geneid | 26173 |
---|---|
ensemblid | ENSG00000164880.16 |
hgncid | 24555 |
symbol | INTS1 |
name | integrator complex subunit 1 |
refseq_nuc | NM_001080453.3 |
refseq_prot | NP_001073922.2 |
ensembl_nuc | ENST00000404767.8 |
ensembl_prot | ENSP00000385722.3 |
mane_status | MANE Select |
chr | chr7 |
start | 1470277 |
end | 1504389 |
strand | - |
ver | v1.2 |
region | chr7:1470277-1504389 |
region5000 | chr7:1465277-1509389 |
regionname0 | INTS1_chr7_1470277_1504389 |
regionname5000 | INTS1_chr7_1465277_1509389 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 2190 | 294 | 81 | 66 | 103 | 14 | 28 | 63 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0002 | 0/0 | 2190 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0003 | 0/0 | 2190 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0004 | 0/0 | 2190 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0005 | 0/0 | 2190 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0006 | 0/0 | 2175 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0007 | 0/0 | 2190 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0008 | 0/0 | 2190 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0009 | 0/0 | 2190 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0010 | 0/0 | 2190 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0011 | 0/0 | 2190 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0012 | 0/0 | 2190 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0013 | 0/0 | 2190 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0014 | 0/0 | 2190 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0015 | 0/0 | 2190 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0016 | 0/0 | 2190 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0017 | 0/0 | 2190 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0018 | 0/0 | 2190 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0019 | 0/0 | 2190 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 6573 | 129 | 32 | 22 | 57 | 8 | 9 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
c0002 | 1/0 | 6573 | 103 | 14 | 34 | 37 | 4 | 13 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
c0003 | 0/0 | 6573 | 8 | 6 | 2 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
c0004 | 0/0 | 6573 | 7 | 1 | 0 | 6 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
c0005 | 0/0 | 6573 | 6 | 4 | 1 | 0 | 1 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
c0006 | 0/0 | 6573 | 4 | 3 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
c0007 | 0/0 | 6573 | 3 | 3 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
c0008 | 0/0 | 6573 | 3 | 0 | 0 | 0 | 0 | 3 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
c0009 | 0/0 | 6573 | 3 | 3 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
c0010 | 0/0 | 6573 | 3 | 3 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
c0011 | 0/0 | 6573 | 3 | 1 | 2 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
c0012 | 0/0 | 6573 | 2 | 0 | 0 | 0 | 0 | 2 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
c0013 | 0/0 | 6573 | 2 | 0 | 2 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
c0014 | 0/0 | 6573 | 2 | 2 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
c0015 | 0/0 | 6573 | 2 | 2 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
c0016 | 0/0 | 6573 | 2 | 0 | 1 | 0 | 1 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
c0017 | 0/0 | 6573 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
c0018 | 0/0 | 6573 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
c0019 | 0/0 | 6573 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
c0020 | 0/0 | 6573 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
c0021 | 0/0 | 6573 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
c0022 | 0/0 | 6573 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
c0023 | 0/0 | 6573 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
c0024 | 0/0 | 6573 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
c0025 | 0/0 | 6573 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
c0026 | 0/0 | 6573 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
c0027 | 0/0 | 6573 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
c0028 | 0/0 | 6573 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
c0029 | 0/0 | 6573 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
c0030 | 0/0 | 6573 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
c0031 | 0/0 | 6573 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
c0032 | 0/0 | 6528 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
c0033 | 0/0 | 6573 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
c0034 | 0/0 | 6573 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
c0035 | 0/0 | 6573 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
c0036 | 0/0 | 6573 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
c0037 | 0/0 | 6573 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
c0038 | 0/0 | 6573 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
c0039 | 0/0 | 6573 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
c0040 | 0/0 | 6573 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
c0041 | 0/0 | 6573 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
c0042 | 0/0 | 6573 | 1 | 0 | 0 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
c0043 | 0/0 | 6573 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
c0044 | 0/0 | 6573 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
c0045 | 0/0 | 6573 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
c0046 | 0/0 | 6573 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
c0047 | 0/0 | 6573 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
c0048 | 0/0 | 6573 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
c0049 | 0/0 | 6573 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
c0050 | 0/0 | 6573 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 409 | 169 | 60 | 28 | 61 | 8 | 11 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
t0002 | 1/0 | 409 | 118 | 23 | 37 | 39 | 4 | 14 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
t0003 | 0/0 | 409 | 9 | 6 | 0 | 0 | 0 | 3 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
t0004 | 0/0 | 409 | 9 | 0 | 0 | 9 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
t0005 | 0/0 | 406 | 4 | 3 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
t0006 | 0/0 | 409 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
t0007 | 0/0 | 409 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
t0008 | 0/0 | 409 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
t0009 | 0/0 | 409 | 1 | 0 | 0 | 0 | 1 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
t0010 | 0/0 | 406 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
t0011 | 0/0 | 409 | 1 | 0 | 0 | 0 | 1 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
t0012 | 0/0 | 409 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 9 | 0 | 4 | 5 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0002 | 0/0 | 6 | 0 | 3 | 0 | 2 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0003 | 0/0 | 6 | 1 | 4 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0004 | 0/0 | 6 | 1 | 4 | 0 | 1 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0005 | 0/0 | 6 | 0 | 3 | 3 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0006 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0008 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0011 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0013 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0020 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0021 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0024 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0028 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0040 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0085 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0152 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 6573 | 129 | 32 | 22 | 57 | 8 | 9 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0001c0002 | 1/0 | 6573 | 103 | 14 | 34 | 37 | 4 | 13 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0001c0003 | 0/0 | 6573 | 8 | 6 | 2 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0001c0004 | 0/0 | 6573 | 7 | 1 | 0 | 6 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0001c0005 | 0/0 | 6573 | 6 | 4 | 1 | 0 | 1 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0001c0006 | 0/0 | 6573 | 4 | 3 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0001c0008 | 0/0 | 6573 | 3 | 0 | 0 | 0 | 0 | 3 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0001c0009 | 0/0 | 6573 | 3 | 3 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0001c0010 | 0/0 | 6573 | 3 | 3 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0001c0011 | 0/0 | 6573 | 3 | 1 | 2 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0001c0012 | 0/0 | 6573 | 2 | 0 | 0 | 0 | 0 | 2 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0001c0013 | 0/0 | 6573 | 2 | 0 | 2 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0001c0016 | 0/0 | 6573 | 2 | 0 | 1 | 0 | 1 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0001c0018 | 0/0 | 6573 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0001c0019 | 0/0 | 6573 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0001c0020 | 0/0 | 6573 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0001c0021 | 0/0 | 6573 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0001c0026 | 0/0 | 6573 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0001c0027 | 0/0 | 6573 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0001c0028 | 0/0 | 6573 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0001c0031 | 0/0 | 6573 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0001c0034 | 0/0 | 6573 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0001c0035 | 0/0 | 6573 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0001c0036 | 0/0 | 6573 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0001c0037 | 0/0 | 6573 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0001c0038 | 0/0 | 6573 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0001c0039 | 0/0 | 6573 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0001c0041 | 0/0 | 6573 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0001c0042 | 0/0 | 6573 | 1 | 0 | 0 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0001c0047 | 0/0 | 6573 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0001c0048 | 0/0 | 6573 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0001c0049 | 0/0 | 6573 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0002c0007 | 0/0 | 6573 | 3 | 3 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0003c0015 | 0/0 | 6573 | 2 | 2 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0004c0014 | 0/0 | 6573 | 2 | 2 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0005c0030 | 0/0 | 6573 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0006c0032 | 0/0 | 6528 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0007c0022 | 0/0 | 6573 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0008c0033 | 0/0 | 6573 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0009c0046 | 0/0 | 6573 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0010c0044 | 0/0 | 6573 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0011c0023 | 0/0 | 6573 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0012c0040 | 0/0 | 6573 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0013c0043 | 0/0 | 6573 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0014c0024 | 0/0 | 6573 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0015c0045 | 0/0 | 6573 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0016c0025 | 0/0 | 6573 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0017c0029 | 0/0 | 6573 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0018c0050 | 0/0 | 6573 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0019c0017 | 0/0 | 6573 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 6981 | 119 | 31 | 22 | 49 | 7 | 9 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0001c0001t0002 | 0/0 | 6981 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0001c0001t0004 | 0/0 | 6981 | 7 | 0 | 0 | 7 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0001c0001t0009 | 0/0 | 6981 | 1 | 0 | 0 | 0 | 1 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0001c0001t0012 | 0/0 | 6981 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0001c0002t0002 | 1/0 | 6981 | 101 | 14 | 32 | 37 | 4 | 13 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0001c0002t0006 | 0/0 | 6981 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0001c0002t0007 | 0/0 | 6981 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0001c0003t0001 | 0/0 | 6981 | 8 | 6 | 2 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0001c0004t0001 | 0/0 | 6981 | 7 | 1 | 0 | 6 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0001c0005t0001 | 0/0 | 6981 | 6 | 4 | 1 | 0 | 1 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0001c0006t0005 | 0/0 | 6978 | 4 | 3 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0001c0008t0003 | 0/0 | 6981 | 3 | 0 | 0 | 0 | 0 | 3 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0001c0009t0001 | 0/0 | 6981 | 3 | 3 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0001c0010t0001 | 0/0 | 6981 | 3 | 3 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0001c0011t0001 | 0/0 | 6981 | 3 | 1 | 2 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0001c0012t0001 | 0/0 | 6981 | 1 | 0 | 0 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0001c0012t0002 | 0/0 | 6981 | 1 | 0 | 0 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0001c0013t0002 | 0/0 | 6981 | 2 | 0 | 2 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0001c0016t0001 | 0/0 | 6981 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0001c0016t0011 | 0/0 | 6981 | 1 | 0 | 0 | 0 | 1 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0001c0018t0003 | 0/0 | 6981 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0001c0019t0003 | 0/0 | 6981 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0001c0020t0003 | 0/0 | 6981 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0001c0021t0002 | 0/0 | 6981 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0001c0026t0002 | 0/0 | 6981 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0001c0027t0002 | 0/0 | 6981 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0001c0028t0002 | 0/0 | 6981 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0001c0031t0001 | 0/0 | 6981 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0001c0034t0002 | 0/0 | 6981 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0001c0035t0001 | 0/0 | 6981 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0001c0036t0010 | 0/0 | 6978 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0001c0037t0001 | 0/0 | 6981 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0001c0038t0001 | 0/0 | 6981 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0001c0039t0001 | 0/0 | 6981 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0001c0041t0001 | 0/0 | 6981 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0001c0042t0001 | 0/0 | 6981 | 1 | 0 | 0 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0001c0047t0001 | 0/0 | 6981 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0001c0048t0001 | 0/0 | 6981 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0001c0049t0002 | 0/0 | 6981 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0002c0007t0003 | 0/0 | 6981 | 3 | 3 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0003c0015t0001 | 0/0 | 6981 | 2 | 2 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0004c0014t0002 | 0/0 | 6981 | 2 | 2 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0005c0030t0001 | 0/0 | 6981 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0006c0032t0004 | 0/0 | 6936 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0007c0022t0002 | 0/0 | 6981 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0008c0033t0008 | 0/0 | 6981 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0009c0046t0001 | 0/0 | 6981 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0010c0044t0001 | 0/0 | 6981 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0011c0023t0002 | 0/0 | 6981 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0012c0040t0004 | 0/0 | 6981 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0013c0043t0001 | 0/0 | 6981 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0014c0024t0002 | 0/0 | 6981 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0015c0045t0001 | 0/0 | 6981 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0016c0025t0002 | 0/0 | 6981 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0017c0029t0002 | 0/0 | 6981 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0018c0050t0001 | 0/0 | 6981 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
a0019c0017t0001 | 0/0 | 6981 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | copy fasta | chr7 | 1465277 | 1509389 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 9 | 0 | 4 | 5 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0005 | 0/0 | 6 | 0 | 3 | 3 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0006 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0152 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0004g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0004g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0004g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0004g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0004g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0009g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0001t0012g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0002 | 0/0 | 6 | 0 | 3 | 0 | 2 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0003 | 0/0 | 6 | 1 | 4 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0004 | 0/0 | 6 | 1 | 4 | 0 | 1 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0008 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0011 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0013 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0020 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0021 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0024 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0085 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0006g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0002t0007g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0003t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0003t0001g0040 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0003t0001g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0003t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0003t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0004t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0004t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0004t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0004t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0004t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0005t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0005t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0005t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0005t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0005t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0005t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0006t0005g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0006t0005g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0006t0005g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0008t0003g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0008t0003g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0009t0001g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0009t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0010t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0010t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0011t0001g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0011t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0012t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0012t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0013t0002g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0016t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0016t0011g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0018t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0019t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0020t0003g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0021t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0026t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0027t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0028t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0031t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0034t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0035t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0036t0010g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0037t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0038t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0039t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0041t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0042t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0047t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0048t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0001c0049t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0002c0007t0003g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0002c0007t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0003c0015t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0004c0014t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0004c0014t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0005c0030t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0006c0032t0004g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0007c0022t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0008c0033t0008g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0009c0046t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0010c0044t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0011c0023t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0012c0040t0004g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0013c0043t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0014c0024t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0015c0045t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0016c0025t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0017c0029t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0018c0050t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
