geneid | 4086 |
---|---|
ensemblid | ENSG00000170365.10 |
hgncid | 6767 |
symbol | SMAD1 |
name | SMAD family member 1 |
refseq_nuc | NM_005900.3 |
refseq_prot | NP_005891.1 |
ensembl_nuc | ENST00000302085.9 |
ensembl_prot | ENSP00000305769.4 |
mane_status | MANE Select |
chr | chr4 |
start | 145481853 |
end | 145559176 |
strand | + |
ver | v1.2 |
region | chr4:145481853-145559176 |
region5000 | chr4:145476853-145564176 |
regionname0 | SMAD1_chr4_145481853_145559176 |
regionname5000 | SMAD1_chr4_145476853_145564176 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 465 | 307 | 90 | 56 | 111 | 12 | 36 | 77 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
a0002 | 0/0 | 465 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1398 | 301 | 84 | 56 | 111 | 12 | 36 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
c0002 | 0/0 | 1398 | 4 | 4 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
c0003 | 0/0 | 1398 | 2 | 2 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
c0004 | 0/0 | 1398 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 1605 | 68 | 25 | 12 | 17 | 5 | 9 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
t0002 | 1/0 | 1605 | 65 | 0 | 14 | 44 | 3 | 3 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
t0003 | 0/1 | 1608 | 39 | 1 | 13 | 16 | 3 | 5 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
t0004 | 0/0 | 1606 | 34 | 12 | 2 | 13 | 0 | 7 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
t0005 | 0/0 | 1607 | 17 | 7 | 1 | 9 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
t0006 | 0/0 | 1607 | 10 | 0 | 2 | 5 | 1 | 2 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
t0007 | 0/0 | 1607 | 7 | 6 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
t0008 | 0/0 | 1607 | 6 | 4 | 2 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
t0009 | 0/0 | 1606 | 6 | 1 | 0 | 5 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
t0010 | 0/0 | 1606 | 5 | 3 | 2 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
t0011 | 0/0 | 1607 | 5 | 5 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
t0012 | 0/0 | 1607 | 5 | 5 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
t0013 | 0/0 | 1607 | 4 | 0 | 0 | 0 | 0 | 4 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
t0014 | 0/0 | 1604 | 4 | 4 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
t0015 | 0/0 | 1608 | 3 | 3 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
t0016 | 0/0 | 1607 | 3 | 1 | 1 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
t0017 | 0/0 | 1608 | 3 | 3 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
t0018 | 0/0 | 1606 | 2 | 1 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
t0019 | 0/0 | 1608 | 2 | 0 | 0 | 1 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
t0020 | 0/0 | 1606 | 2 | 2 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
t0021 | 0/0 | 1607 | 2 | 2 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
t0022 | 0/0 | 1607 | 2 | 2 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
t0023 | 0/0 | 1608 | 2 | 0 | 2 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
t0024 | 0/0 | 1608 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
t0025 | 0/0 | 1605 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
t0026 | 0/0 | 1606 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
t0027 | 0/0 | 1608 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
t0028 | 0/0 | 1606 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
t0029 | 0/0 | 1606 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
t0030 | 0/0 | 1608 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
t0031 | 0/0 | 1608 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
t0032 | 0/0 | 1607 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
t0033 | 0/0 | 1605 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
t0034 | 0/0 | 1605 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
t0035 | 0/0 | 1608 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0004 | 0/1 | 3 | 0 | 1 | 0 | 1 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0015 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0016 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0017 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0121 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1398 | 301 | 84 | 56 | 111 | 12 | 36 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
a0001c0002 | 0/0 | 1398 | 4 | 4 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
a0001c0003 | 0/0 | 1398 | 2 | 2 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
a0002c0004 | 0/0 | 1398 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3002 | 68 | 25 | 12 | 17 | 5 | 9 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
a0001c0001t0002 | 1/0 | 3002 | 64 | 0 | 14 | 43 | 3 | 3 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
a0001c0001t0003 | 0/1 | 3005 | 39 | 1 | 13 | 16 | 3 | 5 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
a0001c0001t0004 | 0/0 | 3003 | 34 | 12 | 2 | 13 | 0 | 7 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
a0001c0001t0005 | 0/0 | 3004 | 17 | 7 | 1 | 9 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
a0001c0001t0006 | 0/0 | 3004 | 10 | 0 | 2 | 5 | 1 | 2 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
a0001c0001t0007 | 0/0 | 3004 | 7 | 6 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
a0001c0001t0008 | 0/0 | 3004 | 6 | 4 | 2 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
a0001c0001t0009 | 0/0 | 3003 | 6 | 1 | 0 | 5 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
a0001c0001t0010 | 0/0 | 3003 | 5 | 3 | 2 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
a0001c0001t0011 | 0/0 | 3004 | 5 | 5 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
a0001c0001t0013 | 0/0 | 3004 | 4 | 0 | 0 | 0 | 0 | 4 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
a0001c0001t0014 | 0/0 | 3001 | 4 | 4 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
a0001c0001t0015 | 0/0 | 3005 | 3 | 3 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
a0001c0001t0016 | 0/0 | 3004 | 3 | 1 | 1 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
a0001c0001t0017 | 0/0 | 3005 | 3 | 3 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
a0001c0001t0018 | 0/0 | 3003 | 2 | 1 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
a0001c0001t0019 | 0/0 | 3005 | 2 | 0 | 0 | 1 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
a0001c0001t0020 | 0/0 | 3003 | 2 | 2 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
