||||||
chr15:82778157
|
T | TATAA | 3 | a0001c0001t0003g0169a0001c0001t0017g0235a0001c0001t0017g0263 | 3 | HG02818.hp2 HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1111+608_1111+609i others(6): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82778157 | ||||||
chr15:82778157
|
T | TATATATA others(3): Show |
1 | a0001c0001t0003g0257 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1111+608_1111+609i others(12): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82778157 | ||||||
chr15:82778158
|
A | ATATATAT others(10): Show |
1 | a0001c0001t0008g0239 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1111+607_1111+608i others(19): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82778158 | ||||||
chr15:82778158
|
A | ATATATAT others(14): Show |
1 | a0001c0001t0008g0269 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1111+607_1111+608i others(23): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82778158 | ||||||
chr15:82778158
|
A | ATATATAT others(18): Show |
1 | a0001c0001t0008g0271 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1111+607_1111+608i others(27): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82778158 | ||||||
chr15:82778158
|
A | ATATATAT others(20): Show |
3 | a0001c0001t0008g0143a0001c0001t0008g0214a0001c0001t0008g0270 | 3 | HG02451.hp2 HG02486.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1111+607_1111+608i others(29): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82778158 | ||||||
chr15:82778158
|
A | ATATATAT others(22): Show |
1 | a0001c0001t0008g0215 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1111+607_1111+608i others(31): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82778158 | ||||||
chr15:82778467
|
T | TA | 3 | a0001c0002t0001g0058a0001c0002t0001g0092a0001c0002t0016g0091 | 3 | HG02135.hp1 HG02523.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.1111+298dupT | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82778467 | ||||||
chr15:82778479
|
A | G | 1 | a0001c0001t0003g0258 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1111+287T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82778479 | ||||||
chr15:82778740
|
C | T | 3 | a0001c0001t0024g0374a0001c0001t0024g0375a0001c0001t0024g0376 | 3 | HG01070.hp1 HG01071.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.1111+26G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82778740 | ||||||
chr15:82778742
|
C | T | 1 | a0001c0001t0029g0207 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1111+24G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82778742 | ||||||
chr15:82778919
|
T | C | 3 | a0001c0001t0023g0009a0001c0008t0023g0286a0001c0008t0023g0287 | 3 | HG01884.hp2 HG01891.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.990-32A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 5/12 | chr15 | 82778919 | ||||||
chr15:82779036
|
C | G | 56 | a0002c0003t0004g0004a0002c0003t0004g0083a0002c0003t0004g0111others(53): Show | 57 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.990-149G>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 5/12 | chr15 | 82779036 | ||||||
chr15:82779337
|
G | A | 2 | a0001c0001t0017g0236a0001c0001t0017g0263 | 2 | HG03098.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.990-450C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 5/12 | chr15 | 82779337 | ||||||
chr15:82779605
|
G | A | 1 | a0001c0001t0002g0216 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.989+640C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 5/12 | chr15 | 82779605 | ||||||
chr15:82779653
|
C | T | 1 | a0001c0001t0002g0047 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.989+592G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 5/12 | chr15 | 82779653 | ||||||
chr15:82779664
|
C | CA | 25 | a0001c0001t0013g0167a0001c0001t0013g0168a0001c0001t0013g0176others(22): Show | 25 | HG01109.hp1 HG01243.hp1 HG02071.hp1 others(22): Show |
intron_variant | MODIFIER | c.989+580dupT | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 5/12 | chr15 | 82779664 | ||||||
chr15:82779664
|
CA | C | 9 | a0001c0001t0003g0177a0001c0001t0003g0209a0001c0001t0003g0232others(6): Show | 9 | HG00597.hp2 HG01074.hp1 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.989+580delT | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 5/12 | chr15 | 82779664 | ||||||
chr15:82779679
|
A | G | 1 | a0001c0001t0006g0027 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.989+566T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 5/12 | chr15 | 82779679 | ||||||
chr15:82779718
|
C | A | 4 | a0001c0005t0011g0006a0001c0005t0011g0371a0001c0005t0011g0372others(1): Show | 5 | HG00639.hp2 HG00735.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.989+527G>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 5/12 | chr15 | 82779718 | ||||||
chr15:82779738
|
C | T | 188 | a0001c0001t0002g0087a0001c0001t0006g0016a0001c0001t0006g0017others(185): Show | 191 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.989+507G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 5/12 | chr15 | 82779738 | ||||||
chr15:82779932
|
T | C | 316 | a0001c0001t0002g0036a0001c0001t0002g0038a0001c0001t0002g0039others(313): Show | 323 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.989+313A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 5/12 | chr15 | 82779932 | ||||||
chr15:82780226
|
A | G | 1 | a0001c0001t0042g0033 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.989+19T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 5/12 | chr15 | 82780226 | ||||||
chr15:82780278
|
A | G | 5 | a0002c0003t0004g0336a0002c0003t0004g0347a0002c0003t0004g0350others(2): Show | 5 | HG02083.hp1 NA18975.hp1 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.967-11T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82780278 | ||||||
chr15:82780337
|
CT | C | 6 | a0001c0001t0025g0251a0001c0002t0001g0060a0001c0005t0011g0006others(3): Show | 7 | HG00639.hp2 HG00735.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.967-71delA | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82780337 | ||||||
chr15:82780371
|
GT | G | 4 | a0001c0005t0011g0006a0001c0005t0011g0371a0001c0005t0011g0372others(1): Show | 5 | HG00639.hp2 HG00735.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.967-105delA | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82780371 | ||||||
chr15:82780448
|
C | T | 6 | a0001c0001t0015g0219a0001c0001t0015g0220a0001c0001t0015g0221others(3): Show | 6 | HG02257.hp1 HG02572.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.967-181G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82780448 | ||||||
chr15:82780518
|
A | T | 6 | a0001c0001t0003g0169a0001c0001t0003g0257a0001c0001t0003g0258others(3): Show | 6 | HG02451.hp1 HG02818.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.967-251T>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82780518 | ||||||
chr15:82780527
|
G | A | 4 | a0001c0001t0023g0009a0001c0005t0011g0371a0001c0008t0023g0286others(1): Show | 4 | HG01361.hp2 HG01884.hp2 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.967-260C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82780527 | ||||||
chr15:82780585
|
G | A | 2 | a0002c0003t0004g0335a0002c0003t0004g0339 | 2 | HG02015.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.967-318C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82780585 | ||||||
chr15:82780627
|
C | G | 6 | a0001c0001t0013g0167a0001c0001t0013g0168a0001c0001t0013g0176others(3): Show | 6 | HG02895.hp1 HG02965.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.967-360G>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82780627 | ||||||
chr15:82780704
|
A | G | 1 | a0001c0002t0001g0284 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.967-437T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82780704 | ||||||
chr15:82780867
|
T | C | 1 | a0001c0001t0003g0262 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.967-600A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82780867 | ||||||
chr15:82780891
|
C | T | 1 | a0001c0001t0051g0315 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.967-624G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82780891 | ||||||
chr15:82781161
|
G | A | 3 | a0001c0002t0001g0058a0001c0002t0001g0092a0001c0002t0016g0091 | 3 | HG02135.hp1 HG02523.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.967-894C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82781161 | ||||||
chr15:82781161
|
G | T | 2 | a0001c0001t0013g0178a0001c0001t0013g0324 | 2 | HG02965.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.967-894C>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82781161 | ||||||
chr15:82781311
|
G | A | 1 | a0001c0001t0013g0176 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.967-1044C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82781311 | ||||||
chr15:82781349
|
C | T | 1 | a0001c0002t0001g0058 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.967-1082G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82781349 | ||||||
chr15:82781613
|
AATTAGGA others(10): Show |
A | 1 | a0001c0001t0010g0185 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.966+1165_966+1181d others(19): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82781613 | ||||||
chr15:82781638
|
T | C | 6 | a0001c0001t0023g0009a0001c0001t0042g0033a0001c0008t0023g0286others(3): Show | 6 | HG01884.hp2 HG01891.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.966+1157A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82781638 | ||||||
chr15:82781649
|
G | A | 6 | a0001c0001t0023g0009a0001c0001t0042g0033a0001c0008t0023g0286others(3): Show | 6 | HG01884.hp2 HG01891.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.966+1146C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82781649 | ||||||
chr15:82781674
|
A | G | 6 | a0001c0002t0001g0054a0001c0002t0001g0095a0001c0002t0001g0097others(3): Show | 6 | HG02074.hp2 NA18967.hp2 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.966+1121T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82781674 | ||||||
chr15:82781710
|
T | C | 1 | a0001c0001t0042g0033 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.966+1085A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82781710 | ||||||
chr15:82781773
|
C | G | 1 | a0001c0001t0042g0033 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.966+1022G>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82781773 | ||||||
chr15:82781787
|
C | T | 2 | a0001c0001t0025g0229a0001c0001t0025g0251 | 2 | NA18982.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.966+1008G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82781787 | ||||||
chr15:82781941
|
G | T | 3 | a0001c0001t0006g0031a0001c0001t0006g0119a0001c0001t0006g0120 | 3 | HG01346.hp2 HG02886.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.966+854C>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82781941 | ||||||
chr15:82781969
|
C | T | 3 | a0001c0002t0001g0067a0001c0002t0001g0068a0001c0002t0001g0156 | 3 | HG00323.hp1 HG01346.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.966+826G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82781969 | ||||||
chr15:82781989
|
G | A | 2 | a0001c0001t0013g0178a0001c0001t0013g0324 | 2 | HG02965.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.966+806C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82781989 | ||||||
chr15:82782065
|
A | AAAT | 26 | a0001c0001t0002g0047a0001c0001t0002g0275a0001c0001t0002g0308others(23): Show | 26 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(23): Show |
intron_variant | MODIFIER | c.966+727_966+729dup others(3): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82782065 | ||||||
chr15:82782065
|