a0019c0017t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0170 | EUR | GBR | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0158 | EUR | GBR | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0127 | EUR | GBR | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG00140 | hp2 | a0001 | c0002 | t0002 | g0004 | EUR | GBR | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0028 | EUR | FIN | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG00280 | hp2 | a0001 | c0005 | t0001 | g0140 | EUR | FIN | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG00408 | hp1 | a0001 | c0001 | t0004 | g0036 | EAS | CHS | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG00408 | hp2 | a0001 | c0004 | t0001 | g0015 | EAS | CHS | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG00423 | hp1 | a0001 | c0002 | t0002 | g0061 | EAS | CHS | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG00438 | hp2 | a0001 | c0002 | t0002 | g0012 | EAS | CHS | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG00544 | hp2 | a0001 | c0002 | t0002 | g0091 | EAS | CHS | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG00558 | hp1 | a0001 | c0002 | t0002 | g0009 | EAS | CHS | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG00558 | hp2 | a0001 | c0001 | t0004 | g0038 | EAS | CHS | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG00597 | hp1 | a0001 | c0002 | t0002 | g0064 | EAS | CHS | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG00597 | hp2 | a0001 | c0001 | t0004 | g0038 | EAS | CHS | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | CHS | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG00639 | hp1 | a0001 | c0011 | t0001 | g0041 | AMR | PUR | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG00639 | hp2 | a0001 | c0002 | t0002 | g0004 | AMR | PUR | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG00642 | hp2 | a0017 | c0029 | t0002 | g0096 | AMR | PUR | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG00673 | hp1 | a0001 | c0002 | t0002 | g0010 | EAS | CHS | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | CHS | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG00733 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG00735 | hp2 | a0001 | c0002 | t0007 | g0099 | AMR | PUR | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01069 | hp1 | a0001 | c0002 | t0002 | g0013 | AMR | PUR | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01071 | hp2 | a0001 | c0002 | t0002 | g0013 | AMR | PUR | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01074 | hp1 | a0001 | c0016 | t0001 | g0162 | AMR | PUR | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01074 | hp2 | a0001 | c0002 | t0002 | g0008 | AMR | PUR | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01081 | hp2 | a0001 | c0011 | t0001 | g0041 | AMR | PUR | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01099 | hp1 | a0001 | c0002 | t0002 | g0024 | AMR | PUR | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01109 | hp1 | a0001 | c0002 | t0002 | g0098 | AMR | PUR | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01109 | hp2 | a0001 | c0027 | t0002 | g0103 | AMR | PUR | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01167 | hp1 | a0001 | c0002 | t0002 | g0025 | AMR | PUR | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01167 | hp2 | a0001 | c0002 | t0002 | g0011 | AMR | PUR | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01168 | hp1 | a0001 | c0002 | t0002 | g0062 | AMR | PUR | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01168 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01169 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01169 | hp2 | a0001 | c0002 | t0002 | g0025 | AMR | PUR | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01175 | hp1 | a0001 | c0002 | t0002 | g0013 | AMR | PUR | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01175 | hp2 | a0001 | c0005 | t0001 | g0139 | AMR | PUR | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01243 | hp1 | a0001 | c0006 | t0005 | g0228 | AMR | PUR | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01243 | hp2 | a0001 | c0003 | t0001 | g0199 | AMR | PUR | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01255 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | CLM | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01255 | hp2 | a0001 | c0003 | t0001 | g0040 | AMR | CLM | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01257 | hp2 | a0001 | c0013 | t0002 | g0022 | AMR | CLM | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01258 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | CLM | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01258 | hp2 | a0001 | c0013 | t0002 | g0022 | AMR | CLM | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01346 | hp1 | a0001 | c0002 | t0002 | g0065 | AMR | CLM | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01358 | hp1 | a0001 | c0002 | t0002 | g0050 | AMR | CLM | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01358 | hp2 | a0001 | c0002 | t0002 | g0084 | AMR | CLM | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01361 | hp1 | a0001 | c0002 | t0002 | g0086 | AMR | CLM | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01496 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | CLM | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | CLM | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0126 | EUR | IBS | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0137 | EUR | IBS | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01516 | hp1 | a0001 | c0002 | t0002 | g0002 | EUR | IBS | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01516 | hp2 | a0001 | c0001 | t0009 | g0155 | EUR | IBS | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01884 | hp1 | a0001 | c0005 | t0001 | g0214 | AFR | ACB | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01884 | hp2 | a0001 | c0002 | t0002 | g0003 | AFR | ACB | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01891 | hp1 | a0001 | c0002 | t0002 | g0026 | AFR | ACB | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01934 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | PEL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01934 | hp2 | a0001 | c0002 | t0002 | g0052 | AMR | PEL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01943 | hp1 | a0001 | c0002 | t0006 | g0066 | AMR | PEL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01952 | hp1 | a0016 | c0025 | t0002 | g0081 | AMR | PEL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01952 | hp2 | a0001 | c0002 | t0002 | g0053 | AMR | PEL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01975 | hp1 | a0001 | c0002 | t0002 | g0080 | AMR | PEL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01975 | hp2 | a0001 | c0002 | t0002 | g0004 | AMR | PEL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | PEL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01981 | hp1 | a0001 | c0002 | t0002 | g0004 | AMR | PEL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01993 | hp1 | a0001 | c0002 | t0002 | g0051 | AMR | PEL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01993 | hp2 | a0001 | c0002 | t0002 | g0004 | AMR | PEL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02004 | hp1 | a0001 | c0002 | t0002 | g0055 | AMR | PEL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02015 | hp1 | a0001 | c0002 | t0002 | g0020 | EAS | KHV | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02027 | hp1 | a0001 | c0002 | t0002 | g0078 | EAS | KHV | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | KHV | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02040 | hp2 | a0007 | c0022 | t0002 | g0063 | EAS | KHV | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | ACB | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02056 | hp1 | a0001 | c0002 | t0002 | g0070 | EAS | KHV | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02056 | hp2 | a0006 | c0032 | t0004 | g0205 | EAS | KHV | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02071 | hp1 | a0001 | c0001 | t0004 | g0165 | EAS | KHV | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02071 | hp2 | a0001 | c0002 | t0002 | g0090 | EAS | KHV | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02074 | hp2 | a0001 | c0001 | t0004 | g0173 | EAS | KHV | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02083 | hp2 | a0001 | c0002 | t0002 | g0068 | EAS | KHV | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02129 | hp1 | a0001 | c0004 | t0001 | g0015 | EAS | KHV | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02129 | hp2 | a0001 | c0001 | t0004 | g0036 | EAS | KHV | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | KHV | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02132 | hp2 | a0001 | c0002 | t0002 | g0092 | EAS | KHV | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02145 | hp1 | a0001 | c0002 | t0002 | g0019 | AFR | ACB | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02145 | hp2 | a0008 | c0033 | t0008 | g0118 | AFR | ACB | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02155 | hp1 | a0001 | c0002 | t0002 | g0008 | EAS | CDX | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | CDX | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | CDX | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | CDX | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02257 | hp1 | a0001 | c0002 | t0002 | g0004 | AFR | ACB | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02257 | hp2 | a0001 | c0003 | t0001 | g0197 | AFR | ACB | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02258 | hp1 | a0001 | c0002 | t0002 | g0011 | AFR | ACB | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02258 | hp2 | a0001 | c0021 | t0002 | g0089 | AFR | ACB | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02280 | hp1 | a0001 | c0010 | t0001 | g0030 | AFR | ACB | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02280 | hp2 | a0001 | c0018 | t0003 | g0108 | AFR | ACB | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02293 | hp1 | a0001 | c0002 | t0002 | g0097 | AMR | PEL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02451 | hp1 | a0014 | c0024 | t0002 | g0067 | AFR | ACB | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02451 | hp2 | a0001 | c0010 | t0001 | g0145 | AFR | ACB | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02572 | hp1 | a0001 | c0006 | t0005 | g0227 | AFR | GWD | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02572 | hp2 | a0001 | c0003 | t0001 | g0042 | AFR | GWD | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | GWD | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02615 | hp2 | a0001 | c0002 | t0002 | g0093 | AFR | GWD | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | GWD | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | GWD | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02630 | hp1 | a0001 | c0006 | t0005 | g0044 | AFR | GWD | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02647 | hp1 | a0011 | c0023 | t0002 | g0087 | AFR | GWD | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02647 | hp2 | a0001 | c0047 | t0001 | g0179 | AFR | GWD | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02698 | hp1 | a0001 | c0042 | t0001 | g0204 | SAS | PJL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02698 | hp2 | a0001 | c0002 | t0002 | g0071 | SAS | PJL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02717 | hp1 | a0001 | c0006 | t0005 | g0044 | AFR | GWD | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02717 | hp2 | a0001 | c0048 | t0001 | g0192 | AFR | GWD | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02723 | hp1 | a0002 | c0007 | t0003 | g0027 | AFR | GWD | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | GWD | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02738 | hp1 | a0001 | c0008 | t0003 | g0018 | SAS | PJL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02738 | hp2 | a0001 | c0012 | t0001 | g0117 | SAS | PJL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02818 | hp1 | a0001 | c0002 | t0002 | g0019 | AFR | GWD | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02818 | hp2 | a0001 | c0003 | t0001 | g0042 | AFR | GWD | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02886 | hp1 | a0019 | c0017 | t0001 | g0114 | AFR | GWD | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02886 | hp2 | a0001 | c0035 | t0001 | g0143 | AFR | GWD | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02895 | hp1 | a0001 | c0009 | t0001 | g0043 | AFR | GWD | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02895 | hp2 | a0001 | c0003 | t0001 | g0029 | AFR | GWD | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02897 | hp1 | a0001 | c0005 | t0001 | g0116 | AFR | GWD | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02897 | hp2 | a0001 | c0003 | t0001 | g0029 | AFR | GWD | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | ESN | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02922 | hp2 | a0001 | c0005 | t0001 | g0215 | AFR | ESN | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | ESN | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ESN | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02970 | hp1 | a0001 | c0002 | t0002 | g0011 | AFR | ESN | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | ESN | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG03017 | hp1 | a0001 | c0002 | t0002 | g0021 | SAS | PJL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG03017 | hp2 | a0001 | c0002 | t0002 | g0059 | SAS | PJL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG03041 | hp1 | a0001 | c0036 | t0010 | g0226 | AFR | GWD | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG03041 | hp2 | a0003 | c0015 | t0001 | g0035 | AFR | GWD | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG03098 | hp1 | a0001 | c0020 | t0003 | g0110 | AFR | MSL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | MSL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG03130 | hp1 | a0001 | c0009 | t0001 | g0043 | AFR | ESN | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG03130 | hp2 | a0002 | c0007 | t0003 | g0107 | AFR | ESN | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG03139 | hp1 | a0001 | c0049 | t0002 | g0106 | AFR | ESN | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG03139 | hp2 | a0003 | c0015 | t0001 | g0035 | AFR | ESN | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ESN | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG03209 | hp1 | a0001 | c0002 | t0002 | g0088 | AFR | MSL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | MSL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG03225 | hp1 | a0001 | c0011 | t0001 | g0210 | AFR | MSL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG03225 | hp2 | a0001 | c0003 | t0001 | g0040 | AFR | MSL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG03239 | hp1 | a0001 | c0002 | t0002 | g0002 | SAS | PJL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG03239 | hp2 | a0001 | c0002 | t0002 | g0077 | SAS | PJL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG03453 | hp1 | a0009 | c0046 | t0001 | g0178 | AFR | MSL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG03453 | hp2 | a0001 | c0031 | t0001 | g0123 | AFR | MSL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG03486 | hp1 | a0001 | c0001 | t0002 | g0105 | AFR | MSL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG03486 | hp2 | a0001 | c0038 | t0001 | g0115 | AFR | MSL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG03492 | hp1 | a0001 | c0002 | t0002 | g0047 | SAS | PJL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG03492 | hp2 | a0001 | c0008 | t0003 | g0018 | SAS | PJL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG03540 | hp2 | a0001 | c0037 | t0001 | g0198 | AFR | GWD | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | MSL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | MSL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG03654 | hp2 | a0001 | c0002 | t0002 | g0021 | SAS | PJL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | STU | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG03688 | hp2 | a0001 | c0002 | t0002 | g0069 | SAS | STU | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | PJL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG03704 | hp2 | a0001 | c0002 | t0002 | g0003 | SAS | PJL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG03831 | hp1 | a0001 | c0008 | t0003 | g0048 | SAS | BEB | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0211 | SAS | BEB | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | BEB | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0212 | SAS | BEB | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG04184 | hp1 | a0001 | c0012 | t0002 | g0056 | SAS | BEB | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0200 | SAS | BEB | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG04199 | hp1 | a0001 | c0002 | t0002 | g0046 | SAS | STU | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG04199 | hp2 | a0001 | c0002 | t0002 | g0060 | SAS | STU | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | YRI | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18522 | hp2 | a0010 | c0044 | t0001 | g0183 | AFR | YRI | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18612 | hp1 | a0001 | c0002 | t0002 | g0007 | EAS | CHB | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | CHB | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18747 | hp2 | a0001 | c0002 | t0002 | g0073 | EAS | CHB | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18906 | hp1 | a0001 | c0034 | t0002 | g0045 | AFR | YRI | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18906 | hp2 | a0004 | c0014 | t0002 | g0058 | AFR | YRI | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18939 | hp1 | a0001 | c0002 | t0002 | g0101 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18939 | hp2 | a0015 | c0045 | t0001 | g0182 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18945 | hp2 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18947 | hp1 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18947 | hp2 | a0001 | c0004 | t0001 | g0015 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18950 | hp1 | a0005 | c0030 | t0001 | g0142 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18954 | hp1 | a0001 | c0028 | t0002 | g0094 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18954 | hp2 | a0001 | c0039 | t0001 | g0151 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18964 | hp1 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18964 | hp2 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18967 | hp1 | a0001 | c0001 | t0012 | g0230 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18967 | hp2 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18969 | hp2 | a0001 | c0002 | t0002 | g0079 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18971 | hp1 | a0001 | c0001 | t0004 | g0174 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18971 | hp2 | a0001 | c0002 | t0002 | g0054 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18973 | hp1 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18977 | hp1 | a0001 | c0002 | t0002 | g0012 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18982 | hp1 | a0001 | c0002 | t0002 | g0023 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18983 | hp1 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18984 | hp1 | a0018 | c0050 | t0001 | g0213 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18984 | hp2 | a0001 | c0002 | t0002 | g0074 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18985 | hp1 | a0012 | c0040 | t0004 | g0181 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18988 | hp1 | a0001 | c0002 | t0002 | g0076 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18997 | hp2 | a0001 | c0002 | t0002 | g0023 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18998 | hp1 | a0001 | c0004 | t0001 | g0147 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA18998 | hp2 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA19000 | hp2 | a0001 | c0004 | t0001 | g0193 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA19007 | hp1 | a0001 | c0002 | t0002 | g0072 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA19009 | hp2 | a0001 | c0002 | t0002 | g0075 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA19010 | hp1 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA19030 | hp1 | a0001 | c0010 | t0001 | g0030 | AFR | LWK | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | LWK | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | LWK | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | LWK | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA19055 | hp1 | a0001 | c0002 | t0002 | g0012 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA19068 | hp2 | a0001 | c0041 | t0001 | g0128 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA19074 | hp1 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA19074 | hp2 | a0001 | c0004 | t0001 | g0148 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA19090 | hp2 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA19091 | hp1 | a0013 | c0043 | t0001 | g0112 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA19240 | hp1 | a0001 | c0009 | t0001 | g0220 | AFR | YRI | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA19240 | hp2 | a0001 | c0019 | t0003 | g0109 | AFR | YRI | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | ASW | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA20129 | hp2 | a0001 | c0026 | t0002 | g0104 | AFR | ASW | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA20752 | hp1 | a0001 | c0016 | t0011 | g0229 | EUR | TSI | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA20752 | hp2 | a0001 | c0002 | t0002 | g0083 | EUR | TSI | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0185 | EUR | TSI | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA20805 | hp2 | a0001 | c0002 | t0002 | g0002 | EUR | TSI | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA20905 | hp1 | a0001 | c0002 | t0002 | g0082 | SAS | GIH | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA20905 | hp2 | a0001 | c0002 | t0002 | g0102 | SAS | GIH | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | CLM | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG01123 | hp2 | a0001 | c0002 | t0002 | g0020 | AMR | CLM | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | ACB | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02486 | hp1 | a0001 | c0002 | t0002 | g0026 | AFR | ACB | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02486 | hp2 | a0001 | c0002 | t0002 | g0049 | AFR | ACB | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | ACB | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG03471 | hp1 | a0001 | c0002 | t0002 | g0024 | AFR | MSL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG03471 | hp2 | a0001 | c0002 | t0002 | g0095 | AFR | MSL | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | USA | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
HG06807 | hp2 | a0004 | c0014 | t0002 | g0057 | AFR | USA | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA20300 | hp1 | a0002 | c0007 | t0003 | g0027 | AFR | USA | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA20300 | hp2 | a0001 | c0004 | t0001 | g0149 | AFR | USA | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA21309 | hp1 | a0001 | c0002 | t0002 | g0100 | AFR | LWK | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
NA21309 | hp2 | a0001 | c0005 | t0001 | g0216 | AFR | LWK | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0152 | REF | REF | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0002 | g0085 | REF | REF | INTS1_chr7_1465277_1509389 | INTS1 | chr7 | 1465277 | 1509389 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:1472297
|
G | A | 1 | a0011 | 1 | HG02647.hp1 | missense_variant | MODERATE | c.6160C>T | p.Leu2054Phe | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 44/48 | 6268/6981 | 6160/6573 | 2054/2190 | chr7 | 1472297 | ||
chr7:1473172
|
G | C | 1 | a0012 | 1 | NA18985.hp1 | missense_variant | MODERATE | c.5970C>G | p.Phe1990Leu | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 43/48 | 6078/6981 | 5970/6573 | 1990/2190 | chr7 | 1473172 | ||
chr7:1474299
|
G | A | 1 | a0013 | 1 | NA19091.hp1 | missense_variant | MODERATE | c.5698C>T | p.Arg1900Trp | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 41/48 | 5806/6981 | 5698/6573 | 1900/2190 | chr7 | 1474299 | ||
chr7:1474801
|
G | A | 1 | a0014 | 1 | HG02451.hp1 | missense_variant | MODERATE | c.5540C>T | p.Ala1847Val | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 40/48 | 5648/6981 | 5540/6573 | 1847/2190 | chr7 | 1474801 | ||
chr7:1475998
|
G | A | 1 | a0002 | 3 | HG02723.hp1 HG03130.hp2 NA20300.hp1 |
missense_variant | MODERATE | c.5452C>T | p.Pro1818Ser | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 39/48 | 5560/6981 | 5452/6573 | 1818/2190 | chr7 | 1475998 | ||
chr7:1477771
|
G | A | 1 | a0010 | 1 | NA18522.hp2 | missense_variant | MODERATE | c.4796C>T | p.Pro1599Leu | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 34/48 | 4904/6981 | 4796/6573 | 1599/2190 | chr7 | 1477771 | ||
chr7:1477864
|
G | A | 1 | a0015 | 1 | NA18939.hp2 | missense_variant | MODERATE | c.4703C>T | p.Ala1568Val | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 34/48 | 4811/6981 | 4703/6573 | 1568/2190 | chr7 | 1477864 | ||
chr7:1479480
|
G | A | 1 | a0009 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.4279C>T | p.Arg1427Cys | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 31/48 | 4387/6981 | 4279/6573 | 1427/2190 | chr7 | 1479480 | ||
chr7:1479642
|
G | C | 1 | a0008 | 1 | HG02145.hp2 | missense_variant | MODERATE | c.4117C>G | p.Pro1373Ala | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 31/48 | 4225/6981 | 4117/6573 | 1373/2190 | chr7 | 1479642 | ||
chr7:1480360
|
C | T | 1 | a0003 | 2 | HG03041.hp2 HG03139.hp2 |
missense_variant | MODERATE | c.4031G>A | p.Arg1344Gln | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 30/48 | 4139/6981 | 4031/6573 | 1344/2190 | chr7 | 1480360 | ||
chr7:1482686
|