a0001c0001t0021 | 0/0 | 3004 | 2 | 2 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
a0001c0001t0022 | 0/0 | 3004 | 2 | 2 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
a0001c0001t0023 | 0/0 | 3005 | 2 | 0 | 2 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
a0001c0001t0024 | 0/0 | 3005 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
a0001c0001t0025 | 0/0 | 3002 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
a0001c0001t0026 | 0/0 | 3003 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
a0001c0001t0027 | 0/0 | 3005 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
a0001c0001t0028 | 0/0 | 3003 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
a0001c0001t0029 | 0/0 | 3003 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
a0001c0001t0030 | 0/0 | 3005 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
a0001c0001t0031 | 0/0 | 3005 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
a0001c0001t0032 | 0/0 | 3004 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
a0001c0001t0034 | 0/0 | 3002 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
a0001c0001t0035 | 0/0 | 3005 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
a0001c0002t0012 | 0/0 | 3004 | 3 | 3 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
a0001c0002t0033 | 0/0 | 3002 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
a0001c0003t0012 | 0/0 | 3004 | 2 | 2 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
a0002c0004t0002 | 0/0 | 3002 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | copy fasta | chr4 | 145476853 | 145564176 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0002g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0002g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0002g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0002g0121 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0003g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0003g0004 | 0/1 | 3 | 0 | 1 | 0 | 1 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0003g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0003g0015 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0003g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0003g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0003g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0003g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0003g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0003g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0003g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0003g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0003g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0003g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0003g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0004g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0004g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0004g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0004g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0004g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0004g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0004g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0004g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0004g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0004g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0004g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0004g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0004g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0004g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0004g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0004g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0004g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0004g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0004g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0004g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0004g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0004g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0004g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0004g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0004g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0004g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0004g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0004g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0004g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0004g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0004g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0004g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0005g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0005g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0005g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0005g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0005g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0005g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0005g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0005g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0005g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0005g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0005g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0005g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0005g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0005g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0005g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0005g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0005g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0006g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0006g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0006g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0006g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0006g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0006g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0006g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0006g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0006g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0006g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0007g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0007g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0007g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0007g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0007g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0007g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0008g0016 