A | AAATAAT | 51 | a0001c0001t0002g0294a0001c0001t0002g0307a0001c0001t0006g0027others(48): Show | 55 | HG00423.hp2 HG00544.hp1 HG01928.hp1 others(52): Show |
intron_variant | MODIFIER | c.966+724_966+729dup others(6): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82782065 | ||||||
chr15:82782065
|
A | AAATAATA others(2): Show |
39 | a0001c0001t0002g0085a0001c0001t0002g0292a0001c0001t0002g0293others(36): Show | 41 | HG00733.hp1 HG00733.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.966+721_966+729dup others(9): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82782065 | ||||||
chr15:82782065
|
A | AAATAATA others(5): Show |
18 | a0001c0001t0002g0084a0001c0001t0002g0295a0001c0001t0021g0291others(15): Show | 18 | HG00323.hp2 HG00639.hp2 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.966+718_966+729dup others(12): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82782065 | ||||||
chr15:82782065
|
AAAT | A | 8 | a0001c0001t0003g0233a0001c0001t0003g0257a0001c0001t0003g0259others(5): Show | 8 | HG00673.hp2 HG01361.hp1 HG01516.hp1 others(5): Show |
intron_variant | MODIFIER | c.966+727_966+729del others(3): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82782065 | ||||||
chr15:82782065
|
AAATAAT | A | 87 | a0001c0001t0002g0121a0001c0001t0002g0174a0001c0001t0002g0175others(84): Show | 87 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.966+724_966+729del others(6): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82782065 | ||||||
chr15:82782104
|
T | A | 9 | a0001c0001t0002g0237a0001c0001t0013g0167a0001c0001t0013g0168others(6): Show | 9 | HG01109.hp1 HG02886.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.966+691A>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82782104 | ||||||
chr15:82782104
|
T | TAATAAA | 19 | a0001c0001t0002g0036a0001c0001t0002g0038a0001c0001t0002g0039others(16): Show | 19 | HG00673.hp1 HG01346.hp1 HG02074.hp2 others(16): Show |
intron_variant | MODIFIER | c.966+690_966+691ins others(6): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82782104 | ||||||
chr15:82782104
|
T | TAATAATA others(2): Show |
28 | a0001c0001t0002g0041a0001c0001t0002g0087a0001c0001t0044g0164others(25): Show | 29 | HG00408.hp2 HG00639.hp1 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.966+690_966+691ins others(9): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82782104 | ||||||
chr15:82782104
|
T | TAATAATA others(5): Show |
1 | a0001c0001t0030g0288 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.966+690_966+691ins others(12): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82782104 | ||||||
chr15:82782104
|
T | TAATAATA others(5): Show |
33 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0030others(30): Show | 33 | HG00323.hp1 HG00609.hp1 HG01516.hp2 others(30): Show |
intron_variant | MODIFIER | c.966+690_966+691ins others(12): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82782104 | ||||||
chr15:82782104
|
T | TAATAATA others(6): Show |
4 | a0001c0002t0001g0055a0001c0002t0001g0060a0001c0002t0001g0061others(1): Show | 4 | HG01243.hp1 HG02257.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.966+690_966+691ins others(13): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82782104 | ||||||
chr15:82782104
|
T | TAATAATA others(8): Show |
1 | a0001c0001t0030g0289 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.966+690_966+691ins others(15): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82782104 | ||||||
chr15:82782104
|
T | TAATAATA others(8): Show |
12 | a0001c0001t0059g0124a0001c0002t0001g0037a0001c0002t0001g0056others(9): Show | 12 | HG01943.hp1 HG02280.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.966+690_966+691ins others(15): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82782104 | ||||||
chr15:82782111
|
C | A | 3 | a0001c0002t0001g0241a0001c0002t0001g0327a0001c0002t0022g0225 | 3 | HG01109.hp1 HG02922.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.966+684G>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82782111 | ||||||
chr15:82782171
|
G | A | 9 | a0001c0001t0002g0036a0001c0001t0002g0038a0001c0001t0002g0039others(6): Show | 9 | NA18964.hp1 NA18972.hp2 NA18981.hp1 others(6): Show |
intron_variant | MODIFIER | c.966+624C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82782171 | ||||||
chr15:82782192
|
A | G | 6 | a0001c0001t0013g0167a0001c0001t0013g0168a0001c0001t0013g0176others(3): Show | 6 | HG02895.hp1 HG02965.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.966+603T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82782192 | ||||||
chr15:82782204
|
G | A | 1 | a0001c0002t0053g0046 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.966+591C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82782204 | ||||||
chr15:82782205
|
C | G | 93 | a0001c0001t0003g0014a0001c0001t0003g0015a0001c0001t0003g0026others(90): Show | 93 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.966+590G>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82782205 | ||||||
chr15:82782269
|
G | A | 1 | a0001c0001t0002g0148 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.966+526C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82782269 | ||||||
chr15:82782285
|
A | G | 1 | a0002c0003t0004g0364 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.966+510T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82782285 | ||||||
chr15:82782300
|
T | C | 1 | a0001c0001t0003g0354 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.966+495A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82782300 | ||||||
chr15:82782325
|
A | G | 1 | a0001c0001t0002g0038 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.966+470T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82782325 | ||||||
chr15:82782395
|
G | A | 2 | a0001c0001t0002g0121a0001c0001t0002g0274 | 2 | HG01891.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.966+400C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82782395 | ||||||
chr15:82782417
|
A | C | 111 | a0001c0001t0002g0036a0001c0001t0002g0038a0001c0001t0002g0039others(108): Show | 113 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.966+378T>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82782417 | ||||||
chr15:82782436
|
A | G | 2 | a0003c0004t0005g0132a0003c0004t0005g0133 | 2 | HG01258.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.966+359T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82782436 | ||||||
chr15:82782574
|
C | T | 1 | a0001c0002t0034g0034 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.966+221G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82782574 | ||||||
chr15:82782609
|
T | C | 164 | a0001c0001t0002g0174a0001c0001t0002g0175a0001c0001t0002g0216others(161): Show | 165 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.966+186A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82782609 | ||||||
chr15:82782615
|
C | T | 1 | a0001c0001t0002g0275 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.966+180G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82782615 | ||||||
chr15:82782645
|
A | G | 1 | a0001c0001t0003g0210 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.966+150T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82782645 | ||||||
chr15:82782731
|
G | A | 3 | a0002c0003t0004g0350a0002c0003t0004g0351a0010c0010t0004g0358 | 3 | NA18975.hp1 NA19065.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.966+64C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82782731 | ||||||
chr15:82782763
|
T | A | 1 | a0001c0001t0008g0239 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.966+32A>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82782763 | ||||||
chr15:82783297
|
T | C | 325 | a0001c0001t0002g0036a0001c0001t0002g0038a0001c0001t0002g0039others(322): Show | 332 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(329): Show |
intron_variant | MODIFIER | c.736-272A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82783297 | ||||||
chr15:82783342
|
G | A | 4 | a0001c0005t0011g0006a0001c0005t0011g0371a0001c0005t0011g0372others(1): Show | 5 | HG00639.hp2 HG00735.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.736-317C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82783342 | ||||||
chr15:82783478
|
G | C | 1 | a0001c0001t0003g0169 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.736-453C>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82783478 | ||||||
chr15:82783676
|
A | C | 56 | a0002c0003t0004g0004a0002c0003t0004g0083a0002c0003t0004g0111others(53): Show | 57 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.736-651T>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82783676 | ||||||
chr15:82783681
|
G | C | 1 | a0001c0001t0059g0124 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.736-656C>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82783681 | ||||||
chr15:82783759
|
C | T | 1 | a0001c0001t0003g0354 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.736-734G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82783759 | ||||||
chr15:82783859
|
G | A | 1 | a0001c0001t0003g0330 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.736-834C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82783859 | ||||||
chr15:82783859
|
G | T | 3 | a0001c0002t0001g0098a0001c0002t0001g0109a0001c0002t0001g0162 | 3 | HG02074.hp2 NA19062.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.736-834C>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82783859 | ||||||
chr15:82783870
|
C | T | 1 | a0001c0001t0003g0190 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.736-845G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82783870 | ||||||
chr15:82784056
|
A | G | 1 | a0001c0001t0002g0087 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.736-1031T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82784056 | ||||||
chr15:82784114
|
T | A | 1 | a0010c0010t0004g0358 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.736-1089A>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82784114 | ||||||
chr15:82784121
|
G | T | 1 | a0010c0010t0004g0358 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.736-1096C>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82784121 | ||||||
chr15:82784124
|
A | T | 1 | a0010c0010t0004g0358 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.736-1099T>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82784124 | ||||||
chr15:82784129
|
G | T | 1 | a0010c0010t0004g0358 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.736-1104C>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82784129 | ||||||
chr15:82784133
|
A | T | 1 | a0010c0010t0004g0358 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.736-1108T>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82784133 | ||||||
chr15:82784142
|
C | G | 1 | a0010c0010t0004g0358 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.736-1117G>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82784142 | ||||||
chr15:82784143
|
T | A | 1 | a0010c0010t0004g0358 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.736-1118A>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82784143 | ||||||
chr15:82784177
|
G | T | 1 | a0010c0010t0004g0358 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.736-1152C>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82784177 | ||||||
chr15:82784182
|
A | T | 1 | a0010c0010t0004g0358 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.736-1157T>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82784182 | ||||||
chr15:82784183
|
A | T | 1 | a0010c0010t0004g0358 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.736-1158T>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82784183 | ||||||
chr15:82784185
|
G | A | 1 | a0010c0010t0004g0358 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.736-1160C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82784185 | ||||||