G | A | 1 | a0016 | 1 | HG01952.hp1 | missense_variant | MODERATE | c.3563C>T | p.Ala1188Val | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 27/48 | 3671/6981 | 3563/6573 | 1188/2190 | chr7 | 1482686 | ||
chr7:1486639
|
C | T | 1 | a0007 | 1 | HG02040.hp2 | missense_variant | MODERATE | c.2962G>A | p.Val988Met | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 22/48 | 3070/6981 | 2962/6573 | 988/2190 | chr7 | 1486639 | ||
chr7:1497225
|
CTGCTTGA others(38): Show |
C | 1 | a0006 | 1 | HG02056.hp2 | disruptive_inframe_deletion | MODERATE | c.1470_1514delCTACCT others(39): Show |
p.Asp490_Gln505delin others(4): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 11/48 | 1622/6981 | 1470/6573 | 490/2190 | chr7 | 1497225 | ||
chr7:1498981
|
G | T | 1 | a0006 | 1 | HG02056.hp2 | missense_variant | MODERATE | c.1131C>A | p.Asn377Lys | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 8/48 | 1239/6981 | 1131/6573 | 377/2190 | chr7 | 1498981 | ||
chr7:1499003
|
T | C | 1 | a0004 | 2 | HG06807.hp2 NA18906.hp2 |
missense_variant | MODERATE | c.1109A>G | p.Lys370Arg | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 8/48 | 1217/6981 | 1109/6573 | 370/2190 | chr7 | 1499003 | ||
chr7:1499626
|
T | C | 1 | a0017 | 1 | HG00642.hp2 | missense_variant | MODERATE | c.691A>G | p.Ile231Val | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 6/48 | 799/6981 | 691/6573 | 231/2190 | chr7 | 1499626 | ||
chr7:1500280
|
C | G | 1 | a0005 | 1 | NA18950.hp1 | missense_variant | MODERATE | c.436G>C | p.Val146Leu | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 4/48 | 544/6981 | 436/6573 | 146/2190 | chr7 | 1500280 | ||
chr7:1503179
|
G | C | 1 | a0018 | 1 | NA18984.hp1 | missense_variant | MODERATE | c.71C>G | p.Pro24Arg | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/48 | 179/6981 | 71/6573 | 24/2190 | chr7 | 1503179 | ||
chr7:1503951
|
C | T | 1 | a0019 | 1 | HG02886.hp1 | missense_variant | MODERATE | c.10G>A | p.Ala4Thr | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 2/48 | 118/6981 | 10/6573 | 4/2190 | chr7 | 1503951 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:1471195
|
G | A | 1 | a0001c0009 | 3 | HG02895.hp1 HG03130.hp1 NA19240.hp1 |
synonymous_variant | LOW | c.6285C>T | p.Ala2095Ala | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 46/48 | 6393/6981 | 6285/6573 | 2095/2190 | chr7 | 1471195 | ||
chr7:1471198
|
C | T | 1 | a0001c0042 | 1 | HG02698.hp1 | synonymous_variant | LOW | c.6282G>A | p.Ser2094Ser | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 46/48 | 6390/6981 | 6282/6573 | 2094/2190 | chr7 | 1471198 | ||
chr7:1471637
|
C | T | 3 | a0001c0018a0001c0019a0002c0007 | 5 | HG02280.hp2 HG02723.hp1 HG03130.hp2 others(2): Show |
synonymous_variant | LOW | c.6189G>A | p.Leu2063Leu | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 45/48 | 6297/6981 | 6189/6573 | 2063/2190 | chr7 | 1471637 | ||
chr7:1472307
|
G | A | 1 | a0001c0009 | 3 | HG02895.hp1 HG03130.hp1 NA19240.hp1 |
synonymous_variant | LOW | c.6150C>T | p.Tyr2050Tyr | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 44/48 | 6258/6981 | 6150/6573 | 2050/2190 | chr7 | 1472307 | ||
chr7:1473571
|
C | T | 1 | a0001c0041 | 1 | NA19068.hp2 | synonymous_variant | LOW | c.5952G>A | p.Pro1984Pro | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 42/48 | 6060/6981 | 5952/6573 | 1984/2190 | chr7 | 1473571 | ||
chr7:1473591
|
G | A | 1 | a0001c0006 | 4 | HG01243.hp1 HG02572.hp1 HG02630.hp1 others(1): Show |
synonymous_variant | LOW | c.5932C>T | p.Leu1978Leu | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 42/48 | 6040/6981 | 5932/6573 | 1978/2190 | chr7 | 1473591 | ||
chr7:1474170
|
G | A | 1 | a0001c0008 | 3 | HG02738.hp1 HG03492.hp2 HG03831.hp1 |
splice_region_variant&synonymous_variant | LOW | c.5827C>T | p.Leu1943Leu | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 41/48 | 5935/6981 | 5827/6573 | 1943/2190 | chr7 | 1474170 | ||
chr7:1474728
|
C | T | 2 | a0001c0003a0019c0017 | 9 | HG01243.hp2 HG01255.hp2 HG02257.hp2 others(6): Show |
synonymous_variant | LOW | c.5613G>A | p.Val1871Val | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 40/48 | 5721/6981 | 5613/6573 | 1871/2190 | chr7 | 1474728 | ||
chr7:1476825
|
G | T | 1 | a0008c0033 | 1 | HG02145.hp2 | synonymous_variant | LOW | c.5032C>A | p.Arg1678Arg | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 36/48 | 5140/6981 | 5032/6573 | 1678/2190 | chr7 | 1476825 | ||
chr7:1477607
|
G | A | 1 | a0001c0008 | 3 | HG02738.hp1 HG03492.hp2 HG03831.hp1 |
synonymous_variant | LOW | c.4881C>T | p.Pro1627Pro | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 35/48 | 4989/6981 | 4881/6573 | 1627/2190 | chr7 | 1477607 | ||
chr7:1478499
|
C | T | 2 | a0001c0026a0001c0027 | 2 | HG01109.hp2 NA20129.hp2 |
synonymous_variant | LOW | c.4497G>A | p.Gly1499Gly | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 33/48 | 4605/6981 | 4497/6573 | 1499/2190 | chr7 | 1478499 | ||
chr7:1478790
|
C | A | 2 | a0001c0026a0001c0027 | 2 | HG01109.hp2 NA20129.hp2 |
synonymous_variant | LOW | c.4425G>T | p.Gly1475Gly | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 32/48 | 4533/6981 | 4425/6573 | 1475/2190 | chr7 | 1478790 | ||
chr7:1478865
|
G | A | 1 | a0001c0009 | 3 | HG02895.hp1 HG03130.hp1 NA19240.hp1 |
synonymous_variant | LOW | c.4350C>T | p.Thr1450Thr | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 32/48 | 4458/6981 | 4350/6573 | 1450/2190 | chr7 | 1478865 | ||
chr7:1480896
|
G | A | 2 | a0001c0006a0001c0036 | 5 | HG01243.hp1 HG02572.hp1 HG02630.hp1 others(2): Show |
synonymous_variant | LOW | c.3888C>T | p.Arg1296Arg | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 29/48 | 3996/6981 | 3888/6573 | 1296/2190 | chr7 | 1480896 | ||
chr7:1482706
|
G | A | 4 | a0001c0006a0001c0009a0001c0034others(1): Show | 9 | HG01243.hp1 HG02572.hp1 HG02630.hp1 others(6): Show |
splice_region_variant&synonymous_variant | LOW | c.3543C>T | p.Ala1181Ala | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 27/48 | 3651/6981 | 3543/6573 | 1181/2190 | chr7 | 1482706 | ||
chr7:1483815
|
G | A | 1 | a0001c0035 | 1 | HG02886.hp2 | synonymous_variant | LOW | c.3468C>T | p.Ser1156Ser | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 26/48 | 3576/6981 | 3468/6573 | 1156/2190 | chr7 | 1483815 | ||
chr7:1484093
|
C | A | 2 | a0001c0009a0001c0047 | 4 | HG02647.hp2 HG02895.hp1 HG03130.hp1 others(1): Show |
synonymous_variant | LOW | c.3339G>T | p.Ser1113Ser | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 25/48 | 3447/6981 | 3339/6573 | 1113/2190 | chr7 | 1484093 | ||
chr7:1484093
|
C | T | 1 | a0001c0018 | 1 | HG02280.hp2 | synonymous_variant | LOW | c.3339G>A | p.Ser1113Ser | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 25/48 | 3447/6981 | 3339/6573 | 1113/2190 | chr7 | 1484093 | ||
chr7:1484099
|
G | A | 5 | a0001c0008a0001c0018a0001c0019others(2): Show | 9 | HG02280.hp2 HG02723.hp1 HG02738.hp1 others(6): Show |
synonymous_variant | LOW | c.3333C>T | p.Ala1111Ala | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 25/48 | 3441/6981 | 3333/6573 | 1111/2190 | chr7 | 1484099 | ||
chr7:1484117
|
C | T | 1 | a0003c0015 | 2 | HG03041.hp2 HG03139.hp2 |
synonymous_variant | LOW | c.3315G>A | p.Ser1105Ser | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 25/48 | 3423/6981 | 3315/6573 | 1105/2190 | chr7 | 1484117 | ||
chr7:1485323
|
G | A | 1 | a0001c0013 | 2 | HG01257.hp2 HG01258.hp2 |
synonymous_variant | LOW | c.3123C>T | p.Ser1041Ser | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 23/48 | 3231/6981 | 3123/6573 | 1041/2190 | chr7 | 1485323 | ||
chr7:1485334
|
G | A | 1 | a0001c0036 | 1 | HG03041.hp1 | synonymous_variant | LOW | c.3112C>T | p.Leu1038Leu | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 23/48 | 3220/6981 | 3112/6573 | 1038/2190 | chr7 | 1485334 | ||
chr7:1485461
|
C | T | 1 | a0012c0040 | 1 | NA18985.hp1 | synonymous_variant | LOW | c.2985G>A | p.Ser995Ser | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 23/48 | 3093/6981 | 2985/6573 | 995/2190 | chr7 | 1485461 | ||
chr7:1486655
|
G | A | 1 | a0001c0006 | 4 | HG01243.hp1 HG02572.hp1 HG02630.hp1 others(1): Show |
synonymous_variant | LOW | c.2946C>T | p.Ser982Ser | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 22/48 | 3054/6981 | 2946/6573 | 982/2190 | chr7 | 1486655 | ||
chr7:1486664
|
G | A | 1 | a0001c0016 | 2 | HG01074.hp1 NA20752.hp1 |
synonymous_variant | LOW | c.2937C>T | p.Leu979Leu | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 22/48 | 3045/6981 | 2937/6573 | 979/2190 | chr7 | 1486664 | ||
chr7:1487024
|
C | T | 1 | a0001c0026 | 1 | NA20129.hp2 | synonymous_variant | LOW | c.2724G>A | p.Gln908Gln | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 21/48 | 2832/6981 | 2724/6573 | 908/2190 | chr7 | 1487024 | ||
chr7:1487939
|
C | T | 1 | a0001c0021 | 1 | HG02258.hp2 | synonymous_variant | LOW | c.2337G>A | p.Pro779Pro | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 19/48 | 2445/6981 | 2337/6573 | 779/2190 | chr7 | 1487939 | ||
chr7:1489670
|
C | T | 1 | a0001c0018 | 1 | HG02280.hp2 | synonymous_variant | LOW | c.2178G>A | p.Pro726Pro | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 17/48 | 2286/6981 | 2178/6573 | 726/2190 | chr7 | 1489670 | ||
chr7:1493084
|
C | T | 1 | a0001c0039 | 1 | NA18954.hp2 | synonymous_variant | LOW | c.2091G>A | p.Gly697Gly | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/48 | 2199/6981 | 2091/6573 | 697/2190 | chr7 | 1493084 | ||
chr7:1493877
|
A | G | 40 | a0001c0001a0001c0003a0001c0004others(37): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
synonymous_variant | LOW | c.1945T>C | p.Leu649Leu | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 15/48 | 2053/6981 | 1945/6573 | 649/2190 | chr7 | 1493877 | ||
chr7:1496202
|
C | T | 1 | a0001c0004 | 7 | HG00408.hp2 HG02129.hp1 NA18947.hp2 others(4): Show |
synonymous_variant | LOW | c.1665G>A | p.Ala555Ala | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 12/48 | 1773/6981 | 1665/6573 | 555/2190 | chr7 | 1496202 | ||
chr7:1497267
|
G | A | 2 | a0001c0026a0001c0027 | 2 | HG01109.hp2 NA20129.hp2 |
synonymous_variant | LOW | c.1473C>T | p.Tyr491Tyr | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 11/48 | 1581/6981 | 1473/6573 | 491/2190 | chr7 | 1497267 | ||
chr7:1498430
|
G | A | 1 | a0001c0048 | 1 | HG02717.hp2 | synonymous_variant | LOW | c.1407C>T | p.Ser469Ser | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 10/48 | 1515/6981 | 1407/6573 | 469/2190 | chr7 | 1498430 | ||
chr7:1498481
|
G | A | 1 | a0001c0006 | 4 | HG01243.hp1 HG02572.hp1 HG02630.hp1 others(1): Show |
synonymous_variant | LOW | c.1356C>T | p.Ser452Ser | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 10/48 | 1464/6981 | 1356/6573 | 452/2190 | chr7 | 1498481 | ||
chr7:1498511
|
G | A | 3 | a0001c0003a0001c0037a0019c0017 | 10 | HG01243.hp2 HG01255.hp2 HG02257.hp2 others(7): Show |
synonymous_variant | LOW | c.1326C>T | p.Ile442Ile | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 10/48 | 1434/6981 | 1326/6573 | 442/2190 | chr7 | 1498511 | ||
chr7:1498538
|
C | T | 1 | a0001c0010 | 3 | HG02280.hp1 HG02451.hp2 NA19030.hp1 |
synonymous_variant | LOW | c.1299G>A | p.Ala433Ala | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 10/48 | 1407/6981 | 1299/6573 | 433/2190 | chr7 | 1498538 | ||
chr7:1498760
|
G | A | 1 | a0001c0049 | 1 | HG03139.hp1 | synonymous_variant | LOW | c.1230C>T | p.Ile410Ile | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 9/48 | 1338/6981 | 1230/6573 | 410/2190 | chr7 | 1498760 | ||
chr7:1498790
|
G | A | 1 | a0001c0038 | 1 | HG03486.hp2 | synonymous_variant | LOW | c.1200C>T | p.Ser400Ser | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 9/48 | 1308/6981 | 1200/6573 | 400/2190 | chr7 | 1498790 | ||
chr7:1498978
|
G | A | 19 | a0001c0001a0001c0004a0001c0010others(16): Show | 159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
synonymous_variant | LOW | c.1134C>T | p.Pro378Pro | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 8/48 | 1242/6981 | 1134/6573 | 378/2190 | chr7 | 1498978 | ||
chr7:1499302
|
G | A | 1 | a0001c0028 | 1 | NA18954.hp1 | synonymous_variant | LOW | c.903C>T | p.Ile301Ile | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 7/48 | 1011/6981 | 903/6573 | 301/2190 | chr7 | 1499302 | ||
chr7:1499335
|
C | T | 1 | a0001c0031 | 1 | HG03453.hp2 | synonymous_variant | LOW | c.870G>A | p.Thr290Thr | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 7/48 | 978/6981 | 870/6573 | 290/2190 | chr7 | 1499335 | ||
chr7:1499582
|
G | A | 1 | a0001c0011 | 3 | HG00639.hp1 HG01081.hp2 HG03225.hp1 |
synonymous_variant | LOW | c.735C>T | p.His245His | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 6/48 | 843/6981 | 735/6573 | 245/2190 | chr7 | 1499582 | ||
chr7:1503061
|
G | A | 32 | a0001c0001a0001c0003a0001c0004others(29): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
synonymous_variant | LOW | c.189C>T | p.Ala63Ala | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/48 | 297/6981 | 189/6573 | 63/2190 | chr7 | 1503061 | ||
chr7:1503178
|
T | C | 31 | a0001c0001a0001c0003a0001c0004others(28): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
synonymous_variant | LOW | c.72A>G | p.Pro24Pro | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/48 | 180/6981 | 72/6573 | 24/2190 | chr7 | 1503178 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:1470290
|
G | A | 1 | a0001c0002t0006 | 1 | HG01943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*287C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 48/48 | 287 | chr7 | 1470290 | |||||
chr7:1470356
|
CAGA | C | 2 | a0001c0006t0005a0001c0036t0010 | 5 | HG01243.hp1 HG02572.hp1 HG02630.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*218_*220delTCT | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 48/48 | 218 | chr7 | 1470356 | |||||
chr7:1470376
|
G | A | 1 | a0001c0006t0005 | 4 | HG01243.hp1 HG02572.hp1 HG02630.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*201C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 48/48 | 201 | chr7 | 1470376 | |||||
chr7:1470465
|
C | T | 1 | a0001c0001t0009 | 1 | HG01516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*112G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 48/48 | 112 | chr7 | 1470465 | |||||
chr7:1470479
|
C | T | 1 | a0008c0033t0008 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*98G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 48/48 | 98 | chr7 | 1470479 | |||||
chr7:1470536
|
G | A | 3 | a0001c0001t0004a0006c0032t0004a0012c0040t0004 | 9 | HG00408.hp1 HG00558.hp2 HG00597.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*41C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 48/48 | 41 | chr7 | 1470536 | |||||
chr7:1470541
|
G | A | 1 | a0001c0002t0007 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*36C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 48/48 | 36 | chr7 | 1470541 | |||||
chr7:1470546
|
G | A | 5 | a0001c0008t0003a0001c0018t0003a0001c0019t0003others(2): Show | 9 | HG02280.hp2 HG02723.hp1 HG02738.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*31C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 48/48 | 31 | chr7 | 1470546 | |||||
chr7:1504345
|
C | A | 35 | a0001c0001t0001a0001c0001t0004a0001c0001t0009others(32): Show | 187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
5_prime_UTR_variant | MODIFIER | c.-64G>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 1/48 | 385 | chr7 | 1504345 | |||||
chr7:1504349
|
G | A | 1 | a0001c0016t0011 | 1 | NA20752.hp1 | 5_prime_UTR_variant | MODIFIER | c.-68C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 1/48 | 389 | chr7 | 1504349 | |||||
chr7:1504386
|
T | A | 1 | a0001c0001t0012 | 1 | NA18967.hp1 | 5_prime_UTR_variant | MODIFIER | c.-105A>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 1/48 | 426 | chr7 | 1504386 | |||||
chr7:1504388
|
T | A | 1 | a0001c0001t0012 | 1 | NA18967.hp1 | 5_prime_UTR_variant | MODIFIER | c.-107A>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 1/48 | 428 | chr7 | 1504388 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:1470726
|
G | A | 1 | a0001c0027t0002g0103 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.6458-34C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 47/47 | chr7 | 1470726 | ||||||
chr7:1470760
|
G | A | 2 | a0001c0008t0003g0018a0001c0008t0003g0048 | 3 | HG02738.hp1 HG03492.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.6458-68C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 47/47 | chr7 | 1470760 | ||||||
chr7:1470774
|
C | T | 1 | a0001c0009t0001g0220 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.6457+72G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 47/47 | chr7 | 1470774 | ||||||
chr7:1470810
|
G | A | 1 | a0001c0002t0002g0061 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.6457+36C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 47/47 | chr7 | 1470810 | ||||||
chr7:1471021
|
G | T | 4 | a0001c0018t0003g0108a0001c0019t0003g0109a0002c0007t0003g0027others(1): Show | 5 | HG02280.hp2 HG02723.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.6348-66C>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 46/47 | chr7 | 1471021 | ||||||
chr7:1471024
|
C | T | 2 | a0001c0009t0001g0043a0001c0009t0001g0220 | 3 | HG02895.hp1 HG03130.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.6348-69G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 46/47 | chr7 | 1471024 | ||||||
chr7:1471325
|
A | G | 1 | a0014c0024t0002g0067 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.6256-101T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 45/47 | chr7 | 1471325 | ||||||
chr7:1471429
|
G | A | 1 | a0010c0044t0001g0183 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.6255+142C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 45/47 | chr7 | 1471429 | ||||||
chr7:1471446
|
C | T | 1 | a0001c0002t0002g0023 | 2 | NA18982.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.6255+125G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 45/47 | chr7 | 1471446 | ||||||
chr7:1471648
|
C | G | 1 | a0001c0001t0001g0206 | 1 | HG02723.hp2 | splice_region_variant&intron_variant | LOW | c.6185-7G>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 44/47 | chr7 | 1471648 | ||||||
chr7:1471648
|
CAGAG | C | 3 | a0001c0006t0005g0044a0001c0006t0005g0227a0001c0006t0005g0228 | 4 | HG01243.hp1 HG02572.hp1 HG02630.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.6185-11_6185-8delC others(3): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 44/47 | chr7 | 1471648 | ||||||
chr7:1471683
|
G | T | 2 | a0001c0016t0001g0162a0001c0016t0011g0229 | 2 | HG01074.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.6185-42C>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 44/47 | chr7 | 1471683 | ||||||
chr7:1471795
|
C | A | 1 | a0001c0002t0002g0076 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.6185-154G>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 44/47 | chr7 | 1471795 | ||||||
chr7:1471816
|
C | T | 1 | a0001c0038t0001g0115 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.6185-175G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 44/47 | chr7 | 1471816 | ||||||
chr7:1471857
|
C | T | 1 | a0001c0002t0002g0050 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.6185-216G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 44/47 | chr7 | 1471857 | ||||||
chr7:1471859
|
C | T | 1 | a0001c0001t0004g0174 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.6185-218G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 44/47 | chr7 | 1471859 | ||||||
chr7:1471868
|
A | G | 154 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(151): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.6185-227T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 44/47 | chr7 | 1471868 | ||||||
chr7:1471901
|
G | A | 3 | a0001c0006t0005g0044a0001c0006t0005g0227a0001c0006t0005g0228 | 4 | HG01243.hp1 HG02572.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.6185-260C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 44/47 | chr7 | 1471901 | ||||||
chr7:1471928
|
C | T | 2 | a0001c0026t0002g0104a0001c0027t0002g0103 | 2 | HG01109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.6185-287G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 44/47 | chr7 | 1471928 | ||||||
chr7:1471953
|
A | G | 157 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(154): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.6185-312T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 44/47 | chr7 | 1471953 | ||||||
chr7:1471962
|
C | T | 1 | a0001c0002t0002g0071 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.6184+311G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 44/47 | chr7 | 1471962 | ||||||
chr7:1471984
|
T | C | 26 | a0001c0003t0001g0029a0001c0003t0001g0040a0001c0003t0001g0042others(23): Show | 32 | HG01109.hp2 HG01243.hp1 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.6184+289A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 44/47 | chr7 | 1471984 | ||||||
chr7:1472022
|
C | T | 5 | a0001c0006t0005g0044a0001c0006t0005g0227a0001c0006t0005g0228others(2): Show | 6 | HG01243.hp1 HG02145.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.6184+251G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 44/47 | chr7 | 1472022 | ||||||
chr7:1472162
|
G | A | 2 | a0001c0004t0001g0148a0001c0004t0001g0193 | 2 | NA19000.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.6184+111C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 44/47 | chr7 | 1472162 | ||||||
chr7:1472183
|
G | T | 2 | a0001c0001t0001g0201a0001c0001t0001g0202 | 2 | HG00621.hp1 HG02027.hp2 |
intron_variant | MODIFIER | c.6184+90C>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 44/47 | chr7 | 1472183 | ||||||
chr7:1472197
|
G | A | 3 | a0001c0009t0001g0043a0001c0009t0001g0220a0001c0034t0002g0045 | 4 | HG02895.hp1 HG03130.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.6184+76C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 44/47 | chr7 | 1472197 | ||||||
chr7:1472211
|
G | T | 1 | a0001c0002t0002g0047 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.6184+62C>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 44/47 | chr7 | 1472211 | ||||||
chr7:1472248
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.6184+25C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 44/47 | chr7 | 1472248 | ||||||
chr7:1472252
|
G | A | 1 | a0001c0036t0010g0226 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.6184+21C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 44/47 | chr7 | 1472252 | ||||||
chr7:1472417
|
C | G | 1 | a0001c0001t0001g0154 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.6071-31G>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 43/47 | chr7 | 1472417 | ||||||
chr7:1472418
|
G | C | 1 | a0001c0001t0001g0154 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.6071-32C>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 43/47 | chr7 | 1472418 | ||||||
chr7:1472544
|
C | T | 1 | a0001c0005t0001g0215 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.6071-158G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 43/47 | chr7 | 1472544 | ||||||
chr7:1472569
|
A | C | 1 | a0001c0005t0001g0215 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.6071-183T>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 43/47 | chr7 | 1472569 | ||||||
chr7:1472634
|
A | G | 1 | a0001c0001t0001g0175 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.6071-248T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 43/47 | chr7 | 1472634 | ||||||
chr7:1472666
|
C | T | 6 | a0001c0003t0001g0029a0001c0003t0001g0040a0001c0003t0001g0042others(3): Show | 9 | HG01243.hp2 HG01255.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.6071-280G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 43/47 | chr7 | 1472666 | ||||||
chr7:1472760
|
G | T | 1 | a0001c0001t0001g0211 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.6070+312C>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 43/47 | chr7 | 1472760 | ||||||
chr7:1472785
|
G | A | 1 | a0001c0041t0001g0128 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.6070+287C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 43/47 | chr7 | 1472785 | ||||||
chr7:1472794
|
C | CTGGTGGA | 17 | a0001c0005t0001g0116a0001c0005t0001g0214a0001c0005t0001g0215others(14): Show | 19 | HG01109.hp2 HG01884.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.6070+271_6070+277d others(9): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 43/47 | chr7 | 1472794 | ||||||
chr7:1472847
|
G | T | 7 | a0001c0003t0001g0029a0001c0003t0001g0040a0001c0003t0001g0042others(4): Show | 10 | HG01243.hp2 HG01255.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.6070+225C>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 43/47 | chr7 | 1472847 | ||||||
chr7:1472851
|
G | A | 7 | a0001c0003t0001g0029a0001c0003t0001g0040a0001c0003t0001g0042others(4): Show | 10 | HG01243.hp2 HG01255.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.6070+221C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 43/47 | chr7 | 1472851 | ||||||
chr7:1472855
|
C | T | 1 | a0008c0033t0008g0118 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.6070+217G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 43/47 | chr7 | 1472855 | ||||||
chr7:1472905
|
G | T | 17 | a0001c0001t0001g0017a0001c0001t0001g0039a0001c0001t0001g0133others(14): Show | 21 | HG01891.hp2 HG02055.hp2 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.6070+167C>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 43/47 | chr7 | 1472905 | ||||||
chr7:1472966
|
C | CATCGGGA others(11): Show |
1 | a0001c0001t0001g0154 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.6070+88_6070+105du others(19): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 43/47 | chr7 | 1472966 | ||||||
chr7:1473002
|
C | CA | 21 | a0001c0003t0001g0029a0001c0003t0001g0040a0001c0003t0001g0042others(18): Show | 27 | HG01243.hp1 HG01243.hp2 HG01255.hp2 others(24): Show |
intron_variant | MODIFIER | c.6070+69_6070+70ins others(1): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 43/47 | chr7 | 1473002 | ||||||
chr7:1473187
|
G | A | 3 | a0001c0001t0001g0033a0001c0001t0001g0138a0001c0001t0001g0195 | 4 | HG00738.hp2 HG01070.hp2 HG01071.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.5958-3C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 42/47 | chr7 | 1473187 | ||||||
chr7:1473324
|
C | T | 6 | a0001c0008t0003g0018a0001c0008t0003g0048a0001c0019t0003g0109others(3): Show | 8 | HG02723.hp1 HG02738.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.5958-140G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 42/47 | chr7 | 1473324 | ||||||
chr7:1473342
|
G | A | 3 | a0001c0001t0001g0032a0001c0001t0001g0150a0001c0001t0001g0206 | 4 | HG02723.hp2 HG02922.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.5958-158C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 42/47 | chr7 | 1473342 | ||||||
chr7:1473394
|
G | A | 1 | a0008c0033t0008g0118 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.5957+172C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 42/47 | chr7 | 1473394 | ||||||
chr7:1473454
|
G | A | 2 | a0001c0001t0001g0160a0001c0001t0001g0208 | 2 | HG03704.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.5957+112C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 42/47 | chr7 | 1473454 | ||||||
chr7:1473479
|
C | T | 3 | a0001c0001t0001g0152a0001c0001t0001g0194a0001c0001t0001g0225 | 3 | HG00733.hp2 HG01978.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.5957+87G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 42/47 | chr7 | 1473479 | ||||||
chr7:1473480
|
G | A | 1 | a0001c0001t0001g0014 | 3 | HG00438.hp1 HG02015.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.5957+86C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 42/47 | chr7 | 1473480 | ||||||
chr7:1473709
|
G | A | 1 | a0001c0035t0001g0143 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.5830-16C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 41/47 | chr7 | 1473709 | ||||||
chr7:1473733
|
G | A | 4 | a0001c0006t0005g0044a0001c0006t0005g0227a0001c0006t0005g0228others(1): Show | 5 | HG01243.hp1 HG02572.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.5830-40C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 41/47 | chr7 | 1473733 | ||||||
chr7:1473775
|
C | T | 1 | a0001c0034t0002g0045 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.5830-82G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 41/47 | chr7 | 1473775 | ||||||
chr7:1473980
|
C | T | 2 | a0001c0005t0001g0214a0001c0005t0001g0216 | 2 | HG01884.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.5829+188G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 41/47 | chr7 | 1473980 | ||||||
chr7:1474143
|
G | C | 4 | a0001c0005t0001g0215a0001c0021t0002g0089a0001c0026t0002g0104others(1): Show | 4 | HG01109.hp2 HG02258.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.5829+25C>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 41/47 | chr7 | 1474143 | ||||||
chr7:1474391
|
C | T | 1 | a0001c0034t0002g0045 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.5637-31G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 40/47 | chr7 | 1474391 | ||||||
chr7:1474413
|
C | G | 6 | a0001c0005t0001g0116a0001c0005t0001g0214a0001c0005t0001g0215others(3): Show | 6 | HG01884.hp1 HG02897.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.5637-53G>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 40/47 | chr7 | 1474413 | ||||||
chr7:1474420
|
C | T | 1 | a0001c0027t0002g0103 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.5637-60G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 40/47 | chr7 | 1474420 | ||||||
chr7:1474471
|
A | AAC | 159 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(156): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.5637-113_5637-112d others(4): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 40/47 | chr7 | 1474471 | ||||||
chr7:1474531
|
C | T | 1 | a0001c0001t0001g0187 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.5637-171G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 40/47 | chr7 | 1474531 | ||||||
chr7:1474573
|
T | A | 2 | a0001c0001t0001g0211a0001c0001t0001g0212 | 2 | HG03831.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.5636+132A>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 40/47 | chr7 | 1474573 | ||||||
chr7:1474660
|
T | G | 3 | a0001c0002t0002g0009a0001c0002t0002g0061a0001c0002t0002g0072 | 6 | HG00423.hp1 HG00558.hp1 NA19007.hp1 others(3): Show |
intron_variant | MODIFIER | c.5636+45A>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 40/47 | chr7 | 1474660 | ||||||
chr7:1474952
|
G | C | 1 | a0001c0001t0004g0174 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.5503-114C>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 39/47 | chr7 | 1474952 | ||||||
chr7:1475013
|
C | T | 1 | a0001c0036t0010g0226 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.5503-175G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 39/47 | chr7 | 1475013 | ||||||
chr7:1475073
|
G | T | 1 | a0001c0002t0002g0069 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.5503-235C>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 39/47 | chr7 | 1475073 | ||||||
chr7:1475345
|
G | A | 1 | a0001c0002t0002g0052 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.5503-507C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 39/47 | chr7 | 1475345 | ||||||
chr7:1475398
|
C | A | 1 | a0001c0002t0002g0080 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.5502+550G>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 39/47 | chr7 | 1475398 | ||||||
chr7:1475433
|
C | T | 1 | a0001c0002t0002g0021 | 2 | HG03017.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.5502+515G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 39/47 | chr7 | 1475433 | ||||||
chr7:1475497
|
A | C | 2 | a0001c0002t0002g0020a0017c0029t0002g0096 | 3 | HG00642.hp2 HG01123.hp2 HG02015.hp1 |
intron_variant | MODIFIER | c.5502+451T>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 39/47 | chr7 | 1475497 | ||||||
chr7:1475539
|
G | A | 3 | a0001c0001t0001g0111a0001c0001t0001g0113a0013c0043t0001g0112 | 3 | NA19009.hp1 NA19081.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.5502+409C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 39/47 | chr7 | 1475539 | ||||||
chr7:1475589
|
C | T | 1 | a0001c0002t0002g0101 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.5502+359G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 39/47 | chr7 | 1475589 | ||||||
chr7:1475595
|
C | T | 2 | a0001c0001t0001g0031a0001c0001t0001g0207 | 3 | HG02559.hp1 HG02622.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.5502+353G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 39/47 | chr7 | 1475595 | ||||||
chr7:1475615
|
C | T | 1 | a0001c0002t0002g0013 | 3 | HG01069.hp1 HG01071.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.5502+333G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 39/47 | chr7 | 1475615 | ||||||
chr7:1475778
|
G | A | 4 | a0001c0018t0003g0108a0001c0019t0003g0109a0002c0007t0003g0027others(1): Show | 5 | HG02280.hp2 HG02723.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.5502+170C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 39/47 | chr7 | 1475778 | ||||||
chr7:1475824
|
C | T | 1 | a0001c0002t0002g0049 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.5502+124G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 39/47 | chr7 | 1475824 | ||||||
chr7:1475898
|
G | A | 1 | a0001c0002t0002g0025 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.5502+50C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 39/47 | chr7 | 1475898 | ||||||
chr7:1475928
|
C | T | 8 | a0001c0002t0002g0004a0001c0002t0002g0010a0001c0002t0002g0055others(5): Show | 16 | HG00140.hp2 HG00639.hp2 HG00673.hp1 others(13): Show |
intron_variant | MODIFIER | c.5502+20G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 39/47 | chr7 | 1475928 | ||||||
chr7:1475929
|
G | A | 3 | a0001c0006t0005g0044a0001c0006t0005g0227a0001c0006t0005g0228 | 4 | HG01243.hp1 HG02572.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.5502+19C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 39/47 | chr7 | 1475929 | ||||||
chr7:1476078
|
G | A | 1 | a0001c0001t0001g0223 | 1 | HG02615.hp1 | splice_region_variant&intron_variant | LOW | c.5379-7C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 38/47 | chr7 | 1476078 | ||||||
chr7:1476084
|
G | C | 1 | a0001c0001t0001g0132 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.5379-13C>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 38/47 | chr7 | 1476084 | ||||||
chr7:1476134
|
G | A | 1 | a0001c0001t0001g0156 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.5379-63C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 38/47 | chr7 | 1476134 | ||||||
chr7:1476482
|
G | A | 1 | a0001c0036t0010g0226 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.5152-27C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 37/47 | chr7 | 1476482 | ||||||
chr7:1476493
|
G | GCCTCTCC others(14): Show |
107 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0014others(104): Show | 138 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(135): Show |
intron_variant | MODIFIER | c.5151+56_5152-39dup others(21): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 37/47 | chr7 | 1476493 | ||||||
chr7:1476493
|
G | GCCTCTCC others(35): Show |
1 | a0001c0001t0001g0224 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.5151+35_5152-39dup others(42): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 37/47 | chr7 | 1476493 | ||||||
chr7:1476538
|
T | C | 1 | a0001c0036t0010g0226 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.5151+32A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 37/47 | chr7 | 1476538 | ||||||
chr7:1476553
|
A | G | 1 | a0001c0034t0002g0045 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.5151+17T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 37/47 | chr7 | 1476553 | ||||||
chr7:1476671
|
A | G | 1 | a0001c0001t0001g0119 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.5064-14T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 36/47 | chr7 | 1476671 | ||||||
chr7:1476725
|
C | A | 1 | a0001c0001t0001g0194 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.5064-68G>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 36/47 | chr7 | 1476725 | ||||||
chr7:1476727
|
G | C | 1 | a0001c0001t0001g0164 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.5063+67C>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 36/47 | chr7 | 1476727 | ||||||
chr7:1477066
|
G | A | 2 | a0001c0026t0002g0104a0001c0027t0002g0103 | 2 | HG01109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.4939-148C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 35/47 | chr7 | 1477066 | ||||||
chr7:1477139
|
G | A | 5 | a0001c0002t0002g0047a0001c0018t0003g0108a0001c0019t0003g0109others(2): Show | 6 | HG02280.hp2 HG02723.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.4939-221C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 35/47 | chr7 | 1477139 | ||||||
chr7:1477227
|
C | A | 1 | a0001c0001t0001g0208 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.4939-309G>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 35/47 | chr7 | 1477227 | ||||||
chr7:1477352
|
G | A | 1 | a0001c0005t0001g0116 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.4938+198C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 35/47 | chr7 | 1477352 | ||||||
chr7:1477401
|
T | A | 1 | a0001c0002t0002g0079 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.4938+149A>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 35/47 | chr7 | 1477401 | ||||||
chr7:1477425
|
G | A | 1 | a0001c0001t0001g0167 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.4938+125C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 35/47 | chr7 | 1477425 | ||||||
chr7:1477465
|
G | A | 1 | a0001c0001t0001g0185 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.4938+85C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 35/47 | chr7 | 1477465 | ||||||
chr7:1477470
|
G | A | 1 | a0001c0026t0002g0104 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.4938+80C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 35/47 | chr7 | 1477470 | ||||||
chr7:1477526
|
G | A | 1 | a0001c0034t0002g0045 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.4938+24C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 35/47 | chr7 | 1477526 | ||||||
chr7:1477700
|
G | C | 3 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135 | 3 | HG02630.hp2 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.4815-27C>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 34/47 | chr7 | 1477700 | ||||||
chr7:1477945
|
G | A | 1 | a0001c0002t0002g0051 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.4631-9C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 33/47 | chr7 | 1477945 | ||||||
chr7:1478030
|
G | T | 6 | a0001c0008t0003g0018a0001c0008t0003g0048a0001c0018t0003g0108others(3): Show | 8 | HG02280.hp2 HG02723.hp1 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.4631-94C>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 33/47 | chr7 | 1478030 | ||||||
chr7:1478033
|
T | A | 1 | a0001c0012t0001g0117 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.4631-97A>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 33/47 | chr7 | 1478033 | ||||||
chr7:1478064
|
A | G | 167 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(164): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.4631-128T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 33/47 | chr7 | 1478064 | ||||||
chr7:1478076
|
G | T | 4 | a0001c0005t0001g0116a0001c0005t0001g0214a0001c0005t0001g0215others(1): Show | 4 | HG01884.hp1 HG02897.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.4631-140C>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 33/47 | chr7 | 1478076 | ||||||
chr7:1478082
|
A | G | 158 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(155): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.4631-146T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 33/47 | chr7 | 1478082 | ||||||
chr7:1478096
|
AGGAGAGT others(12): Show |
A | 2 | a0001c0001t0001g0037a0001c0003t0001g0199 | 3 | HG01070.hp1 HG01243.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.4631-179_4631-161d others(21): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 33/47 | chr7 | 1478096 | ||||||
chr7:1478105
|
C | T | 1 | a0001c0005t0001g0215 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.4631-169G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 33/47 | chr7 | 1478105 | ||||||
chr7:1478115
|
T | C | 2 | a0001c0005t0001g0139a0001c0005t0001g0140 | 2 | HG00280.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.4631-179A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 33/47 | chr7 | 1478115 | ||||||
chr7:1478161
|
T | C | 2 | a0001c0009t0001g0043a0001c0009t0001g0220 | 3 | HG02895.hp1 HG03130.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.4630+205A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 33/47 | chr7 | 1478161 | ||||||
chr7:1478230
|
G | A | 9 | a0001c0008t0003g0018a0001c0008t0003g0048a0001c0018t0003g0108others(6): Show | 11 | HG01109.hp2 HG02280.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.4630+136C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 33/47 | chr7 | 1478230 | ||||||
chr7:1478335
|
G | A | 9 | a0001c0002t0002g0004a0001c0002t0002g0010a0001c0002t0002g0024others(6): Show | 18 | HG00140.hp2 HG00639.hp2 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.4630+31C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 33/47 | chr7 | 1478335 | ||||||
chr7:1478555
|
C | T | 2 | a0001c0005t0001g0139a0001c0005t0001g0140 | 2 | HG00280.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.4490-49G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 32/47 | chr7 | 1478555 | ||||||
chr7:1478700
|
G | A | 144 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(141): Show | 187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.4489+26C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 32/47 | chr7 | 1478700 | ||||||
chr7:1478909
|
G | T | 1 | a0001c0002t0002g0013 | 3 | HG01069.hp1 HG01071.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.4330-24C>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 31/47 | chr7 | 1478909 | ||||||
chr7:1478930
|
C | T | 4 | a0001c0003t0001g0029a0001c0003t0001g0197a0001c0037t0001g0198others(1): Show | 5 | HG02257.hp2 HG02886.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.4330-45G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 31/47 | chr7 | 1478930 | ||||||
chr7:1479054
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.4330-169C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 31/47 | chr7 | 1479054 | ||||||
chr7:1479112
|
C | T | 1 | a0001c0001t0001g0130 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.4330-227G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 31/47 | chr7 | 1479112 | ||||||
chr7:1479233
|
T | C | 158 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(155): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.4329+197A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 31/47 | chr7 | 1479233 | ||||||
chr7:1479247
|
G | C | 1 | a0001c0001t0001g0141 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4329+183C>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 31/47 | chr7 | 1479247 | ||||||
chr7:1479375
|
G | A | 142 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(139): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.4329+55C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 31/47 | chr7 | 1479375 | ||||||
chr7:1479725
|
A | G | 158 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(155): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.4075-41T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 30/47 | chr7 | 1479725 | ||||||
chr7:1479756
|
G | A | 1 | a0001c0001t0004g0173 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.4075-72C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 30/47 | chr7 | 1479756 | ||||||
chr7:1479909
|
G | A | 2 | a0001c0001t0001g0157a0001c0001t0001g0159 | 2 | NA18950.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.4075-225C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 30/47 | chr7 | 1479909 | ||||||
chr7:1479938
|
G | A | 1 | a0014c0024t0002g0067 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.4075-254C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 30/47 | chr7 | 1479938 | ||||||
chr7:1480100
|
A | G | 1 | a0001c0006t0005g0044 | 2 | HG02630.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.4074+217T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 30/47 | chr7 | 1480100 | ||||||
chr7:1480128
|
T | C | 2 | a0001c0001t0001g0111a0001c0001t0001g0113 | 2 | NA19009.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.4074+189A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 30/47 | chr7 | 1480128 | ||||||
chr7:1480191
|
C | T | 6 | a0001c0005t0001g0116a0001c0005t0001g0214a0001c0005t0001g0215others(3): Show | 6 | HG01884.hp1 HG02145.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.4074+126G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 30/47 | chr7 | 1480191 | ||||||
chr7:1480256
|
C | G | 158 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(155): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.4074+61G>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 30/47 | chr7 | 1480256 | ||||||
chr7:1480268
|
G | A | 4 | a0001c0006t0005g0044a0001c0006t0005g0227a0001c0006t0005g0228others(1): Show | 5 | HG01243.hp1 HG02572.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.4074+49C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 30/47 | chr7 | 1480268 | ||||||
chr7:1480310
|
A | T | 158 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(155): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
splice_region_variant&intron_variant | LOW | c.4074+7T>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 30/47 | chr7 | 1480310 | ||||||
chr7:1480527
|
G | A | 14 | a0001c0003t0001g0029a0001c0003t0001g0040a0001c0003t0001g0042others(11): Show | 19 | HG01243.hp1 HG01243.hp2 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.3950-86C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 29/47 | chr7 | 1480527 | ||||||
chr7:1480531
|
G | A | 1 | a0001c0008t0003g0048 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.3950-90C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 29/47 | chr7 | 1480531 | ||||||
chr7:1480636
|
G | A | 4 | a0001c0006t0005g0044a0001c0006t0005g0227a0001c0006t0005g0228others(1): Show | 5 | HG01243.hp1 HG02572.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.3950-195C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 29/47 | chr7 | 1480636 | ||||||
chr7:1480643
|
C | A | 6 | a0001c0005t0001g0116a0001c0005t0001g0214a0001c0005t0001g0215others(3): Show | 6 | HG01884.hp1 HG02145.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.3949+192G>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 29/47 | chr7 | 1480643 | ||||||
chr7:1480707
|
G | T | 1 | a0001c0001t0001g0221 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3949+128C>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 29/47 | chr7 | 1480707 | ||||||
chr7:1480965
|
C | T | 5 | a0001c0018t0003g0108a0001c0019t0003g0109a0001c0020t0003g0110others(2): Show | 6 | HG02280.hp2 HG02723.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.3851-32G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 28/47 | chr7 | 1480965 | ||||||
chr7:1481207
|
G | A | 13 | a0001c0005t0001g0116a0001c0005t0001g0214a0001c0005t0001g0215others(10): Show | 15 | HG01884.hp1 HG02145.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.3850+135C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 28/47 | chr7 | 1481207 | ||||||
chr7:1481315
|
C | G | 6 | a0001c0005t0001g0116a0001c0005t0001g0214a0001c0005t0001g0215others(3): Show | 6 | HG01884.hp1 HG02145.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.3850+27G>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 28/47 | chr7 | 1481315 | ||||||
chr7:1481321
|
C | T | 1 | a0001c0008t0003g0018 | 2 | HG02738.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.3850+21G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 28/47 | chr7 | 1481321 | ||||||
chr7:1481554
|
G | A | 1 | a0001c0005t0001g0216 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3704-66C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 27/47 | chr7 | 1481554 | ||||||
chr7:1481577
|
A | G | 1 | a0001c0035t0001g0143 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3704-89T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 27/47 | chr7 | 1481577 | ||||||
chr7:1481608
|
C | T | 1 | a0001c0036t0010g0226 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3704-120G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 27/47 | chr7 | 1481608 | ||||||
chr7:1481616
|