chr15:82784194
|
T | G | 1 | a0010c0010t0004g0358 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.736-1169A>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82784194 | ||||||
chr15:82784206
|
C | G | 1 | a0010c0010t0004g0358 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.736-1181G>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82784206 | ||||||
chr15:82784207
|
T | C | 1 | a0010c0010t0004g0358 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.736-1182A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82784207 | ||||||
chr15:82784208
|
G | A | 1 | a0010c0010t0004g0358 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.736-1183C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82784208 | ||||||
chr15:82784230
|
T | TTTTTA | 125 | a0001c0001t0002g0087a0001c0001t0003g0014a0001c0001t0003g0015others(122): Show | 126 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.736-1210_736-1206d others(7): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82784230 | ||||||
chr15:82784230
|
T | TTTTTATT others(3): Show |
3 | a0001c0002t0001g0067a0001c0002t0001g0068a0001c0002t0022g0093 | 3 | HG01346.hp1 HG01952.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.736-1215_736-1206d others(12): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82784230 | ||||||
chr15:82784250
|
AT | A | 14 | a0002c0003t0004g0004a0002c0003t0004g0083a0002c0003t0004g0147others(11): Show | 15 | HG00423.hp2 HG00735.hp2 HG01928.hp1 others(12): Show |
intron_variant | MODIFIER | c.736-1226delA | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82784250 | ||||||
chr15:82784252
|
T | G | 1 | a0001c0002t0001g0073 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.736-1227A>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82784252 | ||||||
chr15:82784254
|
T | A | 47 | a0001c0001t0013g0167a0001c0001t0013g0168a0001c0001t0013g0178others(44): Show | 47 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.736-1229A>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82784254 | ||||||
chr15:82784255
|
A | T | 50 | a0001c0001t0002g0047a0001c0001t0013g0167a0001c0001t0013g0168others(47): Show | 53 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.736-1230T>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82784255 | ||||||
chr15:82784260
|
T | A | 129 | a0001c0001t0002g0036a0001c0001t0002g0038a0001c0001t0002g0039others(126): Show | 130 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.736-1235A>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82784260 | ||||||
chr15:82784290
|
G | A | 1 | a0001c0001t0006g0024 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.736-1265C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82784290 | ||||||
chr15:82784492
|
C | A | 2 | a0003c0004t0005g0180a0003c0004t0032g0138 | 2 | HG01099.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.736-1467G>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82784492 | ||||||
chr15:82784527
|
G | A | 1 | a0001c0002t0060g0110 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.736-1502C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82784527 | ||||||
chr15:82784586
|
C | G | 4 | a0001c0005t0011g0006a0001c0005t0011g0371a0001c0005t0011g0372others(1): Show | 5 | HG00639.hp2 HG00735.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.736-1561G>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82784586 | ||||||
chr15:82784743
|
A | G | 332 | a0001c0001t0002g0036a0001c0001t0002g0038a0001c0001t0002g0039others(329): Show | 339 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(336): Show |
intron_variant | MODIFIER | c.736-1718T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82784743 | ||||||
chr15:82784844
|
G | T | 1 | a0001c0001t0003g0189 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.735+1667C>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82784844 | ||||||
chr15:82784852
|
C | G | 1 | a0001c0001t0003g0354 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.735+1659G>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82784852 | ||||||
chr15:82785300
|
A | ATTAT | 112 | a0001c0001t0002g0036a0001c0001t0002g0038a0001c0001t0002g0112others(109): Show | 113 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.735+1207_735+1210d others(6): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82785300 | ||||||
chr15:82785300
|
A | ATTATTTA others(1): Show |
25 | a0001c0001t0002g0087a0001c0001t0003g0210a0001c0001t0008g0214others(22): Show | 25 | HG00609.hp2 HG01943.hp1 HG02040.hp2 others(22): Show |
intron_variant | MODIFIER | c.735+1203_735+1210d others(10): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82785300 | ||||||
chr15:82785300
|
ATTAT | A | 13 | a0001c0001t0003g0169a0001c0001t0003g0233a0001c0001t0003g0258others(10): Show | 16 | HG02257.hp1 HG02451.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.735+1207_735+1210d others(6): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82785300 | ||||||
chr15:82785300
|
ATTATTTA others(5): Show |
A | 8 | a0001c0001t0003g0206a0001c0001t0003g0234a0001c0001t0003g0253others(5): Show | 8 | HG03471.hp1 HG03486.hp2 HG03579.hp1 others(5): Show |
intron_variant | MODIFIER | c.735+1199_735+1210d others(14): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82785300 | ||||||
chr15:82785323
|
AT | A | 19 | a0001c0001t0013g0282a0003c0004t0005g0003a0003c0004t0005g0010others(16): Show | 20 | HG00323.hp2 HG00738.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.735+1187delA | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82785323 | ||||||
chr15:82785355
|
C | T | 2 | a0001c0001t0002g0121a0001c0001t0002g0274 | 2 | HG01891.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.735+1156G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82785355 | ||||||
chr15:82785436
|
T | A | 2 | a0001c0001t0009g0011a0001c0001t0009g0050 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.735+1075A>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82785436 | ||||||
chr15:82785530
|
G | A | 56 | a0002c0003t0004g0004a0002c0003t0004g0083a0002c0003t0004g0111others(53): Show | 57 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.735+981C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82785530 | ||||||
chr15:82785601
|
G | A | 1 | a0002c0003t0018g0357 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.735+910C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82785601 | ||||||
chr15:82785613
|
C | T | 5 | a0001c0001t0030g0288a0001c0001t0030g0289a0001c0001t0044g0164others(2): Show | 5 | HG03471.hp1 HG03486.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.735+898G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82785613 | ||||||
chr15:82785700
|
A | G | 1 | a0001c0001t0003g0188 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.735+811T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82785700 | ||||||
chr15:82785772
|
A | AC | 8 | a0001c0001t0002g0174a0001c0001t0003g0250a0001c0001t0010g0196others(5): Show | 8 | HG00438.hp1 HG01109.hp2 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.735+738dupG | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82785772 | ||||||
chr15:82785871
|
G | A | 3 | a0001c0001t0026g0246a0001c0001t0026g0248a0001c0002t0001g0247 | 3 | HG01109.hp2 HG02280.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.735+640C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82785871 | ||||||
chr15:82786385
|
A | G | 189 | a0001c0001t0002g0036a0001c0001t0002g0038a0001c0001t0002g0039others(186): Show | 195 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.735+126T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82786385 | ||||||
chr15:82786671
|
G | A | 19 | a0001c0001t0013g0282a0003c0004t0005g0003a0003c0004t0005g0126others(16): Show | 20 | HG00323.hp2 HG00738.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.640-65C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 2/12 | chr15 | 82786671 | ||||||
chr15:82786716
|
T | C | 1 | a0001c0001t0008g0271 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.639+36A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 2/12 | chr15 | 82786716 | ||||||
chr15:82787614
|
A | AT | 8 | a0001c0001t0002g0174a0001c0001t0002g0175a0001c0001t0002g0216others(5): Show | 8 | HG02109.hp1 HG02622.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.-78-147dupA | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82787614 | ||||||
chr15:82787618
|
G | T | 8 | a0001c0001t0002g0174a0001c0001t0002g0175a0001c0001t0002g0216others(5): Show | 8 | HG02109.hp1 HG02622.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.-78-150C>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82787618 | ||||||
chr15:82787663
|
G | T | 1 | a0002c0003t0018g0346 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-78-195C>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82787663 | ||||||
chr15:82787720
|
TA | T | 64 | a0001c0001t0013g0167a0001c0001t0013g0168a0001c0001t0013g0176others(61): Show | 65 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.-78-253delT | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82787720 | ||||||
chr15:82787723
|
A | G | 13 | a0001c0001t0008g0143a0001c0001t0008g0214a0001c0001t0008g0239others(10): Show | 13 | HG01109.hp1 HG02055.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.-78-255T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82787723 | ||||||
chr15:82788056
|
G | A | 1 | a0001c0002t0001g0094 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-78-588C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82788056 | ||||||
chr15:82788221
|
C | T | 1 | a0001c0001t0002g0150 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-78-753G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82788221 | ||||||
chr15:82788300
|
G | A | 92 | a0001c0001t0002g0036a0001c0001t0002g0038a0001c0001t0002g0039others(89): Show | 93 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.-78-832C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82788300 | ||||||
chr15:82788326
|
T | C | 2 | a0001c0002t0001g0054a0001c0002t0001g0095 | 2 | NA18967.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.-78-858A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82788326 | ||||||
chr15:82788341
|
C | CA | 149 | a0001c0001t0002g0036a0001c0001t0002g0038a0001c0001t0002g0039others(146): Show | 151 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.-78-874dupT | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82788341 | ||||||
chr15:82788341
|
C | CAA | 11 | a0001c0001t0055g0122a0001c0002t0001g0057a0001c0002t0001g0058others(8): Show | 11 | HG01517.hp2 HG02074.hp2 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.-78-875_-78-874dup others(2): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82788341 | ||||||
chr15:82788341
|
CA | C | 58 | a0001c0001t0008g0143a0001c0001t0013g0176a0001c0001t0042g0033others(55): Show | 59 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.-78-874delT | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82788341 | ||||||
chr15:82788491
|
C | A | 4 | a0001c0005t0011g0006a0001c0005t0011g0371a0001c0005t0011g0372others(1): Show | 5 | HG00639.hp2 HG00735.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.-78-1023G>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82788491 | ||||||
chr15:82788494
|
G | A | 1 | a0001c0002t0001g0156 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-78-1026C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82788494 | ||||||
chr15:82788504
|
C | CA | 8 | a0001c0001t0002g0139a0001c0001t0002g0148a0001c0001t0002g0150others(5): Show | 8 | HG00099.hp1 HG00423.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.-78-1037dupT | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82788504 | ||||||
chr15:82788504
|
CA | C | 279 | a0001c0001t0002g0036a0001c0001t0002g0038a0001c0001t0002g0039others(276): Show | 285 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(282): Show |
intron_variant | MODIFIER | c.-78-1037delT | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82788504 | ||||||
chr15:82788504
|
CAA | C | 13 | a0001c0001t0003g0140a0001c0001t0006g0031a0001c0001t0010g0187others(10): Show | 13 | HG00323.hp2 HG01069.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.-78-1038_-78-1037d others(4): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82788504 | ||||||
chr15:82788577
|
A | T | 5 | a0001c0002t0001g0037a0001c0002t0007g0035a0001c0002t0007g0044others(2): Show | 5 | NA18956.hp1 NA18957.hp2 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.-78-1109T>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82788577 | ||||||
chr15:82788672
|
C | T | 190 | a0001c0001t0002g0036a0001c0001t0002g0038a0001c0001t0002g0039others(187): Show | 193 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.-78-1204G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82788672 | ||||||
chr15:82788977
|
TA | T | 63 | a0001c0001t0013g0167a0001c0001t0013g0168a0001c0001t0013g0176others(60): Show | 64 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.-78-1510delT | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82788977 | ||||||
chr15:82789057
|
G | A | 4 | a0001c0001t0023g0009a0001c0008t0023g0286a0001c0008t0023g0287others(1): Show | 4 | HG01884.hp2 HG01891.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-78-1589C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82789057 | ||||||
chr15:82789354
|
T | TATA | 37 | a0001c0001t0002g0047a0001c0001t0002g0121a0001c0001t0002g0149others(34): Show | 38 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.-78-1889_-78-1887d others(5): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82789354 | ||||||
chr15:82789354
|
T | TATAATA | 39 | a0001c0001t0002g0036a0001c0001t0002g0038a0001c0001t0002g0039others(36): Show | 39 | HG00673.hp1 HG01070.hp1 HG01071.hp2 others(36): Show |
intron_variant | MODIFIER | c.-78-1892_-78-1887d others(8): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82789354 | ||||||
chr15:82789354
|
T | TATAATAA others(2): Show |
40 | a0001c0001t0002g0040a0001c0001t0013g0178a0001c0001t0013g0324others(37): Show | 41 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(38): Show |
intron_variant | MODIFIER | c.-78-1895_-78-1887d others(11): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82789354 | ||||||
chr15:82789354
|
T | TATAATAA others(5): Show |
13 | a0001c0001t0002g0087a0001c0002t0001g0051a0001c0002t0001g0058others(10): Show | 13 | HG02080.hp2 HG02135.hp1 HG02155.hp1 others(10): Show |
intron_variant | MODIFIER | c.-78-1898_-78-1887d others(14): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82789354 | ||||||
chr15:82789354
|
TATA | T | 3 | a0001c0001t0002g0275a0002c0003t0004g0366a0005c0007t0033g0048 | 3 | HG02080.hp1 NA19043.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.-78-1889_-78-1887d others(5): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82789354 | ||||||
chr15:82789406
|
A | T | 92 | a0001c0001t0002g0036a0001c0001t0002g0038a0001c0001t0002g0039others(89): Show | 93 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.-78-1938T>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82789406 | ||||||
chr15:82789459
|
T | TACATTAT others(22): Show |
1 | a0001c0001t0059g0124 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-78-2020_-78-1992d others(31): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82789459 | ||||||
chr15:82789605
|
T | A | 1 | a0009c0014t0004g0243 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-78-2137A>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82789605 | ||||||
chr15:82789613
|
A | G | 124 | a0001c0001t0002g0036a0001c0001t0002g0038a0001c0001t0002g0039others(121): Show | 125 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.-78-2145T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82789613 | ||||||
chr15:82789635
|
T | C | 1 | a0001c0001t0002g0041 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-78-2167A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82789635 | ||||||
chr15:82790125
|
A | G | 11 | a0001c0001t0002g0127a0001c0001t0002g0128a0001c0001t0002g0139others(8): Show | 11 | HG02602.hp2 HG02698.hp2 HG03017.hp1 others(8): Show |
intron_variant | MODIFIER | c.-78-2657T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82790125 | ||||||
chr15:82790188
|
C | T | 1 | a0001c0001t0031g0218 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-78-2720G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82790188 | ||||||
chr15:82790189
|
G | GACA | 21 | a0001c0001t0013g0282a0003c0004t0005g0003a0003c0004t0005g0126others(18): Show | 22 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.-78-2724_-78-2722d others(5): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82790189 | ||||||
chr15:82790189
|
GACA | G | 183 | a0001c0001t0002g0036a0001c0001t0002g0038a0001c0001t0002g0039others(180): Show | 186 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.-78-2724_-78-2722d others(5): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82790189 | ||||||
chr15:82790189
|
GACAACA | G | 7 | a0002c0003t0004g0337a0002c0003t0004g0340a0002c0003t0004g0342others(4): Show | 7 | HG00423.hp2 HG02040.hp2 NA18969.hp2 others(4): Show |
intron_variant | MODIFIER | c.-78-2727_-78-2722d others(8): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82790189 | ||||||
chr15:82790206
|
CAACA | C | 6 | a0001c0001t0015g0219a0001c0001t0015g0220a0001c0001t0015g0221others(3): Show | 6 | HG02257.hp1 HG02572.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-78-2742_-78-2739d others(6): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82790206 | ||||||
chr15:82790427
|
C | T | 1 | a0003c0004t0032g0138 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-78-2959G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82790427 | ||||||
chr15:82790439
|
C | G | 1 | a0003c0004t0005g0003 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-78-2971G>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82790439 | ||||||
chr15:82790544
|
T | TGTGTGTG others(6): Show |
1 | a0001c0001t0009g0028 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-78-3077_-78-3076i others(15): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82790544 | ||||||
chr15:82790544
|
T | TGTGTGTG others(8): Show |
1 | a0001c0002t0001g0012 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-78-3077_-78-3076i others(17): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82790544 | ||||||
chr15:82790544
|
T | TTG | 56 | a0001c0001t0002g0149a0001c0001t0003g0354a0001c0001t0010g0185others(53): Show | 60 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.-78-3078_-78-3077d others(4): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82790544 | ||||||
chr15:82790544
|
T | TTGTG | 23 | a0001c0001t0002g0036a0001c0001t0002g0038a0001c0001t0002g0039others(20): Show | 24 | HG00639.hp2 HG00673.hp1 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.-78-3080_-78-3077d others(6): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82790544 | ||||||
chr15:82790544
|
T | TTGTGTG | 11 | a0001c0001t0013g0178a0001c0001t0013g0324a0001c0001t0023g0009others(8): Show | 11 | HG01884.hp2 HG01891.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-78-3082_-78-3077d others(8): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82790544 | ||||||
chr15:82790544
|
T | TTGTGTGT others(3): Show |
6 | a0001c0002t0001g0002a0001c0002t0001g0057a0001c0002t0001g0089others(3): Show | 7 | HG01069.hp1 HG01071.hp1 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.-78-3086_-78-3077d others(12): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82790544 | ||||||
chr15:82790544
|
T | TTGTGTGT others(5): Show |
27 | a0001c0001t0002g0087a0001c0001t0006g0016a0001c0001t0006g0017others(24): Show | 27 | HG00099.hp2 HG01106.hp1 HG01192.hp2 others(24): Show |
intron_variant | MODIFIER | c.-78-3088_-78-3077d others(14): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82790544 | ||||||
chr15:82790544
|
T | TTGTGTGT others(7): Show |
54 | a0001c0001t0002g0112a0001c0001t0009g0011a0001c0001t0009g0050others(51): Show | 54 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.-78-3090_-78-3077d others(16): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82790544 | ||||||
chr15:82790544
|
T | TTGTGTGT others(9): Show |
6 | a0001c0002t0001g0030a0001c0002t0001g0051a0001c0002t0001g0056others(3): Show | 6 | HG01243.hp2 HG02083.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.-78-3092_-78-3077d others(18): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82790544 | ||||||
chr15:82790544
|
T | TTGTGTGT others(11): Show |
2 | a0004c0006t0001g0099a0004c0006t0001g0100 | 2 | HG02922.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-78-3094_-78-3077d others(20): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82790544 | ||||||
chr15:82790544
|
T | TTGTGTGT others(13): Show |
1 | a0001c0002t0001g0058 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-78-3096_-78-3077d others(22): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82790544 | ||||||
chr15:82790618
|
T | C | 184 | a0001c0001t0002g0036a0001c0001t0002g0038a0001c0001t0002g0039others(181): Show | 187 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.-78-3150A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82790618 | ||||||
chr15:82790629
|
C | G | 2 | a0001c0005t0011g0371a0001c0005t0011g0372 | 2 | HG00639.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.-78-3161G>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82790629 | ||||||
chr15:82790644
|
C | T | 1 | a0005c0007t0033g0029 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-78-3176G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82790644 | ||||||
chr15:82790661
|
C | T | 115 | a0001c0001t0002g0036a0001c0001t0002g0038a0001c0001t0002g0039others(112): Show | 119 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.-78-3193G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82790661 | ||||||
chr15:82790662
|
G | A | 1 | a0001c0002t0007g0277 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-78-3194C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82790662 | ||||||
chr15:82790714
|
T | C | 4 | a0001c0002t0001g0055a0001c0002t0001g0060a0001c0002t0001g0061others(1): Show | 4 | HG01243.hp1 HG02257.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.-78-3246A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82790714 | ||||||
chr15:82790721
|
G | A | 3 | a0001c0001t0013g0178a0001c0001t0013g0324a0005c0007t0033g0048 | 3 | HG02965.hp2 HG02976.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-78-3253C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82790721 | ||||||
chr15:82790742
|
A | AT | 146 | a0001c0001t0002g0087a0001c0001t0002g0112a0001c0001t0002g0121others(143): Show | 147 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.-78-3275dupA | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82790742 | ||||||
chr15:82790742
|
A | ATT | 95 | a0001c0001t0002g0036a0001c0001t0002g0038a0001c0001t0002g0039others(92): Show | 96 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(93): Show |
intron_variant | MODIFIER | c.-78-3276_-78-3275d others(4): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82790742 | ||||||
chr15:82790809
|
T | A | 2 | a0001c0001t0002g0087a0001c0002t0016g0086 | 2 | HG02735.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.-78-3341A>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82790809 | ||||||
chr15:82790927
|
G | T | 24 | a0001c0001t0003g0088a0001c0001t0003g0186a0001c0001t0003g0188others(21): Show | 24 | HG00609.hp2 HG02015.hp1 HG02056.hp1 others(21): Show |