C | T | 1 | a0001c0001t0001g0153 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.3704-128G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 27/47 | chr7 | 1481616 | ||||||
chr7:1481630
|
AAGACCTG others(101): Show |
A | 7 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0157others(4): Show | 14 | HG00438.hp1 HG01099.hp2 HG02004.hp2 others(11): Show |
intron_variant | MODIFIER | c.3704-250_3704-143d others(2): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 27/47 | chr7 | 1481630 | ||||||
chr7:1481653
|
G | A | 3 | a0001c0006t0005g0044a0001c0006t0005g0227a0001c0006t0005g0228 | 4 | HG01243.hp1 HG02572.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.3704-165C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 27/47 | chr7 | 1481653 | ||||||
chr7:1481670
|
C | A | 15 | a0001c0003t0001g0029a0001c0003t0001g0040a0001c0003t0001g0042others(12): Show | 20 | HG01243.hp1 HG01243.hp2 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.3704-182G>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 27/47 | chr7 | 1481670 | ||||||
chr7:1481695
|
C | A | 3 | a0001c0001t0004g0038a0001c0001t0004g0165a0001c0001t0004g0174 | 4 | HG00558.hp2 HG00597.hp2 HG02071.hp1 others(1): Show |
intron_variant | MODIFIER | c.3704-207G>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 27/47 | chr7 | 1481695 | ||||||
chr7:1481903
|
G | A | 2 | a0001c0026t0002g0104a0001c0027t0002g0103 | 2 | HG01109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.3704-415C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 27/47 | chr7 | 1481903 | ||||||
chr7:1481947
|
C | A | 1 | a0001c0002t0002g0075 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.3704-459G>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 27/47 | chr7 | 1481947 | ||||||
chr7:1481967
|
C | T | 2 | a0001c0001t0001g0034a0001c0001t0001g0218 | 3 | HG02109.hp1 HG02622.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.3704-479G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 27/47 | chr7 | 1481967 | ||||||
chr7:1482086
|
C | T | 6 | a0001c0005t0001g0116a0001c0005t0001g0214a0001c0005t0001g0215others(3): Show | 6 | HG01884.hp1 HG02145.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.3703+460G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 27/47 | chr7 | 1482086 | ||||||
chr7:1482239
|
T | C | 158 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(155): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.3703+307A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 27/47 | chr7 | 1482239 | ||||||
chr7:1482311
|
G | A | 2 | a0001c0001t0001g0017a0001c0001t0001g0187 | 4 | HG01891.hp2 HG02055.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.3703+235C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 27/47 | chr7 | 1482311 | ||||||
chr7:1482319
|
C | G | 1 | a0001c0001t0001g0146 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.3703+227G>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 27/47 | chr7 | 1482319 | ||||||
chr7:1482337
|
C | T | 2 | a0001c0002t0002g0068a0001c0002t0002g0092 | 2 | HG02083.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.3703+209G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 27/47 | chr7 | 1482337 | ||||||
chr7:1482497
|
C | T | 2 | a0001c0026t0002g0104a0001c0027t0002g0103 | 2 | HG01109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.3703+49G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 27/47 | chr7 | 1482497 | ||||||
chr7:1482498
|
G | A | 8 | a0001c0003t0001g0029a0001c0003t0001g0040a0001c0003t0001g0042others(5): Show | 11 | HG01243.hp2 HG01255.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.3703+48C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 27/47 | chr7 | 1482498 | ||||||
chr7:1482521
|
T | C | 151 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(148): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.3703+25A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 27/47 | chr7 | 1482521 | ||||||
chr7:1482539
|
A | G | 184 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(181): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
splice_region_variant&intron_variant | LOW | c.3703+7T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 27/47 | chr7 | 1482539 | ||||||
chr7:1482777
|
A | T | 16 | a0001c0003t0001g0029a0001c0003t0001g0040a0001c0003t0001g0042others(13): Show | 21 | HG01243.hp1 HG01243.hp2 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.3542-70T>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 26/47 | chr7 | 1482777 | ||||||
chr7:1482920
|
A | G | 3 | a0001c0002t0002g0007a0001c0002t0002g0091a0001c0002t0006g0066 | 6 | HG00544.hp2 HG01943.hp1 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.3542-213T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 26/47 | chr7 | 1482920 | ||||||
chr7:1482971
|
A | G | 158 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(155): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.3542-264T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 26/47 | chr7 | 1482971 | ||||||
chr7:1483017
|
T | A | 7 | a0001c0008t0003g0018a0001c0008t0003g0048a0001c0018t0003g0108others(4): Show | 9 | HG02280.hp2 HG02723.hp1 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.3542-310A>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 26/47 | chr7 | 1483017 | ||||||
chr7:1483129
|
T | C | 1 | a0008c0033t0008g0118 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3542-422A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 26/47 | chr7 | 1483129 | ||||||
chr7:1483213
|
G | A | 130 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(127): Show | 169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.3542-506C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 26/47 | chr7 | 1483213 | ||||||
chr7:1483248
|
G | C | 129 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(126): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.3541+494C>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 26/47 | chr7 | 1483248 | ||||||
chr7:1483282
|
C | G | 16 | a0001c0003t0001g0029a0001c0003t0001g0040a0001c0003t0001g0042others(13): Show | 21 | HG01243.hp1 HG01243.hp2 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.3541+460G>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 26/47 | chr7 | 1483282 | ||||||
chr7:1483283
|
G | A | 1 | a0001c0002t0002g0086 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.3541+459C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 26/47 | chr7 | 1483283 | ||||||
chr7:1483326
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.3541+416C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 26/47 | chr7 | 1483326 | ||||||
chr7:1483352
|
C | T | 129 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(126): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.3541+390G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 26/47 | chr7 | 1483352 | ||||||
chr7:1483456
|
G | A | 8 | a0001c0003t0001g0029a0001c0003t0001g0040a0001c0003t0001g0042others(5): Show | 11 | HG01243.hp2 HG01255.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.3541+286C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 26/47 | chr7 | 1483456 | ||||||
chr7:1483587
|
G | C | 3 | a0001c0001t0001g0028a0001c0001t0001g0126a0001c0001t0001g0127 | 4 | HG00140.hp1 HG00280.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.3541+155C>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 26/47 | chr7 | 1483587 | ||||||
chr7:1483602
|
G | T | 1 | a0001c0013t0002g0022 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.3541+140C>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 26/47 | chr7 | 1483602 | ||||||
chr7:1483604
|
G | C | 1 | a0001c0038t0001g0115 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3541+138C>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 26/47 | chr7 | 1483604 | ||||||
chr7:1483626
|
G | A | 1 | a0001c0001t0001g0190 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.3541+116C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 26/47 | chr7 | 1483626 | ||||||
chr7:1483631
|
G | C | 2 | a0001c0001t0001g0129a0001c0041t0001g0128 | 2 | NA19068.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.3541+111C>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 26/47 | chr7 | 1483631 | ||||||
chr7:1483859
|
G | A | 5 | a0001c0018t0003g0108a0001c0019t0003g0109a0001c0020t0003g0110others(2): Show | 6 | HG02280.hp2 HG02723.hp1 HG03098.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.3430-6C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 25/47 | chr7 | 1483859 | ||||||
chr7:1483883
|
A | G | 9 | a0001c0003t0001g0029a0001c0003t0001g0040a0001c0003t0001g0042others(6): Show | 12 | HG01243.hp2 HG01255.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.3430-30T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 25/47 | chr7 | 1483883 | ||||||
chr7:1483923
|
T | C | 159 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(156): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.3430-70A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 25/47 | chr7 | 1483923 | ||||||
chr7:1484192
|
G | A | 2 | a0001c0026t0002g0104a0001c0027t0002g0103 | 2 | HG01109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.3262-22C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 24/47 | chr7 | 1484192 | ||||||
chr7:1484320
|
A | C | 1 | a0001c0005t0001g0116 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.3262-150T>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 24/47 | chr7 | 1484320 | ||||||
chr7:1484320
|
A | G | 157 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(154): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.3262-150T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 24/47 | chr7 | 1484320 | ||||||
chr7:1484384
|
A | G | 8 | a0001c0002t0002g0004a0001c0002t0002g0010a0001c0002t0002g0055others(5): Show | 16 | HG00140.hp2 HG00639.hp2 HG00673.hp1 others(13): Show |
intron_variant | MODIFIER | c.3262-214T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 24/47 | chr7 | 1484384 | ||||||
chr7:1484448
|
T | C | 2 | a0001c0001t0001g0150a0001c0001t0001g0170 | 2 | HG00099.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.3262-278A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 24/47 | chr7 | 1484448 | ||||||
chr7:1484481
|
C | G | 1 | a0001c0002t0002g0073 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.3262-311G>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 24/47 | chr7 | 1484481 | ||||||
chr7:1484593
|
CAT | C | 7 | a0001c0008t0003g0018a0001c0008t0003g0048a0001c0018t0003g0108others(4): Show | 9 | HG02280.hp2 HG02723.hp1 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.3262-425_3262-424d others(4): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 24/47 | chr7 | 1484593 | ||||||
chr7:1484602
|
T | C | 1 | a0001c0036t0010g0226 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3262-432A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 24/47 | chr7 | 1484602 | ||||||
chr7:1484635
|
C | T | 13 | a0001c0003t0001g0029a0001c0003t0001g0040a0001c0003t0001g0042others(10): Show | 18 | HG01243.hp1 HG01243.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.3261+463G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 24/47 | chr7 | 1484635 | ||||||
chr7:1484636
|
G | A | 1 | a0001c0002t0002g0052 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.3261+462C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 24/47 | chr7 | 1484636 | ||||||
chr7:1484659
|
C | T | 7 | a0001c0008t0003g0018a0001c0008t0003g0048a0001c0018t0003g0108others(4): Show | 9 | HG02280.hp2 HG02723.hp1 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.3261+439G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 24/47 | chr7 | 1484659 | ||||||
chr7:1484665
|
G | A | 5 | a0001c0005t0001g0116a0001c0005t0001g0214a0001c0005t0001g0215others(2): Show | 5 | HG01884.hp1 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.3261+433C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 24/47 | chr7 | 1484665 | ||||||
chr7:1484667
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.3261+431C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 24/47 | chr7 | 1484667 | ||||||
chr7:1484717
|
C | T | 3 | a0001c0001t0001g0111a0001c0001t0001g0113a0013c0043t0001g0112 | 3 | NA19009.hp1 NA19081.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.3261+381G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 24/47 | chr7 | 1484717 | ||||||
chr7:1484723
|
C | A | 3 | a0001c0009t0001g0043a0001c0009t0001g0220a0001c0034t0002g0045 | 4 | HG02895.hp1 HG03130.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.3261+375G>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 24/47 | chr7 | 1484723 | ||||||
chr7:1484821
|
C | T | 1 | a0001c0002t0002g0091 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.3261+277G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 24/47 | chr7 | 1484821 | ||||||
chr7:1484847
|
C | T | 5 | a0001c0005t0001g0116a0001c0005t0001g0214a0001c0005t0001g0215others(2): Show | 5 | HG01884.hp1 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.3261+251G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 24/47 | chr7 | 1484847 | ||||||
chr7:1484866
|
T | A | 1 | a0001c0001t0001g0141 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3261+232A>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 24/47 | chr7 | 1484866 | ||||||
chr7:1484943
|
A | ACCCCGTC others(64): Show |
1 | a0001c0001t0001g0159 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.3261+154_3261+155i others(73): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 24/47 | chr7 | 1484943 | ||||||
chr7:1484943
|
A | ACCCCGTC others(28): Show |
15 | a0001c0001t0001g0033a0001c0001t0001g0152a0001c0001t0001g0194others(12): Show | 19 | HG00733.hp2 HG01070.hp2 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.3261+120_3261+154d others(37): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 24/47 | chr7 | 1484943 | ||||||
chr7:1484943
|
A | ACCCCGTC others(63): Show |
118 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(115): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.3261+85_3261+154du others(71): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 24/47 | chr7 | 1484943 | ||||||
chr7:1484943
|
A | ACCCCGTC others(98): Show |
3 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135 | 3 | HG02630.hp2 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.3261+50_3261+154du others(106): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 24/47 | chr7 | 1484943 | ||||||
chr7:1484943
|
A | ACCCCGTC others(64): Show |
1 | a0001c0001t0001g0160 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.3261+154_3261+155i others(73): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 24/47 | chr7 | 1484943 | ||||||
chr7:1484943
|
ACCCCGTC others(28): Show |
A | 3 | a0001c0006t0005g0044a0001c0006t0005g0227a0001c0006t0005g0228 | 4 | HG01243.hp1 HG02572.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.3261+120_3261+154d others(37): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 24/47 | chr7 | 1484943 | ||||||
chr7:1484943
|
ACCCCGTC others(63): Show |
A | 7 | a0001c0005t0001g0116a0001c0005t0001g0214a0001c0005t0001g0215others(4): Show | 8 | HG01884.hp1 HG02738.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.3261+85_3261+154de others(71): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 24/47 | chr7 | 1484943 | ||||||
chr7:1485077
|
T | C | 1 | a0008c0033t0008g0118 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3261+21A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 24/47 | chr7 | 1485077 | ||||||
chr7:1485226
|
G | A | 6 | a0001c0002t0002g0004a0001c0002t0002g0055a0001c0002t0002g0062others(3): Show | 11 | HG00140.hp2 HG00639.hp2 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.3157-24C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 23/47 | chr7 | 1485226 | ||||||
chr7:1485504
|
G | A | 1 | a0001c0001t0001g0175 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2977-35C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 22/47 | chr7 | 1485504 | ||||||
chr7:1485566
|
G | A | 11 | a0001c0003t0001g0029a0001c0003t0001g0040a0001c0003t0001g0042others(8): Show | 16 | HG01243.hp1 HG01243.hp2 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.2977-97C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 22/47 | chr7 | 1485566 | ||||||
chr7:1485606
|
G | A | 1 | a0001c0002t0002g0072 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.2977-137C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 22/47 | chr7 | 1485606 | ||||||
chr7:1485627
|
T | C | 2 | a0001c0026t0002g0104a0001c0027t0002g0103 | 2 | HG01109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2977-158A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 22/47 | chr7 | 1485627 | ||||||
chr7:1485686
|
T | C | 1 | a0001c0001t0001g0144 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2977-217A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 22/47 | chr7 | 1485686 | ||||||
chr7:1485789
|
G | A | 13 | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0166others(10): Show | 17 | HG02109.hp1 HG02280.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.2977-320C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 22/47 | chr7 | 1485789 | ||||||
chr7:1485886
|
C | G | 2 | a0001c0002t0002g0073a0001c0002t0002g0074 | 2 | NA18747.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.2977-417G>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 22/47 | chr7 | 1485886 | ||||||
chr7:1485927
|
T | G | 158 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(155): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.2977-458A>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 22/47 | chr7 | 1485927 | ||||||
chr7:1486125
|
A | G | 158 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(155): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.2976+500T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 22/47 | chr7 | 1486125 | ||||||
chr7:1486133
|
C | T | 127 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(124): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.2976+492G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 22/47 | chr7 | 1486133 | ||||||
chr7:1486172
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2976+453C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 22/47 | chr7 | 1486172 | ||||||
chr7:1486196
|
A | G | 2 | a0001c0026t0002g0104a0001c0027t0002g0103 | 2 | HG01109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2976+429T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 22/47 | chr7 | 1486196 | ||||||
chr7:1486269
|
AT | A | 18 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0168others(15): Show | 20 | HG01884.hp1 HG02145.hp2 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.2976+355delA | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 22/47 | chr7 | 1486269 | ||||||
chr7:1486273
|
T | A | 15 | a0001c0003t0001g0029a0001c0003t0001g0040a0001c0003t0001g0042others(12): Show | 20 | HG00280.hp2 HG01175.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.2976+352A>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 22/47 | chr7 | 1486273 | ||||||
chr7:1486274
|
T | A | 13 | a0001c0005t0001g0116a0001c0005t0001g0214a0001c0005t0001g0215others(10): Show | 15 | HG01884.hp1 HG02145.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.2976+351A>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 22/47 | chr7 | 1486274 | ||||||
chr7:1486333
|
G | A | 1 | a0001c0001t0001g0186 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2976+292C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 22/47 | chr7 | 1486333 | ||||||
chr7:1486434
|
T | C | 2 | a0001c0026t0002g0104a0001c0027t0002g0103 | 2 | HG01109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2976+191A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 22/47 | chr7 | 1486434 | ||||||
chr7:1486447
|
T | C | 1 | a0004c0014t0002g0058 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2976+178A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 22/47 | chr7 | 1486447 | ||||||
chr7:1486545
|
G | A | 142 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(139): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.2976+80C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 22/47 | chr7 | 1486545 | ||||||
chr7:1486591
|
G | A | 1 | a0001c0002t0002g0046 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2976+34C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 22/47 | chr7 | 1486591 | ||||||
chr7:1486599
|
G | A | 1 | a0001c0034t0002g0045 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2976+26C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 22/47 | chr7 | 1486599 | ||||||
chr7:1486820
|
C | T | 63 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0014others(60): Show | 83 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(80): Show |
intron_variant | MODIFIER | c.2827-46G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 21/47 | chr7 | 1486820 | ||||||
chr7:1486821
|
G | A | 1 | a0001c0034t0002g0045 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2827-47C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 21/47 | chr7 | 1486821 | ||||||
chr7:1486838
|
C | T | 2 | a0001c0026t0002g0104a0001c0027t0002g0103 | 2 | HG01109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2827-64G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 21/47 | chr7 | 1486838 | ||||||
chr7:1486883
|
G | A | 1 | a0001c0034t0002g0045 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2826+39C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 21/47 | chr7 | 1486883 | ||||||
chr7:1486897
|
G | A | 1 | a0001c0002t0002g0053 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2826+25C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 21/47 | chr7 | 1486897 | ||||||
chr7:1486898
|
G | T | 11 | a0001c0003t0001g0029a0001c0003t0001g0040a0001c0003t0001g0042others(8): Show | 15 | HG01243.hp2 HG01255.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.2826+24C>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 21/47 | chr7 | 1486898 | ||||||
chr7:1487155
|
G | A | 4 | a0001c0002t0002g0012a0001c0002t0002g0023a0001c0002t0002g0073others(1): Show | 7 | HG00438.hp2 NA18747.hp2 NA18977.hp1 others(4): Show |
intron_variant | MODIFIER | c.2647-54C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 20/47 | chr7 | 1487155 | ||||||
chr7:1487169
|
T | C | 1 | a0001c0005t0001g0216 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2647-68A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 20/47 | chr7 | 1487169 | ||||||
chr7:1487175
|
C | T | 5 | a0001c0005t0001g0116a0001c0005t0001g0214a0001c0005t0001g0215others(2): Show | 5 | HG01884.hp1 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2647-74G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 20/47 | chr7 | 1487175 | ||||||
chr7:1487191
|
G | A | 14 | a0001c0005t0001g0116a0001c0005t0001g0214a0001c0005t0001g0215others(11): Show | 16 | HG01109.hp2 HG01884.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.2647-90C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 20/47 | chr7 | 1487191 | ||||||
chr7:1487210
|
A | G | 1 | a0008c0033t0008g0118 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2647-109T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 20/47 | chr7 | 1487210 | ||||||
chr7:1487267
|
G | T | 6 | a0001c0005t0001g0139a0001c0005t0001g0140a0001c0006t0005g0044others(3): Show | 7 | HG00280.hp2 HG01175.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.2646+53C>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 20/47 | chr7 | 1487267 | ||||||
chr7:1487310
|
C | T | 1 | a0008c0033t0008g0118 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2646+10G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 20/47 | chr7 | 1487310 | ||||||
chr7:1487457
|
C | T | 16 | a0001c0005t0001g0116a0001c0005t0001g0214a0001c0005t0001g0215others(13): Show | 18 | HG01109.hp2 HG01884.hp1 HG02145.hp2 others(15): Show |
splice_region_variant&intron_variant | LOW | c.2517-8G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 19/47 | chr7 | 1487457 | ||||||
chr7:1487486
|
C | A | 6 | a0001c0008t0003g0018a0001c0008t0003g0048a0001c0019t0003g0109others(3): Show | 8 | HG02723.hp1 HG02738.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.2517-37G>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 19/47 | chr7 | 1487486 | ||||||
chr7:1487509
|
CCT | C | 3 | a0001c0006t0005g0044a0001c0006t0005g0227a0001c0006t0005g0228 | 4 | HG01243.hp1 HG02572.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.2517-62_2517-61del others(2): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 19/47 | chr7 | 1487509 | ||||||