intron_variant | MODIFIER | c.-78-3459C>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82790927 | ||||||
chr15:82791148
|
G | A | 1 | a0001c0001t0029g0207 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-78-3680C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82791148 | ||||||
chr15:82791155
|
T | A | 1 | a0001c0001t0029g0207 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-78-3687A>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82791155 | ||||||
chr15:82791155
|
T | C | 1 | a0001c0001t0003g0259 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-78-3687A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82791155 | ||||||
chr15:82791209
|
A | G | 1 | a0001c0001t0002g0292 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-78-3741T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82791209 | ||||||
chr15:82791241
|
G | A | 1 | a0001c0001t0003g0169 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-78-3773C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82791241 | ||||||
chr15:82791258
|
A | G | 4 | a0001c0001t0023g0009a0001c0008t0023g0286a0001c0008t0023g0287others(1): Show | 4 | HG01884.hp2 HG01891.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-78-3790T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82791258 | ||||||
chr15:82791288
|
G | C | 4 | a0001c0002t0001g0037a0001c0002t0007g0035a0001c0002t0007g0044others(1): Show | 4 | NA18956.hp1 NA18957.hp2 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.-78-3820C>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82791288 | ||||||
chr15:82791289
|
C | A | 4 | a0001c0002t0001g0037a0001c0002t0007g0035a0001c0002t0007g0044others(1): Show | 4 | NA18956.hp1 NA18957.hp2 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.-78-3821G>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82791289 | ||||||
chr15:82791378
|
A | T | 4 | a0001c0005t0011g0006a0001c0005t0011g0371a0001c0005t0011g0372others(1): Show | 5 | HG00639.hp2 HG00735.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.-78-3910T>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82791378 | ||||||
chr15:82791430
|
A | G | 331 | a0001c0001t0002g0036a0001c0001t0002g0038a0001c0001t0002g0039others(328): Show | 338 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(335): Show |
intron_variant | MODIFIER | c.-78-3962T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82791430 | ||||||
chr15:82791651
|
A | G | 1 | a0001c0008t0023g0286 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-78-4183T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82791651 | ||||||
chr15:82791663
|
C | T | 1 | a0003c0004t0046g0129 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-78-4195G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82791663 | ||||||
chr15:82791732
|
C | T | 1 | a0001c0001t0042g0033 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-78-4264G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82791732 | ||||||
chr15:82791929
|
G | T | 3 | a0002c0003t0012g0331a0002c0003t0012g0338a0002c0003t0039g0325 | 3 | NA18953.hp2 NA19010.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.-78-4461C>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82791929 | ||||||
chr15:82791945
|
C | T | 52 | a0001c0001t0003g0354a0001c0001t0013g0167a0001c0001t0013g0168others(49): Show | 53 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.-78-4477G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82791945 | ||||||
chr15:82792119
|
G | T | 4 | a0001c0002t0001g0055a0001c0002t0001g0060a0001c0002t0001g0061others(1): Show | 4 | HG01243.hp1 HG02257.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.-78-4651C>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82792119 | ||||||
chr15:82792288
|
G | A | 51 | a0001c0001t0003g0354a0001c0001t0013g0167a0001c0001t0013g0168others(48): Show | 52 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.-78-4820C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82792288 | ||||||
chr15:82792491
|
A | G | 4 | a0001c0001t0023g0009a0001c0008t0023g0286a0001c0008t0023g0287others(1): Show | 4 | HG01884.hp2 HG01891.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-78-5023T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82792491 | ||||||
chr15:82792509
|
C | G | 190 | a0001c0001t0002g0036a0001c0001t0002g0038a0001c0001t0002g0039others(187): Show | 193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.-78-5041G>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82792509 | ||||||
chr15:82792780
|
G | A | 1 | a0001c0001t0003g0169 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-78-5312C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82792780 | ||||||
chr15:82792991
|
A | G | 1 | a0001c0001t0002g0150 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-78-5523T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82792991 | ||||||
chr15:82793121
|
G | A | 24 | a0001c0001t0002g0121a0001c0001t0003g0014a0001c0001t0003g0015others(21): Show | 24 | HG00099.hp2 HG00140.hp2 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.-78-5653C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82793121 | ||||||
chr15:82793142
|
C | G | 4 | a0001c0005t0011g0006a0001c0005t0011g0371a0001c0005t0011g0372others(1): Show | 5 | HG00639.hp2 HG00735.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.-78-5674G>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82793142 | ||||||
chr15:82793164
|
C | T | 21 | a0001c0001t0002g0127a0001c0001t0002g0128a0001c0001t0002g0139others(18): Show | 22 | HG00323.hp2 HG00738.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.-78-5696G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82793164 | ||||||
chr15:82793325
|
G | GT | 7 | a0001c0001t0002g0127a0001c0001t0002g0128a0001c0001t0002g0139others(4): Show | 7 | HG01257.hp2 HG01258.hp2 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.-78-5858dupA | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82793325 | ||||||
chr15:82793325
|
G | T | 1 | a0001c0001t0010g0185 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-78-5857C>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82793325 | ||||||
chr15:82793602
|
T | C | 1 | a0002c0003t0012g0363 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-78-6134A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82793602 | ||||||
chr15:82793712
|
T | C | 1 | a0001c0001t0002g0268 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-78-6244A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82793712 | ||||||
chr15:82793759
|
A | C | 1 | a0002c0003t0004g0147 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-78-6291T>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82793759 | ||||||
chr15:82793763
|
A | G | 38 | a0001c0001t0003g0354a0002c0003t0004g0004a0002c0003t0004g0147others(35): Show | 39 | HG00423.hp2 HG00544.hp1 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.-78-6295T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82793763 | ||||||
chr15:82794031
|
T | G | 16 | a0001c0001t0003g0088a0001c0002t0001g0013a0001c0002t0001g0057others(13): Show | 16 | HG00408.hp2 HG01952.hp1 HG02074.hp1 others(13): Show |
intron_variant | MODIFIER | c.-78-6563A>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82794031 | ||||||
chr15:82794048
|
T | G | 1 | a0001c0002t0016g0117 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-78-6580A>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82794048 | ||||||
chr15:82794140
|
C | G | 18 | a0001c0001t0002g0036a0001c0001t0002g0038a0001c0001t0002g0039others(15): Show | 18 | HG02965.hp2 HG02976.hp2 NA18956.hp1 others(15): Show |
intron_variant | MODIFIER | c.-78-6672G>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82794140 | ||||||
chr15:82794141
|
A | G | 16 | a0001c0001t0008g0143a0001c0001t0008g0214a0001c0001t0008g0215others(13): Show | 16 | HG01109.hp1 HG02055.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.-78-6673T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82794141 | ||||||
chr15:82794329
|
C | T | 1 | a0001c0001t0002g0216 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-78-6861G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82794329 | ||||||
chr15:82794341
|
A | G | 132 | a0001c0001t0002g0036a0001c0001t0002g0038a0001c0001t0002g0039others(129): Show | 133 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.-78-6873T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82794341 | ||||||
chr15:82794461
|
G | C | 4 | a0001c0001t0023g0009a0001c0008t0023g0286a0001c0008t0023g0287others(1): Show | 4 | HG01884.hp2 HG01891.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-78-6993C>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82794461 | ||||||
chr15:82794726
|
CT | C | 9 | a0001c0001t0002g0036a0001c0001t0002g0317a0001c0001t0014g0001others(6): Show | 12 | HG01099.hp1 HG02809.hp2 HG03139.hp1 others(9): Show |
intron_variant | MODIFIER | c.-78-7259delA | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82794726 | ||||||
chr15:82794754
|
T | G | 3 | a0001c0001t0003g0261a0001c0001t0003g0262a0001c0001t0037g0260 | 3 | HG01074.hp1 HG01934.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.-78-7286A>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82794754 | ||||||
chr15:82794786
|
G | A | 1 | a0001c0001t0012g0230 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-78-7318C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82794786 | ||||||
chr15:82795041
|
T | C | 3 | a0001c0001t0030g0288a0001c0001t0030g0289a0001c0001t0044g0164 | 3 | HG03486.hp2 HG03579.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-78-7573A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82795041 | ||||||
chr15:82795073
|
C | T | 1 | a0001c0001t0044g0164 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-78-7605G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82795073 | ||||||
chr15:82795271
|
T | C | 191 | a0001c0001t0002g0036a0001c0001t0002g0038a0001c0001t0002g0039others(188): Show | 194 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.-78-7803A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82795271 | ||||||
chr15:82795613
|
T | G | 1 | a0001c0001t0002g0121 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-78-8145A>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82795613 | ||||||
chr15:82795620
|
A | C | 24 | a0001c0001t0002g0121a0001c0001t0003g0014a0001c0001t0003g0015others(21): Show | 24 | HG00099.hp2 HG00140.hp2 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.-78-8152T>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82795620 | ||||||
chr15:82795755
|
C | A | 1 | a0001c0001t0030g0289 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-78-8287G>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82795755 | ||||||
chr15:82795831
|
C | CA | 57 | a0001c0001t0003g0354a0001c0001t0013g0167a0001c0001t0013g0168others(54): Show | 59 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.-78-8364dupT | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82795831 | ||||||
chr15:82795842
|
A | G | 2 | a0001c0001t0030g0288a0001c0001t0030g0289 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-78-8374T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82795842 | ||||||
chr15:82795860
|
T | A | 333 | a0001c0001t0002g0036a0001c0001t0002g0038a0001c0001t0002g0039others(330): Show | 340 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(337): Show |
intron_variant | MODIFIER | c.-78-8392A>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82795860 | ||||||
chr15:82796000
|
C | CT | 8 | a0001c0001t0002g0149a0001c0001t0002g0297a0001c0001t0002g0298others(5): Show | 8 | HG00597.hp1 HG02602.hp2 HG03492.hp2 others(5): Show |
intron_variant | MODIFIER | c.-78-8533dupA | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82796000 | ||||||
chr15:82796000
|
CT | C | 136 | a0001c0001t0002g0036a0001c0001t0002g0038a0001c0001t0002g0039others(133): Show | 139 | HG00544.hp2 HG00558.hp1 HG00597.hp2 others(136): Show |
intron_variant | MODIFIER | c.-78-8533delA | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82796000 | ||||||
chr15:82796000
|
CTT | C | 133 | a0001c0001t0002g0084a0001c0001t0002g0085a0001c0001t0002g0087others(130): Show | 136 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.-78-8534_-78-8533d others(4): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82796000 | ||||||
chr15:82796007
|
T | C | 8 | a0001c0001t0013g0167a0001c0001t0013g0168a0001c0001t0013g0176others(5): Show | 8 | HG02895.hp1 HG03139.hp2 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.-78-8539A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82796007 | ||||||
chr15:82796088
|
G | A | 1 | a0001c0001t0014g0001 | 4 | HG02809.hp2 HG03195.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-78-8620C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82796088 | ||||||
chr15:82796144
|
G | A | 3 | a0001c0001t0003g0172a0001c0001t0003g0173a0001c0001t0003g0208 | 3 | NA18947.hp2 NA18964.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.-78-8676C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82796144 | ||||||
chr15:82796228
|
C | T | 3 | a0001c0001t0003g0014a0001c0001t0003g0015a0001c0001t0003g0026 | 3 | HG00140.hp2 HG01099.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.-78-8760G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82796228 | ||||||
chr15:82796276
|
G | A | 1 | a0001c0001t0017g0235 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-78-8808C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82796276 | ||||||
chr15:82796296
|
C | T | 1 | a0001c0001t0002g0297 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-78-8828G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82796296 | ||||||
chr15:82796462
|
C | T | 5 | a0001c0001t0017g0236a0001c0002t0001g0055a0001c0002t0001g0060others(2): Show | 5 | HG01243.hp1 HG02257.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.-78-8994G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82796462 | ||||||
chr15:82796479
|
C | T | 23 | a0001c0001t0002g0127a0001c0001t0002g0128a0001c0001t0002g0139others(20): Show | 24 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.-78-9011G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82796479 | ||||||
chr15:82796683
|
T | C | 2 | a0001c0001t0002g0295a0001c0001t0002g0296 | 2 | HG01175.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-78-9215A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82796683 | ||||||
chr15:82796701
|
C | G | 1 | a0001c0001t0003g0181 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-78-9233G>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82796701 | ||||||
chr15:82797006
|
C | T | 80 | a0001c0001t0002g0084a0001c0001t0002g0085a0001c0001t0002g0087others(77): Show | 81 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.-79+8960G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82797006 | ||||||
chr15:82797020
|
T | TA | 7 | a0001c0001t0002g0316a0001c0001t0002g0317a0001c0001t0009g0023others(4): Show | 7 | HG00673.hp1 HG02004.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.-79+8945dupT | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82797020 | ||||||
chr15:82797020
|
TA | T | 119 | a0001c0001t0002g0127a0001c0001t0002g0128a0001c0001t0002g0139others(116): Show | 123 | HG00323.hp2 HG00558.hp1 HG00609.hp2 others(120): Show |
intron_variant | MODIFIER | c.-79+8945delT | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82797020 | ||||||
chr15:82797020
|
TAA | T | 7 | a0001c0001t0002g0274a0001c0001t0003g0186a0001c0001t0003g0233others(4): Show | 7 | HG02647.hp1 HG02896.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.-79+8944_-79+8945d others(4): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82797020 | ||||||
chr15:82797033
|
A | AC | 108 | a0001c0001t0002g0036a0001c0001t0002g0038a0001c0001t0002g0039others(105): Show | 109 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.-79+8932_-79+8933i others(3): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82797033 | ||||||
chr15:82797033
|
A | C | 1 | a0001c0002t0001g0059 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.-79+8933T>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82797033 | ||||||
chr15:82797037
|
A | AC | 23 | a0001c0001t0002g0121a0001c0001t0003g0014a0001c0001t0003g0015others(20): Show | 23 | HG00099.hp2 HG00140.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.-79+8928_-79+8929i others(3): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82797037 | ||||||
chr15:82797037
|
A | C | 111 | a0001c0001t0002g0036a0001c0001t0002g0038a0001c0001t0002g0039others(108): Show | 112 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.-79+8929T>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82797037 | ||||||
chr15:82797040
|
AAC | A | 7 | a0001c0001t0013g0167a0001c0001t0013g0168a0001c0001t0013g0176others(4): Show | 7 | HG02148.hp1 HG02895.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.-79+8924_-79+8925d others(4): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82797040 | ||||||
chr15:82797041
|
AC | A | 44 | a0001c0001t0003g0354a0002c0003t0004g0004a0002c0003t0004g0147others(41): Show | 45 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.-79+8924delG | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82797041 | ||||||
chr15:82797042
|
C | A | 143 | a0001c0001t0002g0036a0001c0001t0002g0038a0001c0001t0002g0039others(140): Show | 145 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.-79+8924G>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82797042 | ||||||
chr15:82797450
|
A | G | 1 | a0001c0001t0006g0024 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-79+8516T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82797450 | ||||||
chr15:82797536
|
C | A | 2 | a0001c0002t0001g0054a0001c0002t0001g0095 | 2 | NA18967.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.-79+8430G>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82797536 | ||||||
chr15:82797592
|
T | C | 330 | a0001c0001t0002g0036a0001c0001t0002g0038a0001c0001t0002g0039others(327): Show | 337 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(334): Show |
intron_variant | MODIFIER | c.-79+8374A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82797592 | ||||||
chr15:82797679
|
G | A | 1 | a0001c0001t0003g0210 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-79+8287C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82797679 | ||||||
chr15:82797924
|
T | C | 1 | a0001c0002t0016g0117 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-79+8042A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82797924 | ||||||
chr15:82797942
|
A | T | 1 | a0001c0001t0003g0232 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-79+8024T>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82797942 | ||||||
chr15:82797957
|
C | T | 323 | a0001c0001t0002g0036a0001c0001t0002g0038a0001c0001t0002g0039others(320): Show | 330 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(327): Show |
intron_variant | MODIFIER | c.-79+8009G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82797957 | ||||||
chr15:82798343
|
A | G | 194 | a0001c0001t0002g0036a0001c0001t0002g0038a0001c0001t0002g0039others(191): Show | 197 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.-79+7623T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82798343 | ||||||
chr15:82798509
|
A | G | 3 | a0001c0001t0030g0288a0001c0001t0030g0289a0001c0001t0044g0164 | 3 | HG03486.hp2 HG03579.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-79+7457T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82798509 | ||||||
chr15:82798737
|
C | T | 2 | a0001c0002t0001g0030a0005c0007t0033g0029 | 2 | HG03139.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-79+7229G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82798737 | ||||||
chr15:82798865
|
T | A | 52 | a0001c0001t0003g0354a0001c0001t0013g0167a0001c0001t0013g0168others(49): Show | 53 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.-79+7101A>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82798865 | ||||||
chr15:82798873
|
G | GT | 61 | a0001c0001t0002g0038a0001c0001t0002g0039a0001c0001t0002g0040others(58): Show | 64 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.-79+7092dupA | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82798873 | ||||||
chr15:82798873
|
G | GTT | 81 | a0001c0001t0002g0036a0001c0001t0003g0354a0001c0001t0006g0024others(78): Show | 83 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.-79+7091_-79+7092d others(4): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82798873 | ||||||
chr15:82798873
|
G | GTTT | 67 | a0001c0001t0002g0084a0001c0001t0002g0085a0001c0001t0002g0087others(64): Show | 68 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.-79+7090_-79+7092d others(5): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82798873 | ||||||
chr15:82798873
|
G | GTTTT | 11 | a0001c0002t0001g0012a0001c0002t0001g0055a0001c0002t0001g0056others(8): Show | 11 | HG01981.hp2 HG02055.hp2 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.-79+7089_-79+7092d others(6): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82798873 | ||||||
chr15:82798877
|
TG | T | 8 | a0001c0001t0002g0274a0001c0001t0003g0211a0001c0001t0003g0273others(5): Show | 8 | HG01257.hp1 HG02486.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-79+7088delC | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82798877 | ||||||
chr15:82798878
|
G | T | 325 | a0001c0001t0002g0036a0001c0001t0002g0038a0001c0001t0002g0039others(322): Show | 332 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(329): Show |
intron_variant | MODIFIER | c.-79+7088C>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82798878 | ||||||
chr15:82799034
|
C | T | 131 | a0001c0001t0002g0036a0001c0001t0002g0038a0001c0001t0002g0039others(128): Show | 132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.-79+6932G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82799034 | ||||||
chr15:82799122
|
C | T | 2 | a0001c0001t0002g0216a0001c0002t0001g0051 | 2 | HG03704.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-79+6844G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82799122 | ||||||
chr15:82799270
|
A | T | 1 | a0001c0001t0002g0148 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-79+6696T>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82799270 | ||||||
chr15:82799581
|
G | A | 1 | a0001c0002t0001g0105 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-79+6385C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82799581 | ||||||
chr15:82799704
|
C | T | 1 | a0001c0002t0001g0123 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-79+6262G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82799704 | ||||||
chr15:82799903
|
C | A | 135 | a0001c0001t0002g0036a0001c0001t0002g0038a0001c0001t0002g0039others(132): Show | 136 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.-79+6063G>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82799903 | ||||||
chr15:82799937
|
C | T | 2 | a0001c0001t0008g0214a0001c0001t0008g0215 | 2 | HG02451.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-79+6029G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82799937 | ||||||
chr15:82800061
|
A | G | 24 | a0001c0001t0002g0121a0001c0001t0003g0014a0001c0001t0003g0015others(21): Show | 24 | HG00099.hp2 HG00140.hp2 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.-79+5905T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82800061 | ||||||
chr15:82800180
|
C | T | 1 | a0001c0001t0021g0212 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-79+5786G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82800180 | ||||||