chr7:1487534
|
G | A | 1 | a0001c0041t0001g0128 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.2517-85C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 19/47 | chr7 | 1487534 | ||||||
chr7:1487619
|
C | T | 143 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(140): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.2516+141G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 19/47 | chr7 | 1487619 | ||||||
chr7:1487690
|
T | A | 1 | a0001c0031t0001g0123 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2516+70A>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 19/47 | chr7 | 1487690 | ||||||
chr7:1487693
|
C | G | 5 | a0001c0001t0001g0016a0001c0001t0001g0119a0001c0001t0001g0167others(2): Show | 7 | HG00544.hp1 HG00621.hp2 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.2516+67G>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 19/47 | chr7 | 1487693 | ||||||
chr7:1487694
|
C | T | 1 | a0001c0001t0001g0176 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2516+66G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 19/47 | chr7 | 1487694 | ||||||
chr7:1487738
|
C | T | 1 | a0001c0034t0002g0045 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2516+22G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 19/47 | chr7 | 1487738 | ||||||
chr7:1487748
|
T | C | 16 | a0001c0005t0001g0116a0001c0005t0001g0214a0001c0005t0001g0215others(13): Show | 19 | HG01109.hp2 HG01884.hp1 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.2516+12A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 19/47 | chr7 | 1487748 | ||||||
chr7:1487969
|
C | T | 1 | a0001c0001t0004g0173 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2319-12G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 18/47 | chr7 | 1487969 | ||||||
chr7:1488051
|
C | T | 158 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(155): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.2319-94G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 18/47 | chr7 | 1488051 | ||||||
chr7:1488075
|
A | G | 13 | a0001c0005t0001g0116a0001c0005t0001g0214a0001c0005t0001g0215others(10): Show | 15 | HG01884.hp1 HG02145.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.2319-118T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 18/47 | chr7 | 1488075 | ||||||
chr7:1488099
|
G | A | 158 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(155): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.2319-142C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 18/47 | chr7 | 1488099 | ||||||
chr7:1488157
|
G | A | 1 | a0001c0001t0001g0141 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2319-200C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 18/47 | chr7 | 1488157 | ||||||
chr7:1488159
|
G | A | 1 | a0001c0026t0002g0104 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2319-202C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 18/47 | chr7 | 1488159 | ||||||
chr7:1488193
|
C | T | 2 | a0001c0002t0002g0095a0011c0023t0002g0087 | 2 | HG02647.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2319-236G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 18/47 | chr7 | 1488193 | ||||||
chr7:1488408
|
G | A | 1 | a0001c0034t0002g0045 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2319-451C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 18/47 | chr7 | 1488408 | ||||||
chr7:1488506
|
C | T | 2 | a0001c0026t0002g0104a0001c0027t0002g0103 | 2 | HG01109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2319-549G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 18/47 | chr7 | 1488506 | ||||||
chr7:1488611
|
G | A | 1 | a0001c0002t0002g0011 | 3 | HG01167.hp2 HG02258.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2319-654C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 18/47 | chr7 | 1488611 | ||||||
chr7:1488671
|
G | A | 1 | a0001c0034t0002g0045 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2318+673C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 18/47 | chr7 | 1488671 | ||||||
chr7:1488697
|
G | T | 1 | a0001c0011t0001g0210 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2318+647C>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 18/47 | chr7 | 1488697 | ||||||
chr7:1488772
|
G | A | 2 | a0001c0026t0002g0104a0001c0027t0002g0103 | 2 | HG01109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2318+572C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 18/47 | chr7 | 1488772 | ||||||
chr7:1488778
|
C | T | 5 | a0001c0005t0001g0116a0001c0005t0001g0214a0001c0005t0001g0215others(2): Show | 5 | HG01884.hp1 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2318+566G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 18/47 | chr7 | 1488778 | ||||||
chr7:1488816
|
C | A | 1 | a0001c0036t0010g0226 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2318+528G>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 18/47 | chr7 | 1488816 | ||||||
chr7:1488937
|
C | T | 1 | a0001c0038t0001g0115 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2318+407G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 18/47 | chr7 | 1488937 | ||||||
chr7:1489025
|
A | G | 157 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(154): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.2318+319T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 18/47 | chr7 | 1489025 | ||||||
chr7:1489048
|
A | G | 157 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(154): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.2318+296T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 18/47 | chr7 | 1489048 | ||||||
chr7:1489087
|
G | A | 1 | a0001c0002t0002g0024 | 2 | HG01099.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2318+257C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 18/47 | chr7 | 1489087 | ||||||
chr7:1489104
|
G | A | 2 | a0001c0026t0002g0104a0001c0027t0002g0103 | 2 | HG01109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2318+240C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 18/47 | chr7 | 1489104 | ||||||
chr7:1489216
|
G | A | 2 | a0001c0026t0002g0104a0001c0027t0002g0103 | 2 | HG01109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2318+128C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 18/47 | chr7 | 1489216 | ||||||
chr7:1489236
|
G | A | 1 | a0001c0002t0002g0053 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2318+108C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 18/47 | chr7 | 1489236 | ||||||
chr7:1489244
|
T | C | 3 | a0001c0006t0005g0044a0001c0006t0005g0227a0001c0006t0005g0228 | 4 | HG01243.hp1 HG02572.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.2318+100A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 18/47 | chr7 | 1489244 | ||||||
chr7:1489304
|
C | T | 1 | a0001c0005t0001g0215 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2318+40G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 18/47 | chr7 | 1489304 | ||||||
chr7:1489308
|
C | T | 1 | a0001c0008t0003g0048 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2318+36G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 18/47 | chr7 | 1489308 | ||||||
chr7:1489311
|
T | TCCCGGGC others(44): Show |
225 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(222): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.2318+32_2318+33ins others(51): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 18/47 | chr7 | 1489311 | ||||||
chr7:1489311
|
T | TCCCGGGC others(44): Show |
1 | a0001c0001t0001g0177 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2318+32_2318+33ins others(51): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 18/47 | chr7 | 1489311 | ||||||
chr7:1489311
|
T | TCCCGGGC others(44): Show |
2 | a0001c0001t0001g0034a0001c0001t0001g0218 | 3 | HG02109.hp1 HG02622.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2318+32_2318+33ins others(51): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 18/47 | chr7 | 1489311 | ||||||
chr7:1489324
|
G | GAGGGGAC others(44): Show |
1 | a0001c0002t0002g0076 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.2318+19_2318+20ins others(51): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 18/47 | chr7 | 1489324 | ||||||
chr7:1489466
|
G | A | 1 | a0001c0038t0001g0115 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2258-62C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 17/47 | chr7 | 1489466 | ||||||
chr7:1489489
|
T | C | 5 | a0001c0001t0001g0016a0001c0001t0001g0119a0001c0001t0001g0167others(2): Show | 7 | HG00544.hp1 HG00621.hp2 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.2258-85A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 17/47 | chr7 | 1489489 | ||||||
chr7:1489565
|
G | A | 121 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(118): Show | 158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.2257+26C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 17/47 | chr7 | 1489565 | ||||||
chr7:1489703
|
G | A | 1 | a0001c0031t0001g0123 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2166-21C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1489703 | ||||||
chr7:1489788
|
G | A | 1 | a0001c0038t0001g0115 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2166-106C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1489788 | ||||||
chr7:1489791
|
C | A | 157 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(154): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.2166-109G>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1489791 | ||||||
chr7:1489796
|
C | T | 7 | a0001c0003t0001g0029a0001c0003t0001g0040a0001c0003t0001g0042others(4): Show | 10 | HG01243.hp2 HG01255.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.2166-114G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1489796 | ||||||
chr7:1489825
|
A | G | 7 | a0001c0008t0003g0018a0001c0008t0003g0048a0001c0018t0003g0108others(4): Show | 9 | HG02280.hp2 HG02723.hp1 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.2166-143T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1489825 | ||||||
chr7:1489863
|
G | A | 1 | a0001c0027t0002g0103 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2166-181C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1489863 | ||||||
chr7:1489925
|
G | A | 3 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0002t0002g0077 | 3 | HG00621.hp1 HG02027.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.2166-243C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1489925 | ||||||
chr7:1489935
|
A | C | 4 | a0001c0002t0002g0026a0001c0002t0002g0088a0001c0002t0002g0095others(1): Show | 5 | HG01891.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.2166-253T>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1489935 | ||||||
chr7:1489950
|
A | G | 1 | a0001c0001t0001g0200 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2166-268T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1489950 | ||||||
chr7:1490002
|
G | A | 1 | a0008c0033t0008g0118 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2166-320C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1490002 | ||||||
chr7:1490020
|
T | C | 1 | a0010c0044t0001g0183 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2166-338A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1490020 | ||||||
chr7:1490054
|
C | T | 2 | a0001c0026t0002g0104a0001c0027t0002g0103 | 2 | HG01109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2166-372G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1490054 | ||||||
chr7:1490089
|
CAG | C | 157 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(154): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.2166-409_2166-408d others(4): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1490089 | ||||||
chr7:1490125
|
A | G | 157 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(154): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.2166-443T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1490125 | ||||||
chr7:1490224
|
C | A | 141 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(138): Show | 184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.2166-542G>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1490224 | ||||||
chr7:1490256
|
G | C | 2 | a0001c0001t0001g0201a0001c0001t0001g0202 | 2 | HG00621.hp1 HG02027.hp2 |
intron_variant | MODIFIER | c.2166-574C>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1490256 | ||||||
chr7:1490420
|
AC | A | 4 | a0001c0006t0005g0044a0001c0006t0005g0227a0001c0006t0005g0228others(1): Show | 5 | HG01243.hp1 HG02572.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2166-739delG | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1490420 | ||||||
chr7:1490434
|
G | A | 6 | a0001c0005t0001g0116a0001c0005t0001g0214a0001c0005t0001g0215others(3): Show | 6 | HG01884.hp1 HG02145.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.2166-752C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1490434 | ||||||
chr7:1490451
|
G | A | 1 | a0001c0001t0001g0169 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2166-769C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1490451 | ||||||
chr7:1490486
|
G | A | 2 | a0001c0026t0002g0104a0001c0027t0002g0103 | 2 | HG01109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2166-804C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1490486 | ||||||
chr7:1490521
|
G | A | 7 | a0001c0008t0003g0018a0001c0008t0003g0048a0001c0018t0003g0108others(4): Show | 9 | HG02280.hp2 HG02723.hp1 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.2166-839C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1490521 | ||||||
chr7:1490561
|
C | T | 1 | a0001c0001t0001g0203 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2166-879G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1490561 | ||||||
chr7:1490746
|
G | C | 1 | a0001c0004t0001g0149 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2166-1064C>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1490746 | ||||||
chr7:1490800
|
T | C | 157 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(154): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.2166-1118A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1490800 | ||||||
chr7:1490829
|
T | C | 157 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(154): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.2166-1147A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1490829 | ||||||
chr7:1490853
|
A | G | 157 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(154): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.2166-1171T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1490853 | ||||||
chr7:1490858
|
A | G | 157 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(154): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.2166-1176T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1490858 | ||||||
chr7:1490870
|
G | A | 1 | a0001c0001t0001g0170 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2166-1188C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1490870 | ||||||
chr7:1491148
|
C | T | 1 | a0002c0007t0003g0107 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2166-1466G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1491148 | ||||||
chr7:1491153
|
G | C | 1 | a0001c0002t0002g0080 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2166-1471C>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1491153 | ||||||
chr7:1491154
|
C | T | 2 | a0001c0026t0002g0104a0001c0027t0002g0103 | 2 | HG01109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2166-1472G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1491154 | ||||||
chr7:1491158
|
G | A | 7 | a0001c0008t0003g0018a0001c0008t0003g0048a0001c0018t0003g0108others(4): Show | 9 | HG02280.hp2 HG02723.hp1 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.2166-1476C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1491158 | ||||||
chr7:1491315
|
C | T | 3 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135 | 3 | HG02630.hp2 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2166-1633G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1491315 | ||||||
chr7:1491316
|
G | A | 2 | a0001c0048t0001g0192a0010c0044t0001g0183 | 2 | HG02717.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2166-1634C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1491316 | ||||||
chr7:1491398
|
G | C | 2 | a0001c0026t0002g0104a0001c0027t0002g0103 | 2 | HG01109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2165+1612C>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1491398 | ||||||
chr7:1491516
|
A | G | 157 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(154): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.2165+1494T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1491516 | ||||||
chr7:1491624
|
G | A | 157 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(154): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.2165+1386C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1491624 | ||||||
chr7:1491625
|
G | C | 129 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(126): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.2165+1385C>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1491625 | ||||||
chr7:1491769
|
G | A | 1 | a0001c0034t0002g0045 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2165+1241C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1491769 | ||||||
chr7:1491803
|
C | T | 1 | a0001c0034t0002g0045 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2165+1207G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1491803 | ||||||
chr7:1492047
|
C | T | 8 | a0001c0002t0002g0002a0001c0002t0002g0013a0001c0002t0002g0049others(5): Show | 15 | HG01069.hp1 HG01071.hp2 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.2165+963G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1492047 | ||||||
chr7:1492148
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2165+862C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1492148 | ||||||
chr7:1492179
|
C | T | 7 | a0001c0008t0003g0018a0001c0008t0003g0048a0001c0018t0003g0108others(4): Show | 9 | HG02280.hp2 HG02723.hp1 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.2165+831G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1492179 | ||||||
chr7:1492407
|
G | A | 2 | a0001c0026t0002g0104a0001c0027t0002g0103 | 2 | HG01109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2165+603C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1492407 | ||||||
chr7:1492521
|
T | C | 1 | a0008c0033t0008g0118 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2165+489A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1492521 | ||||||
chr7:1492581
|
G | A | 124 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(121): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.2165+429C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1492581 | ||||||
chr7:1492613
|
G | C | 1 | a0001c0036t0010g0226 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2165+397C>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1492613 | ||||||
chr7:1492615
|
G | C | 1 | a0001c0026t0002g0104 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2165+395C>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1492615 | ||||||
chr7:1492624
|
C | CATT | 157 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(154): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.2165+385_2165+386i others(5): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1492624 | ||||||
chr7:1492711
|
C | G | 2 | a0001c0026t0002g0104a0001c0027t0002g0103 | 2 | HG01109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2165+299G>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1492711 | ||||||
chr7:1492734
|
G | A | 9 | a0001c0003t0001g0029a0001c0003t0001g0040a0001c0003t0001g0042others(6): Show | 12 | HG01243.hp2 HG01255.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.2165+276C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1492734 | ||||||
chr7:1492748
|
C | T | 15 | a0001c0003t0001g0029a0001c0003t0001g0040a0001c0003t0001g0042others(12): Show | 19 | HG00280.hp2 HG01175.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.2165+262G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1492748 | ||||||
chr7:1492765
|
G | A | 139 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(136): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.2165+245C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1492765 | ||||||
chr7:1492769
|
T | C | 1 | a0001c0002t0002g0088 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2165+241A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1492769 | ||||||
chr7:1492798
|
T | C | 1 | a0001c0002t0002g0102 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2165+212A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1492798 | ||||||
chr7:1492834
|
C | T | 157 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(154): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.2165+176G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1492834 | ||||||
chr7:1492863
|
C | T | 2 | a0001c0026t0002g0104a0001c0027t0002g0103 | 2 | HG01109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2165+147G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1492863 | ||||||
chr7:1492866
|
GGGCTTAC others(27): Show |
G | 1 | a0001c0001t0001g0171 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2165+110_2165+143d others(36): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1492866 | ||||||
chr7:1492899
|
C | T | 154 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(151): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.2165+111G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1492899 | ||||||
chr7:1492900
|
A | G | 156 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(153): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.2165+110T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1492900 | ||||||
chr7:1492910
|
G | A | 5 | a0001c0005t0001g0116a0001c0005t0001g0214a0001c0005t0001g0215others(2): Show | 5 | HG01884.hp1 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2165+100C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1492910 | ||||||
chr7:1492925
|
G | A | 139 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(136): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.2165+85C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1492925 | ||||||
chr7:1492943
|
C | T | 1 | a0008c0033t0008g0118 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2165+67G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1492943 | ||||||
chr7:1492944
|
G | A | 1 | a0001c0001t0001g0127 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2165+66C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1492944 | ||||||
chr7:1492977
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2165+33G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1492977 | ||||||
chr7:1492995
|
G | A | 156 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(153): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.2165+15C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 16/47 | chr7 | 1492995 | ||||||
chr7:1493217
|
G | A | 7 | a0001c0008t0003g0018a0001c0008t0003g0048a0001c0018t0003g0108others(4): Show | 9 | HG02280.hp2 HG02723.hp1 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.2069-111C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 15/47 | chr7 | 1493217 | ||||||
chr7:1493273
|
G | A | 1 | a0001c0034t0002g0045 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2069-167C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 15/47 | chr7 | 1493273 | ||||||
chr7:1493312
|
G | A | 5 | a0001c0005t0001g0139a0001c0005t0001g0140a0001c0006t0005g0044others(2): Show | 6 | HG00280.hp2 HG01175.hp2 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.2069-206C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 15/47 | chr7 | 1493312 | ||||||
chr7:1493372
|
G | A | 7 | a0001c0008t0003g0018a0001c0008t0003g0048a0001c0018t0003g0108others(4): Show | 9 | HG02280.hp2 HG02723.hp1 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.2069-266C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 15/47 | chr7 | 1493372 | ||||||
chr7:1493398
|
G | A | 9 | a0001c0003t0001g0029a0001c0003t0001g0040a0001c0003t0001g0042others(6): Show | 12 | HG01243.hp2 HG01255.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.2069-292C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 15/47 | chr7 | 1493398 | ||||||
chr7:1493409
|