chr15:82800181
|
T | C | 1 | a0001c0001t0010g0145 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-79+5785A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82800181 | ||||||
chr15:82800538
|
A | C | 1 | a0001c0001t0003g0014 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-79+5428T>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82800538 | ||||||
chr15:82800678
|
C | G | 4 | a0001c0001t0023g0009a0001c0008t0023g0286a0001c0008t0023g0287others(1): Show | 4 | HG01884.hp2 HG01891.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-79+5288G>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82800678 | ||||||
chr15:82800679
|
G | A | 1 | a0001c0001t0042g0033 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-79+5287C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82800679 | ||||||
chr15:82800691
|
C | CA | 11 | a0001c0001t0002g0139a0001c0001t0002g0320a0001c0001t0003g0279others(8): Show | 11 | HG00423.hp1 HG02056.hp2 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.-79+5274dupT | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82800691 | ||||||
chr15:82800691
|
C | CAAA | 33 | a0001c0001t0003g0354a0002c0003t0004g0004a0002c0003t0004g0281others(30): Show | 34 | HG00280.hp1 HG00423.hp2 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.-79+5272_-79+5274d others(5): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82800691 | ||||||
chr15:82800691
|
C | CAAAA | 18 | a0001c0001t0013g0167a0001c0001t0013g0176a0001c0001t0013g0282others(15): Show | 19 | HG00639.hp2 HG00735.hp1 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.-79+5271_-79+5274d others(6): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82800691 | ||||||
chr15:82800691
|
C | CAAAAA | 13 | a0001c0001t0013g0168a0001c0001t0024g0374a0001c0001t0024g0375others(10): Show | 13 | HG00323.hp1 HG01070.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.-79+5270_-79+5274d others(7): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82800691 | ||||||
chr15:82800691
|
C | CAAAAAA | 78 | a0001c0001t0002g0036a0001c0001t0002g0038a0001c0001t0002g0039others(75): Show | 79 | HG00140.hp1 HG00438.hp1 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.-79+5269_-79+5274d others(8): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82800691 | ||||||
chr15:82800691
|
C | CAAAAAAA | 24 | a0001c0001t0002g0047a0001c0001t0002g0112a0001c0001t0059g0124others(21): Show | 24 | HG00408.hp1 HG00408.hp2 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.-79+5268_-79+5274d others(9): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82800691 | ||||||
chr15:82800691
|
C | CAAAAAAA others(3): Show |
5 | a0001c0001t0002g0121a0001c0001t0006g0031a0001c0001t0006g0119others(2): Show | 5 | HG01346.hp2 HG01891.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.-79+5265_-79+5274d others(12): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82800691 | ||||||
chr15:82800691
|
C | CAAAAAAA others(4): Show |
12 | a0001c0001t0003g0014a0001c0001t0003g0015a0001c0001t0006g0016others(9): Show | 12 | HG00099.hp2 HG00140.hp2 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.-79+5264_-79+5274d others(13): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82800691 | ||||||
chr15:82800691
|
C | CAAAAAAA others(5): Show |
6 | a0001c0001t0003g0026a0001c0001t0006g0024a0001c0001t0006g0025others(3): Show | 6 | HG01099.hp2 HG01106.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.-79+5263_-79+5274d others(14): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82800691 | ||||||
chr15:82800691
|
CA | C | 40 | a0001c0001t0002g0290a0001c0001t0003g0140a0001c0001t0003g0141others(37): Show | 40 | HG00544.hp2 HG00558.hp1 HG00609.hp2 others(37): Show |
intron_variant | MODIFIER | c.-79+5274delT | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82800691 | ||||||
chr15:82801017
|
C | T | 2 | a0001c0001t0009g0011a0001c0001t0009g0050 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-79+4949G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82801017 | ||||||
chr15:82801308
|
A | G | 1 | a0001c0001t0042g0033 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-79+4658T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82801308 | ||||||
chr15:82801354
|
T | C | 1 | a0001c0001t0042g0033 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-79+4612A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82801354 | ||||||
chr15:82801367
|
C | T | 21 | a0001c0001t0002g0127a0001c0001t0002g0128a0001c0001t0002g0139others(18): Show | 22 | HG00323.hp2 HG00738.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.-79+4599G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82801367 | ||||||
chr15:82801497
|
C | A | 1 | a0003c0004t0011g0032 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-79+4469G>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82801497 | ||||||
chr15:82801498
|
C | T | 1 | a0003c0004t0011g0032 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-79+4468G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82801498 | ||||||
chr15:82801573
|
C | T | 2 | a0001c0002t0001g0030a0005c0007t0033g0029 | 2 | HG03139.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-79+4393G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82801573 | ||||||
chr15:82801940
|
C | T | 18 | a0001c0001t0002g0036a0001c0001t0002g0038a0001c0001t0002g0039others(15): Show | 18 | HG02965.hp2 HG02976.hp2 NA18956.hp1 others(15): Show |
intron_variant | MODIFIER | c.-79+4026G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82801940 | ||||||
chr15:82802178
|
G | A | 4 | a0001c0001t0023g0009a0001c0008t0023g0286a0001c0008t0023g0287others(1): Show | 4 | HG01884.hp2 HG01891.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-79+3788C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82802178 | ||||||
chr15:82802249
|
C | G | 1 | a0001c0001t0003g0177 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-79+3717G>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82802249 | ||||||
chr15:82802332
|
C | G | 1 | a0003c0004t0005g0154 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-79+3634G>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82802332 | ||||||
chr15:82802332
|
C | T | 1 | a0001c0001t0013g0176 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-79+3634G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82802332 | ||||||
chr15:82802497
|
G | A | 1 | a0001c0002t0001g0123 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-79+3469C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82802497 | ||||||
chr15:82802526
|
A | G | 4 | a0001c0001t0023g0009a0001c0008t0023g0286a0001c0008t0023g0287others(1): Show | 4 | HG01884.hp2 HG01891.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-79+3440T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82802526 | ||||||
chr15:82802539
|
C | G | 4 | a0001c0001t0002g0174a0001c0001t0002g0175a0001c0001t0003g0172others(1): Show | 4 | HG02109.hp1 HG03130.hp1 NA18947.hp2 others(1): Show |
intron_variant | MODIFIER | c.-79+3427G>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82802539 | ||||||
chr15:82802747
|
C | A | 4 | a0001c0005t0011g0006a0001c0005t0011g0371a0001c0005t0011g0372others(1): Show | 5 | HG00639.hp2 HG00735.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.-79+3219G>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82802747 | ||||||
chr15:82802907
|
C | T | 1 | a0001c0002t0034g0034 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-79+3059G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82802907 | ||||||
chr15:82803173
|
T | A | 4 | a0001c0001t0023g0009a0001c0008t0023g0286a0001c0008t0023g0287others(1): Show | 4 | HG01884.hp2 HG01891.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-79+2793A>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82803173 | ||||||
chr15:82803240
|
A | G | 1 | a0003c0004t0032g0125 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-79+2726T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82803240 | ||||||
chr15:82803253
|
C | T | 3 | a0001c0001t0030g0288a0001c0001t0030g0289a0001c0001t0044g0164 | 3 | HG03486.hp2 HG03579.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-79+2713G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82803253 | ||||||
chr15:82803254
|
G | A | 4 | a0001c0005t0011g0006a0001c0005t0011g0371a0001c0005t0011g0372others(1): Show | 5 | HG00639.hp2 HG00735.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.-79+2712C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82803254 | ||||||
chr15:82803424
|
T | C | 3 | a0001c0001t0030g0288a0001c0001t0030g0289a0001c0001t0044g0164 | 3 | HG03486.hp2 HG03579.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-79+2542A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82803424 | ||||||
chr15:82803597
|
A | G | 335 | a0001c0001t0002g0036a0001c0001t0002g0038a0001c0001t0002g0039others(332): Show | 342 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(339): Show |
intron_variant | MODIFIER | c.-79+2369T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82803597 | ||||||
chr15:82803655
|
G | C | 2 | a0003c0004t0005g0154a0003c0004t0005g0155 | 2 | HG02109.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-79+2311C>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82803655 | ||||||
chr15:82803755
|
T | C | 124 | a0001c0001t0002g0036a0001c0001t0002g0038a0001c0001t0002g0039others(121): Show | 125 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.-79+2211A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82803755 | ||||||
chr15:82803861
|
C | T | 1 | a0002c0003t0004g0171 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-79+2105G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82803861 | ||||||
chr15:82803990
|
A | G | 4 | a0001c0005t0011g0006a0001c0005t0011g0371a0001c0005t0011g0372others(1): Show | 5 | HG00639.hp2 HG00735.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.-79+1976T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82803990 | ||||||
chr15:82804024
|
A | C | 1 | a0001c0001t0003g0170 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-79+1942T>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82804024 | ||||||
chr15:82804026
|
G | T | 1 | a0001c0001t0003g0170 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-79+1940C>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82804026 | ||||||
chr15:82804031
|
A | T | 1 | a0001c0001t0003g0170 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-79+1935T>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82804031 | ||||||
chr15:82804032
|
G | C | 1 | a0001c0001t0003g0170 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-79+1934C>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82804032 | ||||||
chr15:82804038
|
G | T | 1 | a0001c0001t0003g0170 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-79+1928C>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82804038 | ||||||
chr15:82804043
|
T | G | 1 | a0001c0001t0003g0170 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-79+1923A>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82804043 | ||||||
chr15:82804044
|
G | A | 1 | a0001c0001t0003g0170 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-79+1922C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82804044 | ||||||
chr15:82804046
|
T | C | 1 | a0001c0001t0003g0170 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-79+1920A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82804046 | ||||||
chr15:82804048
|
T | C | 1 | a0001c0001t0003g0170 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-79+1918A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82804048 | ||||||
chr15:82804049
|
T | C | 1 | a0001c0001t0003g0170 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-79+1917A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82804049 | ||||||
chr15:82804050
|
G | A | 1 | a0001c0001t0003g0170 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-79+1916C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82804050 | ||||||
chr15:82804055
|
T | A | 1 | a0001c0001t0003g0170 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-79+1911A>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82804055 | ||||||
chr15:82804063
|
T | G | 1 | a0001c0001t0003g0170 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-79+1903A>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82804063 | ||||||
chr15:82804070
|
G | C | 1 | a0001c0001t0003g0170 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-79+1896C>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82804070 | ||||||
chr15:82804075
|
C | G | 1 | a0001c0001t0003g0170 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-79+1891G>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82804075 | ||||||
chr15:82804077
|
A | G | 1 | a0001c0001t0003g0170 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-79+1889T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82804077 | ||||||
chr15:82804078
|
C | G | 1 | a0001c0001t0003g0170 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-79+1888G>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82804078 | ||||||
chr15:82804079
|
C | T | 1 | a0001c0001t0003g0170 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-79+1887G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82804079 | ||||||
chr15:82804082
|
A | T | 1 | a0001c0001t0003g0170 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-79+1884T>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82804082 | ||||||
chr15:82804087
|
C | T | 1 | a0001c0001t0003g0170 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-79+1879G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82804087 | ||||||
chr15:82804093
|
C | G | 1 | a0001c0001t0003g0170 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-79+1873G>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82804093 | ||||||
chr15:82804095
|
T | A | 1 | a0001c0001t0003g0170 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-79+1871A>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82804095 | ||||||
chr15:82804096
|
G | T | 1 | a0001c0001t0003g0170 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-79+1870C>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82804096 | ||||||
chr15:82804217
|
C | T | 1 | a0001c0001t0006g0031 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-79+1749G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82804217 | ||||||
chr15:82804237
|
G | A | 1 | a0001c0001t0003g0321 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-79+1729C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82804237 | ||||||
chr15:82804266
|
C | T | 1 | a0001c0001t0006g0031 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-79+1700G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82804266 | ||||||
chr15:82804275
|
G | A | 1 | a0001c0001t0002g0322 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-79+1691C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82804275 | ||||||
chr15:82804305
|
T | C | 1 | a0001c0001t0011g0007 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-79+1661A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82804305 | ||||||
chr15:82804513
|
C | T | 1 | a0001c0001t0003g0169 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-79+1453G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82804513 | ||||||
chr15:82804615
|
C | A | 1 | a0001c0001t0059g0124 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-79+1351G>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82804615 | ||||||
chr15:82804625
|
C | T | 2 | a0001c0002t0001g0030a0005c0007t0033g0029 | 2 | HG03139.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-79+1341G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82804625 | ||||||
chr15:82804790
|
C | T | 3 | a0001c0001t0013g0167a0001c0001t0013g0168a0001c0001t0043g0166 | 3 | HG02895.hp1 HG03139.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-79+1176G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82804790 | ||||||
chr15:82804796
|
C | T | 1 | a0001c0001t0011g0007 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-79+1170G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82804796 | ||||||
chr15:82804837
|
A | G | 1 | a0001c0001t0027g0323 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-79+1129T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82804837 | ||||||
chr15:82805087
|
A | T | 1 | a0001c0002t0001g0163 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-79+879T>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82805087 | ||||||
chr15:82805088
|
G | T | 1 | a0001c0002t0001g0163 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-79+878C>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82805088 | ||||||
chr15:82805089
|
G | T | 1 | a0001c0002t0001g0163 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-79+877C>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82805089 | ||||||
chr15:82805090
|
C | T | 1 | a0001c0002t0001g0163 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-79+876G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82805090 | ||||||
chr15:82805092
|
T | A | 1 | a0001c0002t0001g0163 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-79+874A>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82805092 | ||||||
chr15:82805100
|
A | T | 1 | a0001c0001t0010g0165 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.-79+866T>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82805100 | ||||||
chr15:82805104
|
G | A | 1 | a0001c0002t0001g0163 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-79+862C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82805104 | ||||||
chr15:82805106
|
A | T | 1 | a0001c0002t0001g0163 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-79+860T>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82805106 | ||||||
chr15:82805108
|
C | T | 1 | a0001c0002t0001g0163 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-79+858G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82805108 | ||||||
chr15:82805109
|
C | T | 1 | a0001c0002t0001g0163 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-79+857G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82805109 | ||||||
chr15:82805110
|
C | T | 1 | a0001c0002t0001g0163 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-79+856G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82805110 | ||||||
chr15:82805112
|
G | A | 1 | a0001c0002t0001g0163 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-79+854C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82805112 | ||||||
chr15:82805113
|
T | A | 1 | a0001c0002t0001g0163 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-79+853A>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82805113 | ||||||
chr15:82805114
|
G | T | 1 | a0001c0002t0001g0163 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-79+852C>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82805114 | ||||||
chr15:82805115
|
C | A | 1 | a0001c0002t0001g0163 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-79+851G>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82805115 | ||||||
chr15:82805119
|
A | T | 1 | a0001c0002t0001g0163 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-79+847T>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82805119 | ||||||
chr15:82805120
|
C | G | 1 | a0001c0002t0001g0163 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-79+846G>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82805120 | ||||||
chr15:82805127
|
A | T | 1 | a0001c0002t0001g0163 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-79+839T>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82805127 | ||||||
chr15:82805129
|
G | A | 1 | a0001c0002t0001g0163 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-79+837C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82805129 | ||||||
chr15:82805131
|
C | T | 1 | a0001c0002t0001g0163 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-79+835G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82805131 | ||||||
chr15:82805132
|
C | T | 1 | a0001c0002t0001g0163 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-79+834G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82805132 | ||||||
chr15:82805133
|
C | A | 1 | a0001c0002t0001g0163 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-79+833G>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82805133 | ||||||
chr15:82805134
|
C | A | 1 | a0001c0002t0001g0163 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-79+832G>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82805134 | ||||||
chr15:82805135
|
C | T | 1 | a0001c0002t0001g0163 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-79+831G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82805135 | ||||||
chr15:82805136
|
A | T | 1 | a0001c0002t0001g0163 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-79+830T>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82805136 | ||||||
chr15:82805139
|
A | C | 1 | a0001c0001t0044g0164 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-79+827T>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82805139 | ||||||
chr15:82805139
|
A | T | 1 | a0001c0002t0001g0163 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-79+827T>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82805139 | ||||||
chr15:82805140
|
A | AT | 40 | a0001c0001t0002g0127a0001c0001t0002g0128a0001c0001t0002g0139others(37): Show | 42 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.-79+825dupA | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82805140 | ||||||
chr15:82805140
|
A | ATT | 99 | a0001c0001t0002g0036a0001c0001t0002g0038a0001c0001t0002g0039others(96): Show | 100 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.-79+824_-79+825dup others(2): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82805140 | ||||||
chr15:82805140
|
A | ATTT | 24 | a0001c0001t0003g0014a0001c0001t0003g0015a0001c0001t0003g0026others(21): Show | 25 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.-79+823_-79+825dup others(3): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82805140 | ||||||
chr15:82805140
|
AT | A | 48 | a0001c0001t0003g0329a0001c0001t0003g0330a0001c0001t0003g0354others(45): Show | 48 | HG00280.hp1 HG00423.hp2 HG00733.hp2 others(45): Show |
intron_variant | MODIFIER | c.-79+825delA | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82805140 | ||||||
chr15:82805311
|
G | A | 1 | a0002c0003t0004g0370 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-79+655C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82805311 | ||||||
chr15:82805358
|
T | A | 375 | a0001c0001t0002g0005a0001c0001t0002g0036a0001c0001t0002g0038others(372): Show | 383 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(380): Show |
intron_variant | MODIFIER | c.-79+608A>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82805358 | ||||||
chr15:82805714
|
A | G | 1 | a0001c0001t0011g0007 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-79+252T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82805714 | ||||||
chr15:82805860
|
A | G | 4 | a0001c0005t0011g0006a0001c0005t0011g0371a0001c0005t0011g0372others(1): Show | 5 | HG00639.hp2 HG00735.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.-79+106T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82805860 | ||||||
chr15:82805889
|
T | C | 4 | a0001c0005t0011g0006a0001c0005t0011g0371a0001c0005t0011g0372others(1): Show | 5 | HG00639.hp2 HG00735.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.-79+77A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82805889 |