A | T | 3 | a0001c0006t0005g0044a0001c0006t0005g0227a0001c0006t0005g0228 | 4 | HG01243.hp1 HG02572.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.2069-303T>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 15/47 | chr7 | 1493409 | ||||||
chr7:1493415
|
G | A | 1 | a0001c0001t0001g0135 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2069-309C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 15/47 | chr7 | 1493415 | ||||||
chr7:1493458
|
G | A | 8 | a0001c0003t0001g0029a0001c0003t0001g0040a0001c0003t0001g0042others(5): Show | 11 | HG01243.hp2 HG01255.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.2068+296C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 15/47 | chr7 | 1493458 | ||||||
chr7:1493487
|
G | A | 1 | a0001c0027t0002g0103 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2068+267C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 15/47 | chr7 | 1493487 | ||||||
chr7:1493493
|
T | G | 8 | a0001c0003t0001g0029a0001c0003t0001g0040a0001c0003t0001g0042others(5): Show | 11 | HG01243.hp2 HG01255.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.2068+261A>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 15/47 | chr7 | 1493493 | ||||||
chr7:1493500
|
G | A | 1 | a0008c0033t0008g0118 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2068+254C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 15/47 | chr7 | 1493500 | ||||||
chr7:1493502
|
G | A | 1 | a0008c0033t0008g0118 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2068+252C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 15/47 | chr7 | 1493502 | ||||||
chr7:1493558
|
T | C | 1 | a0001c0036t0010g0226 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2068+196A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 15/47 | chr7 | 1493558 | ||||||
chr7:1493574
|
C | T | 3 | a0001c0001t0001g0032a0001c0001t0001g0150a0001c0001t0001g0206 | 4 | HG02723.hp2 HG02922.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.2068+180G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 15/47 | chr7 | 1493574 | ||||||
chr7:1493591
|
C | CG | 157 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(154): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.2068+162dupC | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 15/47 | chr7 | 1493591 | ||||||
chr7:1493613
|
TC | T | 131 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.2068+140delG | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 15/47 | chr7 | 1493613 | ||||||
chr7:1493657
|
T | C | 2 | a0001c0008t0003g0018a0001c0008t0003g0048 | 3 | HG02738.hp1 HG03492.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.2068+97A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 15/47 | chr7 | 1493657 | ||||||
chr7:1493672
|
G | A | 6 | a0001c0002t0002g0078a0001c0002t0002g0079a0001c0002t0002g0090others(3): Show | 6 | HG02027.hp1 HG02040.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.2068+82C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 15/47 | chr7 | 1493672 | ||||||
chr7:1493706
|
C | T | 7 | a0001c0008t0003g0018a0001c0008t0003g0048a0001c0018t0003g0108others(4): Show | 9 | HG02280.hp2 HG02723.hp1 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.2068+48G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 15/47 | chr7 | 1493706 | ||||||
chr7:1493717
|
G | C | 2 | a0001c0008t0003g0018a0001c0008t0003g0048 | 3 | HG02738.hp1 HG03492.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.2068+37C>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 15/47 | chr7 | 1493717 | ||||||
chr7:1493920
|
T | C | 142 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(139): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.1911-9A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 14/47 | chr7 | 1493920 | ||||||
chr7:1493925
|
G | C | 1 | a0001c0001t0001g0111 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1911-14C>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 14/47 | chr7 | 1493925 | ||||||
chr7:1493930
|
A | G | 156 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(153): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.1911-19T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 14/47 | chr7 | 1493930 | ||||||
chr7:1493930
|
A | T | 1 | a0001c0005t0001g0216 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1911-19T>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 14/47 | chr7 | 1493930 | ||||||
chr7:1493974
|
G | A | 18 | a0001c0001t0001g0006a0001c0001t0001g0037a0001c0001t0001g0121others(15): Show | 26 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(23): Show |
intron_variant | MODIFIER | c.1911-63C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 14/47 | chr7 | 1493974 | ||||||
chr7:1494005
|
C | T | 1 | a0001c0002t0002g0080 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1911-94G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 14/47 | chr7 | 1494005 | ||||||
chr7:1494028
|
G | A | 7 | a0001c0008t0003g0018a0001c0008t0003g0048a0001c0018t0003g0108others(4): Show | 9 | HG02280.hp2 HG02723.hp1 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.1911-117C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 14/47 | chr7 | 1494028 | ||||||
chr7:1494152
|
A | C | 156 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(153): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.1911-241T>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 14/47 | chr7 | 1494152 | ||||||
chr7:1494206
|
A | G | 2 | a0001c0001t0001g0201a0001c0001t0001g0202 | 2 | HG00621.hp1 HG02027.hp2 |
intron_variant | MODIFIER | c.1911-295T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 14/47 | chr7 | 1494206 | ||||||
chr7:1494230
|
C | T | 126 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(123): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.1911-319G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 14/47 | chr7 | 1494230 | ||||||
chr7:1494254
|
G | A | 1 | a0001c0001t0001g0176 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1911-343C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 14/47 | chr7 | 1494254 | ||||||
chr7:1494316
|
C | T | 2 | a0001c0009t0001g0043a0001c0009t0001g0220 | 3 | HG02895.hp1 HG03130.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1911-405G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 14/47 | chr7 | 1494316 | ||||||
chr7:1494317
|
G | A | 1 | a0001c0001t0001g0177 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1911-406C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 14/47 | chr7 | 1494317 | ||||||
chr7:1494328
|
G | A | 149 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(146): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.1911-417C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 14/47 | chr7 | 1494328 | ||||||
chr7:1494374
|
G | A | 1 | a0009c0046t0001g0178 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1910+442C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 14/47 | chr7 | 1494374 | ||||||
chr7:1494397
|
C | A | 2 | a0001c0026t0002g0104a0001c0027t0002g0103 | 2 | HG01109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1910+419G>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 14/47 | chr7 | 1494397 | ||||||
chr7:1494409
|
T | C | 156 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(153): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.1910+407A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 14/47 | chr7 | 1494409 | ||||||
chr7:1494431
|
C | T | 8 | a0001c0003t0001g0029a0001c0003t0001g0040a0001c0003t0001g0042others(5): Show | 11 | HG01243.hp2 HG01255.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.1910+385G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 14/47 | chr7 | 1494431 | ||||||
chr7:1494510
|
C | T | 126 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(123): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.1910+306G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 14/47 | chr7 | 1494510 | ||||||
chr7:1494519
|
T | C | 156 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(153): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.1910+297A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 14/47 | chr7 | 1494519 | ||||||
chr7:1494523
|
G | A | 2 | a0001c0001t0001g0017a0001c0001t0001g0187 | 4 | HG01891.hp2 HG02055.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1910+293C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 14/47 | chr7 | 1494523 | ||||||
chr7:1494597
|
T | C | 1 | a0001c0038t0001g0115 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1910+219A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 14/47 | chr7 | 1494597 | ||||||
chr7:1494620
|
C | T | 1 | a0001c0002t0002g0090 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1910+196G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 14/47 | chr7 | 1494620 | ||||||
chr7:1494622
|
T | A | 1 | a0015c0045t0001g0182 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1910+194A>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 14/47 | chr7 | 1494622 | ||||||
chr7:1494733
|
G | T | 1 | a0001c0041t0001g0128 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1910+83C>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 14/47 | chr7 | 1494733 | ||||||
chr7:1494735
|
C | G | 1 | a0001c0041t0001g0128 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1910+81G>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 14/47 | chr7 | 1494735 | ||||||
chr7:1494738
|
T | C | 1 | a0001c0041t0001g0128 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1910+78A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 14/47 | chr7 | 1494738 | ||||||
chr7:1494789
|
A | G | 157 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(154): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.1910+27T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 14/47 | chr7 | 1494789 | ||||||
chr7:1494950
|
G | A | 1 | a0001c0047t0001g0179 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1833-57C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 13/47 | chr7 | 1494950 | ||||||
chr7:1494957
|
C | A | 124 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(121): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.1833-64G>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 13/47 | chr7 | 1494957 | ||||||
chr7:1495067
|
C | T | 1 | a0001c0002t0002g0064 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1833-174G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 13/47 | chr7 | 1495067 | ||||||
chr7:1495083
|
C | G | 9 | a0001c0003t0001g0029a0001c0003t0001g0040a0001c0003t0001g0042others(6): Show | 12 | HG01243.hp2 HG01255.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1833-190G>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 13/47 | chr7 | 1495083 | ||||||
chr7:1495088
|
C | A | 2 | a0001c0026t0002g0104a0001c0027t0002g0103 | 2 | HG01109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1833-195G>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 13/47 | chr7 | 1495088 | ||||||
chr7:1495099
|
G | T | 1 | a0007c0022t0002g0063 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1833-206C>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 13/47 | chr7 | 1495099 | ||||||
chr7:1495115
|
A | AGTGGCCG others(3): Show |
155 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(152): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.1833-223_1833-222i others(12): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 13/47 | chr7 | 1495115 | ||||||
chr7:1495116
|
G | GTGGCCGA others(3): Show |
2 | a0001c0001t0001g0180a0005c0030t0001g0142 | 2 | NA18950.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.1833-224_1833-223i others(12): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 13/47 | chr7 | 1495116 | ||||||
chr7:1495231
|
C | T | 4 | a0001c0005t0001g0116a0001c0005t0001g0214a0001c0005t0001g0215others(1): Show | 4 | HG01884.hp1 HG02897.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1832+202G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 13/47 | chr7 | 1495231 | ||||||
chr7:1495259
|
A | T | 9 | a0001c0003t0001g0029a0001c0003t0001g0040a0001c0003t0001g0042others(6): Show | 12 | HG01243.hp2 HG01255.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1832+174T>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 13/47 | chr7 | 1495259 | ||||||
chr7:1495321
|
G | T | 1 | a0001c0041t0001g0128 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1832+112C>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 13/47 | chr7 | 1495321 | ||||||
chr7:1495351
|
T | G | 9 | a0001c0002t0002g0004a0001c0002t0002g0010a0001c0002t0002g0024others(6): Show | 18 | HG00140.hp2 HG00639.hp2 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.1832+82A>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 13/47 | chr7 | 1495351 | ||||||
chr7:1495415
|
A | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(152): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.1832+18T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 13/47 | chr7 | 1495415 | ||||||
chr7:1495619
|
G | A | 1 | a0012c0040t0004g0181 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1712-66C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 12/47 | chr7 | 1495619 | ||||||
chr7:1495636
|
C | G | 1 | a0001c0002t0002g0082 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1712-83G>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 12/47 | chr7 | 1495636 | ||||||
chr7:1495761
|
G | A | 7 | a0001c0008t0003g0018a0001c0008t0003g0048a0001c0018t0003g0108others(4): Show | 9 | HG02280.hp2 HG02723.hp1 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.1712-208C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 12/47 | chr7 | 1495761 | ||||||
chr7:1495787
|
A | G | 1 | a0001c0002t0002g0082 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1712-234T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 12/47 | chr7 | 1495787 | ||||||
chr7:1495799
|
C | A | 2 | a0001c0026t0002g0104a0001c0027t0002g0103 | 2 | HG01109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1712-246G>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 12/47 | chr7 | 1495799 | ||||||
chr7:1495952
|
AG | A | 7 | a0001c0008t0003g0018a0001c0008t0003g0048a0001c0018t0003g0108others(4): Show | 9 | HG02280.hp2 HG02723.hp1 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.1711+203delC | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 12/47 | chr7 | 1495952 | ||||||
chr7:1495996
|
C | G | 1 | a0006c0032t0004g0205 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1711+160G>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 12/47 | chr7 | 1495996 | ||||||
chr7:1495996
|
C | T | 153 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(150): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.1711+160G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 12/47 | chr7 | 1495996 | ||||||
chr7:1496031
|
T | C | 1 | a0001c0034t0002g0045 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1711+125A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 12/47 | chr7 | 1496031 | ||||||
chr7:1496116
|
A | G | 3 | a0001c0006t0005g0044a0001c0006t0005g0227a0001c0006t0005g0228 | 4 | HG01243.hp1 HG02572.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1711+40T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 12/47 | chr7 | 1496116 | ||||||
chr7:1496136
|
G | C | 1 | a0001c0002t0002g0082 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1711+20C>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 12/47 | chr7 | 1496136 | ||||||
chr7:1496275
|
A | AGCACGGG others(54): Show |
4 | a0001c0005t0001g0139a0001c0005t0001g0140a0001c0036t0010g0226others(1): Show | 4 | HG00280.hp2 HG01175.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1603-72_1603-12dup others(61): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 11/47 | chr7 | 1496275 | ||||||
chr7:1496275
|
A | AGCATGGG others(54): Show |
1 | a0001c0027t0002g0103 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1603-12_1603-11ins others(61): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 11/47 | chr7 | 1496275 | ||||||
chr7:1496275
|
AGCACGGG others(54): Show |
A | 124 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(121): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.1603-72_1603-12del others(61): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 11/47 | chr7 | 1496275 | ||||||
chr7:1496275
|
AGCACGGG others(115): Show |
A | 2 | a0001c0001t0001g0201a0001c0001t0001g0202 | 2 | HG00621.hp1 HG02027.hp2 |
intron_variant | MODIFIER | c.1603-133_1603-12de others(1): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 11/47 | chr7 | 1496275 | ||||||
chr7:1496279
|
C | T | 1 | a0001c0026t0002g0104 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1603-15G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 11/47 | chr7 | 1496279 | ||||||
chr7:1496330
|
G | GGGCGCGG others(53): Show |
1 | a0001c0026t0002g0104 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1603-126_1603-67du others(61): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 11/47 | chr7 | 1496330 | ||||||
chr7:1496344
|
G | A | 1 | a0001c0002t0002g0083 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1603-80C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 11/47 | chr7 | 1496344 | ||||||
chr7:1496445
|
C | A | 1 | a0015c0045t0001g0182 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1603-181G>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 11/47 | chr7 | 1496445 | ||||||
chr7:1496446
|
C | CCACGTGG others(54): Show |
3 | a0001c0006t0005g0044a0001c0006t0005g0227a0001c0006t0005g0228 | 4 | HG01243.hp1 HG02572.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1603-243_1603-183d others(63): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 11/47 | chr7 | 1496446 | ||||||
chr7:1496449
|
C | A | 5 | a0001c0005t0001g0116a0001c0005t0001g0214a0001c0005t0001g0215others(2): Show | 5 | HG01884.hp1 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1603-185G>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 11/47 | chr7 | 1496449 | ||||||
chr7:1496450
|
G | T | 1 | a0001c0041t0001g0128 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1603-186C>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 11/47 | chr7 | 1496450 | ||||||
chr7:1496700
|
G | A | 21 | a0001c0003t0001g0029a0001c0003t0001g0040a0001c0003t0001g0042others(18): Show | 27 | HG00280.hp2 HG01175.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.1603-436C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 11/47 | chr7 | 1496700 | ||||||
chr7:1496753
|
A | G | 2 | a0001c0026t0002g0104a0001c0027t0002g0103 | 2 | HG01109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1602+385T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 11/47 | chr7 | 1496753 | ||||||
chr7:1496800
|
A | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(152): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.1602+338T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 11/47 | chr7 | 1496800 | ||||||
chr7:1496812
|
A | C | 155 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(152): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.1602+326T>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 11/47 | chr7 | 1496812 | ||||||
chr7:1496930
|
T | C | 132 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(129): Show | 171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.1602+208A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 11/47 | chr7 | 1496930 | ||||||
chr7:1496947
|
G | T | 1 | a0001c0034t0002g0045 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1602+191C>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 11/47 | chr7 | 1496947 | ||||||
chr7:1496987
|
G | A | 17 | a0001c0001t0001g0017a0001c0001t0001g0039a0001c0001t0001g0133others(14): Show | 21 | HG01891.hp2 HG02055.hp2 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.1602+151C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 11/47 | chr7 | 1496987 | ||||||
chr7:1496992
|
A | C | 1 | a0001c0041t0001g0128 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1602+146T>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 11/47 | chr7 | 1496992 | ||||||
chr7:1496993
|
C | A | 1 | a0001c0041t0001g0128 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1602+145G>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 11/47 | chr7 | 1496993 | ||||||
chr7:1496994
|
C | G | 154 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(151): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.1602+144G>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 11/47 | chr7 | 1496994 | ||||||
chr7:1496996
|
C | G | 1 | a0001c0041t0001g0128 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1602+142G>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 11/47 | chr7 | 1496996 | ||||||
chr7:1496997
|
A | C | 1 | a0001c0041t0001g0128 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1602+141T>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 11/47 | chr7 | 1496997 | ||||||
chr7:1497081
|
T | C | 155 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(152): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.1602+57A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 11/47 | chr7 | 1497081 | ||||||
chr7:1497087
|
C | T | 1 | a0001c0002t0002g0062 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1602+51G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 11/47 | chr7 | 1497087 | ||||||
chr7:1497333
|
G | A | 1 | a0001c0001t0001g0188 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1426-19C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 10/47 | chr7 | 1497333 | ||||||
chr7:1497439
|
T | C | 155 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(152): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.1426-125A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 10/47 | chr7 | 1497439 | ||||||
chr7:1497449
|
C | T | 1 | a0001c0002t0002g0019 | 2 | HG02145.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1426-135G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 10/47 | chr7 | 1497449 | ||||||
chr7:1497576
|
G | T | 2 | a0001c0008t0003g0018a0001c0008t0003g0048 | 3 | HG02738.hp1 HG03492.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1426-262C>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 10/47 | chr7 | 1497576 | ||||||
chr7:1497594
|
G | A | 155 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(152): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.1426-280C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 10/47 | chr7 | 1497594 | ||||||
chr7:1497705
|
T | C | 1 | a0001c0001t0001g0189 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1426-391A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 10/47 | chr7 | 1497705 | ||||||
chr7:1497776
|
C | T | 1 | a0001c0021t0002g0089 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1426-462G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 10/47 | chr7 | 1497776 | ||||||
chr7:1497777
|
T | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(152): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.1426-463A>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 10/47 | chr7 | 1497777 | ||||||
chr7:1497781
|
T | C | 155 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(152): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.1426-467A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 10/47 | chr7 | 1497781 | ||||||
chr7:1497789
|
A | G | 15 | a0001c0003t0001g0029a0001c0003t0001g0040a0001c0003t0001g0042others(12): Show | 19 | HG00280.hp2 HG01175.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.1426-475T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 10/47 | chr7 | 1497789 | ||||||
chr7:1497803
|
T | C | 155 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(152): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.1426-489A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 10/47 | chr7 | 1497803 | ||||||
chr7:1497826
|
C | T | 1 | a0001c0001t0001g0111 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1426-512G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 10/47 | chr7 | 1497826 | ||||||
chr7:1497941
|
C | A | 1 | a0001c0002t0002g0084 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1425+471G>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 10/47 | chr7 | 1497941 | ||||||
chr7:1498042
|
G | A | 1 | a0001c0001t0001g0190 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1425+370C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 10/47 | chr7 | 1498042 | ||||||
chr7:1498048
|
C | T | 229 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(226): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.1425+364G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 10/47 | chr7 | 1498048 | ||||||
chr7:1498050
|
C | CA | 155 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(152): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.1425+361dupT | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 10/47 | chr7 | 1498050 | ||||||
chr7:1498055
|
T | A | 155 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(152): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.1425+357A>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 10/47 | chr7 | 1498055 | ||||||
chr7:1498065
|
C | G | 1 | a0001c0001t0001g0137 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1425+347G>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 10/47 | chr7 | 1498065 | ||||||
chr7:1498068
|
C | T | 155 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(152): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.1425+344G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 10/47 | chr7 | 1498068 | ||||||
chr7:1498091
|
G | C | 1 | a0001c0036t0010g0226 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1425+321C>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 10/47 | chr7 | 1498091 | ||||||
chr7:1498250
|
A | G | 1 | a0001c0001t0001g0146 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1425+162T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 10/47 | chr7 | 1498250 | ||||||
chr7:1498287
|
G | A | 2 | a0001c0001t0001g0191a0001c0001t0001g0217 | 2 | HG02132.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.1425+125C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 10/47 | chr7 | 1498287 | ||||||
chr7:1498296
|
G | T | 1 | a0001c0002t0002g0061 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1425+116C>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 10/47 | chr7 | 1498296 | ||||||
chr7:1498302
|
T | C | 2 | a0001c0026t0002g0104a0001c0027t0002g0103 | 2 | HG01109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1425+110A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 10/47 | chr7 | 1498302 | ||||||
chr7:1498385
|
G | A | 2 | a0001c0002t0002g0025a0001c0002t0002g0086 | 3 | HG01167.hp1 HG01169.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.1425+27C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 10/47 | chr7 | 1498385 | ||||||
chr7:1498389
|
A | G | 1 | a0001c0034t0002g0045 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1425+23T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 10/47 | chr7 | 1498389 | ||||||
chr7:1498570
|
TAC | T | 2 | a0001c0001t0001g0031a0001c0001t0001g0207 | 3 | HG02559.hp1 HG02622.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1284-19_1284-18del others(2): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 9/47 | chr7 | 1498570 | ||||||
chr7:1498572
|
C | T | 1 | a0001c0002t0002g0060 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1284-19G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 9/47 | chr7 | 1498572 | ||||||
chr7:1498589
|
ACGCCTGT others(10): Show |
A | 5 | a0001c0018t0003g0108a0001c0019t0003g0109a0001c0020t0003g0110others(2): Show | 6 | HG02280.hp2 HG02723.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1284-53_1284-37del others(17): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 9/47 | chr7 | 1498589 | ||||||
chr7:1498642
|
GCCCACAC others(5): Show |
G | 1 | a0001c0001t0002g0105 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1283+53_1283+64del others(12): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 9/47 | chr7 | 1498642 | ||||||
chr7:1498644
|
C | T | 1 | a0001c0035t0001g0143 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1283+63G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 9/47 | chr7 | 1498644 | ||||||
chr7:1498863
|
G | C | 5 | a0001c0002t0002g0026a0001c0002t0002g0088a0001c0002t0002g0093others(2): Show | 6 | HG01891.hp1 HG02486.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1138-11C>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 8/47 | chr7 | 1498863 | ||||||
chr7:1498896
|
C | G | 1 | a0001c0001t0001g0014 | 3 | HG00438.hp1 HG02015.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.1138-44G>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 8/47 | chr7 | 1498896 | ||||||
chr7:1498903
|
A | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(152): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.1138-51T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 8/47 | chr7 | 1498903 | ||||||
chr7:1498907
|
C | T | 1 | a0001c0001t0001g0144 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1138-55G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 8/47 | chr7 | 1498907 | ||||||
chr7:1498959
|
C | A | 146 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(143): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.1137+16G>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 8/47 | chr7 | 1498959 | ||||||
chr7:1498959
|
C | G | 1 | a0006c0032t0004g0205 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1137+16G>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 8/47 | chr7 | 1498959 | ||||||
chr7:1499181
|
G | A | 1 | a0001c0021t0002g0089 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.951-20C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 7/47 | chr7 | 1499181 | ||||||
chr7:1499208
|
G | A | 1 | a0001c0005t0001g0214 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.950+47C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 7/47 | chr7 | 1499208 | ||||||
chr7:1499212
|
G | GC | 17 | a0001c0001t0001g0113a0001c0001t0001g0194a0001c0001t0001g0195others(14): Show | 18 | HG00280.hp2 HG00544.hp2 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.950+42dupG | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 7/47 | chr7 | 1499212 | ||||||
chr7:1499217
|
C | T | 1 | a0001c0035t0001g0143 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.950+38G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 7/47 | chr7 | 1499217 | ||||||
chr7:1499241
|
A | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(152): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.950+14T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 7/47 | chr7 | 1499241 | ||||||
chr7:1499406
|
AT | A | 5 | a0001c0018t0003g0108a0001c0019t0003g0109a0001c0020t0003g0110others(2): Show | 6 | HG02280.hp2 HG02723.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.845-47delA | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 6/47 | chr7 | 1499406 | ||||||
chr7:1499462
|
G | A | 1 | a0001c0002t0002g0095 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.844+11C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 6/47 | chr7 | 1499462 | ||||||
chr7:1499670
|
G | A | 1 | a0001c0001t0001g0212 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.685-38C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 5/47 | chr7 | 1499670 | ||||||
chr7:1499760
|
G | A | 1 | a0001c0001t0001g0196 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.684+124C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 5/47 | chr7 | 1499760 | ||||||
chr7:1499836
|
A | C | 1 | a0001c0001t0001g0138 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.684+48T>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 5/47 | chr7 | 1499836 | ||||||
chr7:1499843
|
G | C | 1 | a0001c0036t0010g0226 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.684+41C>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 5/47 | chr7 | 1499843 | ||||||
chr7:1499845
|
C | T | 1 | a0001c0036t0010g0226 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.684+39G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 5/47 | chr7 | 1499845 | ||||||
chr7:1500045
|
G | A | 1 | a0008c0033t0008g0118 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.547-24C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 4/47 | chr7 | 1500045 | ||||||
chr7:1500163
|
C | T | 123 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(120): Show | 161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
splice_region_variant&intron_variant | LOW | c.546+7G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 4/47 | chr7 | 1500163 | ||||||
chr7:1500382
|
G | A | 1 | a0001c0002t0002g0097 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.350-16C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1500382 | ||||||
chr7:1500413
|
A | G | 157 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(154): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.350-47T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1500413 | ||||||
chr7:1500463
|
A | G | 3 | a0001c0006t0005g0044a0001c0006t0005g0227a0001c0006t0005g0228 | 4 | HG01243.hp1 HG02572.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.350-97T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1500463 | ||||||
chr7:1500512
|
C | A | 1 | a0001c0001t0001g0200 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.350-146G>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1500512 | ||||||
chr7:1500530
|
C | T | 1 | a0001c0001t0001g0141 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.350-164G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1500530 | ||||||
chr7:1500644
|
T | C | 1 | a0001c0001t0001g0121 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.350-278A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1500644 | ||||||
chr7:1500679
|
T | C | 1 | a0001c0034t0002g0045 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.350-313A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1500679 | ||||||
chr7:1500698
|
G | A | 1 | a0001c0001t0001g0122 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.350-332C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1500698 | ||||||
chr7:1500731
|
C | G | 2 | a0001c0002t0002g0011a0001c0010t0001g0030 | 5 | HG01167.hp2 HG02258.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.350-365G>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1500731 | ||||||
chr7:1500749
|
G | A | 2 | a0001c0001t0001g0201a0001c0001t0001g0202 | 2 | HG00621.hp1 HG02027.hp2 |
intron_variant | MODIFIER | c.350-383C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1500749 | ||||||
chr7:1500814
|
T | G | 9 | a0001c0001t0002g0105a0001c0008t0003g0018a0001c0008t0003g0048others(6): Show | 11 | HG02280.hp2 HG02723.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.350-448A>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1500814 | ||||||
chr7:1500866
|
T | C | 148 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(145): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.350-500A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1500866 | ||||||
chr7:1500869
|
G | A | 3 | a0001c0002t0002g0098a0001c0002t0002g0100a0001c0002t0007g0099 | 3 | HG00735.hp2 HG01109.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.350-503C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1500869 | ||||||
chr7:1500899
|
A | C | 148 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(145): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.350-533T>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1500899 | ||||||
chr7:1500905
|
G | A | 1 | a0001c0001t0001g0203 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.350-539C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1500905 | ||||||
chr7:1500955
|
C | T | 6 | a0001c0005t0001g0139a0001c0005t0001g0140a0001c0006t0005g0044others(3): Show | 7 | HG00280.hp2 HG01175.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.350-589G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1500955 | ||||||
chr7:1500977
|
G | C | 1 | a0001c0002t0002g0101 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.350-611C>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1500977 | ||||||
chr7:1501002
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.350-636G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1501002 | ||||||
chr7:1501209
|
C | T | 1 | a0001c0002t0002g0055 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.350-843G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1501209 | ||||||
chr7:1501227
|
G | A | 1 | a0001c0042t0001g0204 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.350-861C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1501227 | ||||||
chr7:1501284
|
CAA | C | 4 | a0001c0001t0001g0136a0001c0011t0001g0041a0001c0011t0001g0210others(1): Show | 5 | HG00639.hp1 HG01081.hp2 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.350-920_350-919del others(2): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1501284 | ||||||
chr7:1501292
|
AAT | A | 140 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(137): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.350-928_350-927del others(2): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1501292 | ||||||
chr7:1501293
|
AT | A | 3 | a0001c0026t0002g0104a0001c0027t0002g0103a0006c0032t0004g0205 | 3 | HG01109.hp2 HG02056.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.350-928delA | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1501293 | ||||||
chr7:1501294
|
T | A | 1 | a0001c0002t0002g0102 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.350-928A>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1501294 | ||||||
chr7:1501298
|
T | A | 2 | a0001c0001t0001g0206a0001c0001t0001g0207 | 2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.350-932A>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1501298 | ||||||
chr7:1501366
|
T | C | 155 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(152): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.350-1000A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1501366 | ||||||
chr7:1501516
|
A | G | 1 | a0001c0002t0002g0054 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.350-1150T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1501516 | ||||||
chr7:1501555
|
A | G | 1 | a0008c0033t0008g0118 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.350-1189T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1501555 | ||||||
chr7:1501562
|
C | T | 3 | a0001c0001t0001g0111a0001c0001t0001g0113a0013c0043t0001g0112 | 3 | NA19009.hp1 NA19081.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.350-1196G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1501562 | ||||||
chr7:1501621
|
G | A | 1 | a0001c0036t0010g0226 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.350-1255C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1501621 | ||||||
chr7:1501626
|
G | C | 1 | a0001c0002t0002g0046 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.350-1260C>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1501626 | ||||||
chr7:1501640
|
C | T | 3 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135 | 3 | HG02630.hp2 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.349+1261G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1501640 | ||||||
chr7:1501801
|
C | G | 1 | a0001c0001t0001g0132 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.349+1100G>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1501801 | ||||||
chr7:1501811
|
C | G | 1 | a0001c0005t0001g0214 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.349+1090G>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1501811 | ||||||
chr7:1501847
|
C | A | 147 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(144): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.349+1054G>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1501847 | ||||||
chr7:1501852
|
G | A | 1 | a0001c0001t0001g0208 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.349+1049C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1501852 | ||||||
chr7:1501933
|
T | G | 2 | a0001c0001t0001g0129a0001c0041t0001g0128 | 2 | NA19068.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.349+968A>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1501933 | ||||||
chr7:1501993
|
C | A | 7 | a0001c0008t0003g0018a0001c0008t0003g0048a0001c0018t0003g0108others(4): Show | 9 | HG02280.hp2 HG02723.hp1 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.349+908G>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1501993 | ||||||
chr7:1501994
|
C | G | 7 | a0001c0008t0003g0018a0001c0008t0003g0048a0001c0018t0003g0108others(4): Show | 9 | HG02280.hp2 HG02723.hp1 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.349+907G>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1501994 | ||||||
chr7:1502070
|
G | T | 1 | a0001c0001t0001g0131 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.349+831C>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1502070 | ||||||
chr7:1502202
|
C | T | 6 | a0001c0002t0002g0002a0001c0002t0002g0049a0001c0002t0002g0050others(3): Show | 11 | HG01255.hp1 HG01258.hp1 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.349+699G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1502202 | ||||||
chr7:1502244
|
T | C | 1 | a0001c0001t0001g0209 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.349+657A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1502244 | ||||||
chr7:1502362
|
G | A | 6 | a0001c0005t0001g0116a0001c0005t0001g0214a0001c0005t0001g0215others(3): Show | 6 | HG01884.hp1 HG02145.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.349+539C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1502362 | ||||||
chr7:1502413
|
G | A | 2 | a0001c0011t0001g0041a0001c0011t0001g0210 | 3 | HG00639.hp1 HG01081.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.349+488C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1502413 | ||||||
chr7:1502488
|
G | A | 139 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(136): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.349+413C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1502488 | ||||||
chr7:1502489
|
A | G | 139 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(136): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.349+412T>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1502489 | ||||||
chr7:1502492
|
G | A | 1 | a0001c0038t0001g0115 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.349+409C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1502492 | ||||||
chr7:1502591
|
C | T | 7 | a0001c0008t0003g0018a0001c0008t0003g0048a0001c0018t0003g0108others(4): Show | 9 | HG02280.hp2 HG02723.hp1 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.349+310G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1502591 | ||||||
chr7:1502658
|
C | A | 2 | a0001c0009t0001g0043a0001c0009t0001g0220 | 3 | HG02895.hp1 HG03130.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.349+243G>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1502658 | ||||||
chr7:1502691
|
G | A | 1 | a0008c0033t0008g0118 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.349+210C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1502691 | ||||||
chr7:1502773
|
A | C | 7 | a0001c0005t0001g0116a0001c0005t0001g0214a0001c0005t0001g0215others(4): Show | 7 | HG01884.hp1 HG02145.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.349+128T>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1502773 | ||||||
chr7:1502798
|
C | T | 3 | a0001c0001t0001g0130a0001c0009t0001g0043a0001c0009t0001g0220 | 4 | HG02895.hp1 HG03130.hp1 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.349+103G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1502798 | ||||||
chr7:1502830
|
G | A | 3 | a0001c0006t0005g0044a0001c0006t0005g0227a0001c0006t0005g0228 | 4 | HG01243.hp1 HG02572.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.349+71C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1502830 | ||||||
chr7:1502854
|
G | A | 5 | a0001c0001t0001g0028a0001c0001t0001g0126a0001c0001t0001g0127others(2): Show | 6 | HG00140.hp1 HG00280.hp1 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.349+47C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1502854 | ||||||
chr7:1502869
|
G | T | 1 | a0001c0002t0002g0047 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.349+32C>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 3/47 | chr7 | 1502869 | ||||||
chr7:1503279
|
G | A | 5 | a0001c0005t0001g0116a0001c0005t0001g0214a0001c0005t0001g0215others(2): Show | 5 | HG01884.hp1 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.59-88C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 2/47 | chr7 | 1503279 | ||||||
chr7:1503302
|
G | A | 1 | a0001c0003t0001g0042 | 2 | HG02572.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.59-111C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 2/47 | chr7 | 1503302 | ||||||
chr7:1503344
|
C | T | 2 | a0001c0001t0001g0129a0001c0041t0001g0128 | 2 | NA19068.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.59-153G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 2/47 | chr7 | 1503344 | ||||||
chr7:1503563
|
G | T | 1 | a0001c0002t0002g0046 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.58+340C>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 2/47 | chr7 | 1503563 | ||||||
chr7:1503652
|
G | C | 1 | a0001c0027t0002g0103 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.58+251C>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 2/47 | chr7 | 1503652 | ||||||
chr7:1503663
|
T | C | 1 | a0001c0034t0002g0045 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.58+240A>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 2/47 | chr7 | 1503663 | ||||||
chr7:1503756
|
G | C | 1 | a0001c0001t0001g0217 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.58+147C>G | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 2/47 | chr7 | 1503756 | ||||||
chr7:1503799
|
C | T | 3 | a0001c0001t0001g0028a0001c0001t0001g0126a0001c0001t0001g0127 | 4 | HG00140.hp1 HG00280.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+104G>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 2/47 | chr7 | 1503799 | ||||||
chr7:1503840
|
T | TCCCCAAA others(3): Show |
128 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(125): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.58+53_58+62dupGTCT others(6): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 2/47 | chr7 | 1503840 | ||||||
chr7:1503840
|
T | TCCCCAAA others(13): Show |
2 | a0001c0001t0001g0218a0001c0001t0001g0219 | 2 | HG02622.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.58+43_58+62dupGTCT others(16): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 2/47 | chr7 | 1503840 | ||||||
chr7:1503840
|
T | TTCCCAAA others(3): Show |
2 | a0001c0001t0001g0124a0001c0001t0001g0125 | 2 | NA18959.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.58+62_58+63insGTCT others(6): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 2/47 | chr7 | 1503840 | ||||||
chr7:1503840
|
TCCCCAAA others(3): Show |
T | 3 | a0001c0005t0001g0116a0001c0034t0002g0045a0001c0038t0001g0115 | 3 | HG02897.hp1 HG03486.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.58+53_58+62delGTCT others(6): Show |
INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 2/47 | chr7 | 1503840 | ||||||
chr7:1504007
|
G | A | 1 | a0001c0002t0002g0013 | 3 | HG01069.hp1 HG01071.hp2 HG01175.hp1 |
splice_region_variant&intron_variant | LOW | c.-41-6C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 1/47 | chr7 | 1504007 | ||||||
chr7:1504012
|
G | A | 2 | a0001c0009t0001g0043a0001c0009t0001g0220 | 3 | HG02895.hp1 HG03130.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-41-11C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 1/47 | chr7 | 1504012 | ||||||
chr7:1504084
|
G | T | 3 | a0001c0001t0001g0111a0001c0001t0001g0113a0013c0043t0001g0112 | 3 | NA19009.hp1 NA19081.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.-41-83C>A | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 1/47 | chr7 | 1504084 | ||||||
chr7:1504093
|
AC | A | 4 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(1): Show | 4 | HG01496.hp2 HG02055.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.-41-93delG | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 1/47 | chr7 | 1504093 | ||||||
chr7:1504098
|
G | A | 1 | a0001c0001t0001g0225 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-41-97C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 1/47 | chr7 | 1504098 | ||||||
chr7:1504105
|
T | G | 5 | a0001c0018t0003g0108a0001c0019t0003g0109a0001c0020t0003g0110others(2): Show | 6 | HG02280.hp2 HG02723.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.-41-104A>C | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 1/47 | chr7 | 1504105 | ||||||
chr7:1504173
|
G | A | 4 | a0001c0006t0005g0044a0001c0006t0005g0227a0001c0006t0005g0228others(1): Show | 5 | HG01243.hp1 HG02572.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-42+150C>T | INTS1 | ENSG00000164880.16 | transcript | ENST00000404767.8 | protein_coding | 1/47 | chr7 | 1504173 |