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0008g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0008g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0008g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0008g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0009g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0009g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0009g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0009g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0009g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0009g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0010g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0010g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0010g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0010g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0011g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0011g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0011g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0011g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0011g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0013g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0013g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0013g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0013g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0014g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0014g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0014g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0014g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0015g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0015g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0015g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0016g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0016g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0016g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0017g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0017g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0017g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0018g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0018g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0019g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0019g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0020g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0020g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0021g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0021g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0022g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0022g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0023g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0023g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0024g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0025g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0026g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0027g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0028g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0029g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0030g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0031g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0032g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0034g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0001t0035g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0002t0012g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0002t0012g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0002t0012g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0002t0033g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0003t0012g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0001c0003t0012g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
a0002c0004t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0003 | g0004 | EUR | GBR | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0095 | EUR | GBR | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0265 | EUR | GBR | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0086 | EUR | GBR | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG00408 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | CHS | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | CHS | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | CHS | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG00423 | hp2 | a0001 | c0001 | t0004 | g0109 | EAS | CHS | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG00438 | hp1 | a0001 | c0001 | t0005 | g0044 | EAS | CHS | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG00438 | hp2 | a0001 | c0001 | t0024 | g0212 | EAS | CHS | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | CHS | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0196 | EAS | CHS | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | CHS | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | CHS | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0183 | EAS | CHS | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG00597 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | CHS | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG00609 | hp1 | a0001 | c0001 | t0003 | g0240 | EAS | CHS | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG00609 | hp2 | a0001 | c0001 | t0003 | g0092 | EAS | CHS | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG00621 | hp1 | a0001 | c0001 | t0004 | g0113 | EAS | CHS | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG00621 | hp2 | a0001 | c0001 | t0003 | g0261 | EAS | CHS | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0085 | AMR | PUR | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG00639 | hp2 | a0001 | c0001 | t0003 | g0131 | AMR | PUR | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG00642 | hp1 | a0001 | c0001 | t0003 | g0015 | AMR | PUR | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0280 | EAS | CHS | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | CHS | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0264 | AMR | PUR | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG00735 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG00738 | hp2 | a0001 | c0001 | t0006 | g0218 | AMR | PUR | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG01069 | hp1 | a0001 | c0001 | t0003 | g0129 | AMR | PUR | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0166 | AMR | PUR | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG01070 | hp2 | a0001 | c0001 | t0023 | g0128 | AMR | PUR | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG01071 | hp2 | a0001 | c0001 | t0003 | g0244 | AMR | PUR | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG01081 | hp2 | a0001 | c0001 | t0006 | g0222 | AMR | PUR | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG01099 | hp1 | a0001 | c0001 | t0003 | g0014 | AMR | PUR | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0194 | AMR | PUR | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG01106 | hp1 | a0001 | c0001 | t0003 | g0241 | AMR | PUR | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0063 | AMR | PUR | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG01167 | hp2 | a0001 | c0001 | t0010 | g0132 | AMR | PUR | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG01169 | hp1 | a0001 | c0001 | t0018 | g0281 | AMR | PUR | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG01169 | hp2 | a0001 | c0001 | t0010 | g0251 | AMR | PUR | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG01175 | hp1 | a0001 | c0001 | t0004 | g0108 | AMR | PUR | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG01175 | hp2 | a0001 | c0001 | t0003 | g0258 | AMR | PUR | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG01192 | hp2 | a0001 | c0001 | t0008 | g0262 | AMR | PUR | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG01243 | hp1 | a0001 | c0001 | t0004 | g0152 | AMR | PUR | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG01243 | hp2 | a0001 | c0001 | t0005 | g0022 | AMR | PUR | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0271 | AMR | CLM | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG01255 | hp2 | a0001 | c0001 | t0003 | g0014 | AMR | CLM | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG01257 | hp1 | a0001 | c0001 | t0003 | g0135 | AMR | CLM | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG01261 | hp1 | a0001 | c0001 | t0007 | g0154 | AMR | CLM | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0184 | AMR | CLM | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0181 | AMR | CLM | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG01358 | hp2 | a0001 | c0001 | t0003 | g0137 | AMR | CLM | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG01433 | hp1 | a0001 | c0001 | t0023 | g0242 | AMR | CLM | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | CLM | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG01496 | hp1 | a0001 | c0001 | t0034 | g0191 | AMR | CLM | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG01496 | hp2 | a0001 | c0001 | t0008 | g0016 | AMR | CLM | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0270 | EUR | IBS | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG01516 | hp2 | a0001 | c0001 | t0003 | g0134 | EUR | IBS | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG01517 | hp1 | a0001 | c0001 | t0003 | g0015 | EUR | IBS | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0273 | EUR | IBS | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG01884 | hp1 | a0001 | c0003 | t0012 | g0144 | AFR | ACB | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG01884 | hp2 | a0001 | c0001 | t0005 | g0045 | AFR | ACB | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG01891 | hp2 | a0001 | c0001 | t0008 | g0016 | AFR | ACB | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PEL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG01934 | hp1 | a0001 | c0001 | t0029 | g0140 | AMR | PEL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0227 | AMR | PEL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PEL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0176 | AMR | PEL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG01981 | hp1 | a0001 | c0001 | t0003 | g0256 | AMR | PEL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | PEL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0170 | AMR | PEL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG01993 | hp2 | a0001 | c0001 | t0003 | g0282 | AMR | PEL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | KHV | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | KHV | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG02040 | hp1 | a0001 | c0001 | t0005 | g0026 | EAS | KHV | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | KHV | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG02055 | hp1 | a0001 | c0001 | t0008 | g0263 | AFR | ACB | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG02055 | hp2 | a0001 | c0001 | t0017 | g0164 | AFR | ACB | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | KHV | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG02071 | hp1 | a0001 | c0001 | t0016 | g0091 | EAS | KHV | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0172 | EAS | KHV | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG02132 | hp1 | a0001 | c0001 | t0005 | g0046 | EAS | KHV | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG02132 | hp2 | a0001 | c0001 | t0004 | g0115 | EAS | KHV | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG02135 | hp2 | a0001 | c0001 | t0005 | g0106 | EAS | KHV | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG02145 | hp1 | a0001 | c0002 | t0012 | g0050 | AFR | ACB | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG02145 | hp2 | a0001 | c0001 | t0014 | g0071 | AFR | ACB | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | PEL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG02148 | hp2 | a0001 | c0001 | t0016 | g0257 | AMR | PEL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | CDX | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CDX | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG02257 | hp1 | a0001 | c0001 | t0016 | g0130 | AFR | ACB | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG02257 | hp2 | a0001 | c0002 | t0012 | g0143 | AFR | ACB | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG02258 | hp2 | a0001 | c0001 | t0004 | g0150 | AFR | ACB | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG02280 | hp1 | a0001 | c0001 | t0017 | g0162 | AFR | ACB | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG02280 | hp2 | a0001 | c0001 | t0004 | g0149 | AFR | ACB | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG02293 | hp1 | a0001 | c0001 | t0025 | g0167 | AMR | PEL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG02451 | hp1 | a0001 | c0001 | t0014 | g0066 | AFR | ACB | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | ACB | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG02572 | hp2 | a0001 | c0001 | t0004 | g0079 | AFR | GWD | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG02602 | hp1 | a0001 | c0001 | t0003 | g0247 | SAS | PJL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG02602 | hp2 | a0001 | c0001 | t0004 | g0117 | SAS | PJL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG02615 | hp1 | a0001 | c0001 | t0004 | g0151 | AFR | GWD | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG02615 | hp2 | a0001 | c0001 | t0004 | g0114 | AFR | GWD | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG02630 | hp1 | a0001 | c0001 | t0007 | g0030 | AFR | GWD | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG02630 | hp2 | a0001 | c0001 | t0004 | g0104 | AFR | GWD | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG02647 | hp1 | a0001 | c0001 | t0007 | g0005 | AFR | GWD | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG02647 | hp2 | a0001 | c0001 | t0011 | g0073 | AFR | GWD | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG02717 | hp1 | a0001 | c0001 | t0004 | g0206 | AFR | GWD | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG02717 | hp2 | a0001 | c0002 | t0012 | g0069 | AFR | GWD | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG02723 | hp2 | a0001 | c0001 | t0022 | g0057 | AFR | GWD | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG02735 | hp1 | a0001 | c0001 | t0013 | g0037 | SAS | PJL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG02809 | hp1 | a0001 | c0001 | t0018 | g0252 | AFR | GWD | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG02886 | hp1 | a0001 | c0001 | t0017 | g0163 | AFR | GWD | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG02886 | hp2 | a0001 | c0001 | t0004 | g0207 | AFR | GWD | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG02895 | hp1 | a0001 | c0001 | t0020 | g0153 | AFR | GWD | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG02895 | hp2 | a0001 | c0001 | t0004 | g0231 | AFR | GWD | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG02896 | hp1 | a0001 | c0001 | t0007 | g0005 | AFR | GWD | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG02896 | hp2 | a0001 | c0001 | t0022 | g0217 | AFR | GWD | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG02897 | hp1 | a0001 | c0001 | t0004 | g0232 | AFR | GWD | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG02897 | hp2 | a0001 | c0001 | t0007 | g0031 | AFR | GWD | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | ESN | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG02965 | hp2 | a0001 | c0001 | t0010 | g0013 | AFR | ESN | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG02976 | hp1 | a0001 | c0001 | t0021 | g0027 | AFR | ESN | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG02976 | hp2 | a0001 | c0001 | t0010 | g0123 | AFR | ESN | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG03017 | hp1 | a0001 | c0001 | t0004 | g0007 | SAS | PJL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG03017 | hp2 | a0001 | c0001 | t0013 | g0036 | SAS | PJL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG03041 | hp1 | a0001 | c0001 | t0008 | g0155 | AFR | GWD | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | GWD | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG03098 | hp1 | a0001 | c0001 | t0008 | g0051 | AFR | MSL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | MSL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG03130 | hp1 | a0001 | c0001 | t0011 | g0040 | AFR | ESN | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG03130 | hp2 | a0001 | c0001 | t0005 | g0023 | AFR | ESN | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG03139 | hp2 | a0001 | c0002 | t0033 | g0075 | AFR | ESN | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG03195 | hp1 | a0001 | c0001 | t0004 | g0053 | AFR | ESN | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | ESN | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | MSL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG03209 | hp2 | a0001 | c0001 | t0011 | g0145 | AFR | MSL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | MSL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG03225 | hp2 | a0001 | c0001 | t0014 | g0039 | AFR | MSL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0204 | SAS | PJL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG03453 | hp1 | a0001 | c0001 | t0015 | g0147 | AFR | MSL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG03453 | hp2 | a0001 | c0001 | t0004 | g0080 | AFR | MSL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG03486 | hp1 | a0001 | c0001 | t0007 | g0019 | AFR | MSL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG03486 | hp2 | a0001 | c0001 | t0028 | g0033 | AFR | MSL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG03490 | hp1 | a0001 | c0001 | t0003 | g0243 | SAS | PJL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG03490 | hp2 | a0001 | c0001 | t0013 | g0038 | SAS | PJL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG03491 | hp1 | a0001 | c0001 | t0003 | g0237 | SAS | PJL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG03492 | hp1 | a0001 | c0001 | t0003 | g0245 | SAS | PJL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG03516 | hp1 | a0001 | c0001 | t0005 | g0025 | AFR | ESN | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG03516 | hp2 | a0001 | c0001 | t0014 | g0067 | AFR | ESN | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG03540 | hp1 | a0001 | c0001 | t0007 | g0032 | AFR | GWD | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG03540 | hp2 | a0001 | c0001 | t0020 | g0077 | AFR | GWD | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | MSL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | MSL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG03654 | hp1 | a0001 | c0001 | t0006 | g0220 | SAS | PJL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG03654 | hp2 | a0001 | c0001 | t0004 | g0226 | SAS | PJL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG03669 | hp1 | a0001 | c0001 | t0035 | g0283 | SAS | PJL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0275 | SAS | PJL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG03688 | hp1 | a0001 | c0001 | t0013 | g0068 | SAS | STU | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0186 | SAS | STU | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0272 | SAS | PJL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG03704 | hp2 | a0001 | c0001 | t0004 | g0007 | SAS | PJL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG03831 | hp1 | a0001 | c0001 | t0004 | g0116 | SAS | BEB | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0276 | SAS | BEB | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG03834 | hp1 | a0001 | c0001 | t0026 | g0213 | SAS | BEB | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG03834 | hp2 | a0001 | c0001 | t0004 | g0105 | SAS | BEB | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG03927 | hp1 | a0001 | c0001 | t0027 | g0279 | SAS | BEB | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0180 | SAS | BEB | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG03942 | hp1 | a0001 | c0001 | t0006 | g0223 | SAS | BEB | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG03942 | hp2 | a0001 | c0001 | t0032 | g0112 | SAS | BEB | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG04199 | hp1 | a0001 | c0001 | t0004 | g0111 | SAS | STU | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0278 | SAS | STU | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG04204 | hp1 | a0001 | c0001 | t0019 | g0219 | SAS | STU | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG04204 | hp2 | a0001 | c0001 | t0003 | g0248 | SAS | STU | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | STU | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG04228 | hp2 | a0001 | c0001 | t0031 | g0284 | SAS | STU | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA18522 | hp1 | a0001 | c0001 | t0021 | g0028 | AFR | YRI | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA18522 | hp2 | a0001 | c0001 | t0010 | g0013 | AFR | YRI | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | CHB | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | CHB | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | YRI | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA18906 | hp2 | a0001 | c0001 | t0011 | g0074 | AFR | YRI | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA18942 | hp1 | a0001 | c0001 | t0003 | g0254 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA18944 | hp1 | a0001 | c0001 | t0004 | g0136 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA18945 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA18952 | hp1 | a0001 | c0001 | t0019 | g0221 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA18956 | hp1 | a0001 | c0001 | t0009 | g0236 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA18956 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA18957 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA18964 | hp1 | a0001 | c0001 | t0004 | g0061 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA18964 | hp2 | a0001 | c0001 | t0005 | g0021 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA18965 | hp2 | a0001 | c0001 | t0004 | g0110 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA18967 | hp1 | a0001 | c0001 | t0003 | g0255 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA18967 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA18970 | hp2 | a0001 | c0001 | t0004 | g0060 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA18972 | hp1 | a0001 | c0001 | t0009 | g0234 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA18973 | hp1 | a0001 | c0001 | t0006 | g0120 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA18974 | hp1 | a0001 | c0001 | t0006 | g0225 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA18974 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA18975 | hp2 | a0001 | c0001 | t0006 | g0118 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA18979 | hp2 | a0001 | c0001 | t0005 | g0035 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA18984 | hp2 | a0001 | c0001 | t0003 | g0133 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA18985 | hp1 | a0001 | c0001 | t0004 | g0285 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA18985 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA18988 | hp1 | a0001 | c0001 | t0005 | g0020 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA18988 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA18990 | hp2 | a0001 | c0001 | t0003 | g0260 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA18991 | hp1 | a0001 | c0001 | t0003 | g0253 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA18994 | hp2 | a0001 | c0001 | t0003 | g0246 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA18995 | hp1 | a0001 | c0001 | t0009 | g0233 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA18998 | hp1 | a0001 | c0001 | t0009 | g0003 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA19001 | hp1 | a0001 | c0001 | t0003 | g0124 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA19001 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA19007 | hp2 | a0001 | c0001 | t0006 | g0119 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA19010 | hp1 | a0001 | c0001 | t0009 | g0235 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA19010 | hp2 | a0001 | c0001 | t0005 | g0049 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA19011 | hp2 | a0001 | c0001 | t0004 | g0059 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | LWK | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA19030 | hp2 | a0001 | c0001 | t0009 | g0286 | AFR | LWK | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | LWK | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA19043 | hp2 | a0001 | c0001 | t0030 | g0142 | AFR | LWK | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA19057 | hp1 | a0001 | c0001 | t0003 | g0127 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA19063 | hp2 | a0001 | c0001 | t0003 | g0125 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA19065 | hp2 | a0001 | c0001 | t0006 | g0126 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA19068 | hp1 | a0001 | c0001 | t0003 | g0239 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA19068 | hp2 | a0001 | c0001 | t0004 | g0062 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA19085 | hp1 | a0001 | c0001 | t0004 | g0259 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA19085 | hp2 | a0002 | c0004 | t0002 | g0174 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA19090 | hp1 | a0001 | c0001 | t0005 | g0043 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA19091 | hp2 | a0001 | c0001 | t0003 | g0238 | EAS | JPT | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0017 | EUR | TSI | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA20752 | hp2 | a0001 | c0001 | t0006 | g0224 | EUR | TSI | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0185 | EUR | TSI | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0266 | EUR | TSI | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG02109 | hp2 | a0001 | c0003 | t0012 | g0072 | AFR | ACB | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | ACB | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG02486 | hp2 | a0001 | c0001 | t0005 | g0048 | AFR | ACB | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG02559 | hp1 | a0001 | c0001 | t0011 | g0041 | AFR | ACB | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | ACB | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG03471 | hp1 | a0001 | c0001 | t0015 | g0148 | AFR | MSL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG03471 | hp2 | a0001 | c0001 | t0005 | g0047 | AFR | MSL | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | USA | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
HG06807 | hp2 | a0001 | c0001 | t0005 | g0042 | AFR | USA | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA20300 | hp1 | a0001 | c0001 | t0015 | g0076 | AFR | USA | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA20300 | hp2 | a0001 | c0001 | t0003 | g0250 | AFR | USA | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | LWK | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
NA21309 | hp2 | a0001 | c0001 | t0005 | g0024 | AFR | LWK | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0004 | REF | REF | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0121 | REF | REF | SMAD1_chr4_145476853_145564176 | SMAD1 | chr4 | 145476853 | 145564176 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:145482037
|
C | T | 1 | a0001 | 2 | HG01070.hp2 HG01433.hp1 |
splice_region_variant | LOW | c.-178C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/7 | chr4 | 145482037 | ||||||
chr4:145514438
|
G | A | 1 | a0001 | 7 | HG01261.hp1 HG02630.hp1 HG02647.hp1 others(4): Show |
splice_region_variant | LOW | c.-176G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/7 | chr4 | 145514438 | ||||||
chr4:145553894
|
A | G | 1 | a0002 | 1 | NA19085.hp2 | missense_variant | MODERATE | c.1108A>G | p.Thr370Ala | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 6/7 | 1470/3002 | 1108/1398 | 370/465 | chr4 | 145553894 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:145514998
|
A | C | 2 | a0001c0002a0001c0003 | 6 | HG01884.hp1 HG02109.hp2 HG02145.hp1 others(3): Show |
synonymous_variant | LOW | c.385A>C | p.Arg129Arg | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/7 | 747/3002 | 385/1398 | 129/465 | chr4 | 145514998 | ||
chr4:145542670
|
T | C | 1 | a0001c0003 | 2 | HG01884.hp1 HG02109.hp2 |
synonymous_variant | LOW | c.747T>C | p.Pro249Pro | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/7 | 1109/3002 | 747/1398 | 249/465 | chr4 | 145542670 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:145481985
|
C | G | 1 | a0001c0001t0035 | 1 | HG03669.hp1 | 5_prime_UTR_variant | MODIFIER | c.-230C>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/7 | 32629 | chr4 | 145481985 | |||||
chr4:145481988
|
C | T | 1 | a0001c0001t0034 | 1 | HG01496.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-227C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/7 | chr4 | 145481988 | ||||||
chr4:145482013
|
A | G | 32 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(29): Show | 240 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(237): Show |
5_prime_UTR_variant | MODIFIER | c.-202A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/7 | 32601 | chr4 | 145482013 | |||||
chr4:145514452
|
A | G | 3 | a0001c0002t0012a0001c0002t0033a0001c0003t0012 | 6 | HG01884.hp1 HG02109.hp2 HG02145.hp1 others(3): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-162A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/7 | chr4 | 145514452 | ||||||
chr4:145558079
|
C | CA | 11 | a0001c0001t0003a0001c0001t0010a0001c0001t0013others(8): Show | 61 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*160dupA | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 7/7 | 161 | INFO_REALIGN_3_PRIME | chr4 | 145558079 | ||||
chr4:145558082
|
A | AC | 4 | a0001c0001t0017a0001c0001t0030a0001c0001t0031others(1): Show | 6 | HG02055.hp2 HG02280.hp1 HG02886.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*148_*149insC | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 7/7 | 149 | chr4 | 145558082 | |||||
chr4:145558083
|
A | C | 6 | a0001c0001t0004a0001c0001t0005a0001c0001t0007others(3): Show | 64 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*149A>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 7/7 | 149 | chr4 | 145558083 | |||||
chr4:145558094
|
AC | A | 3 | a0001c0001t0009a0001c0001t0014a0001c0001t0020 | 12 | HG02145.hp2 HG02451.hp1 HG02895.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*161delC | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 7/7 | 161 | chr4 | 145558094 | |||||
chr4:145558095
|
C | A | 14 | a0001c0001t0003a0001c0001t0006a0001c0001t0008others(11): Show | 80 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*161C>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 7/7 | 161 | chr4 | 145558095 | |||||
chr4:145558136
|
T | C | 1 | a0001c0001t0028 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*202T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 7/7 | 202 | chr4 | 145558136 | |||||
chr4:145558245
|
A | G | 3 | a0001c0001t0006a0001c0001t0019a0001c0001t0027 | 13 | HG00738.hp2 HG01081.hp2 HG03654.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*311A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 7/7 | 311 | chr4 | 145558245 | |||||
chr4:145558326
|
T | A | 1 | a0001c0001t0020 | 2 | HG02895.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*392T>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 7/7 | 392 | chr4 | 145558326 | |||||
chr4:145558335
|
G | A | 1 | a0001c0001t0025 | 1 | HG02293.hp1 | 3_prime_UTR_variant | MODIFIER | c.*401G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 7/7 | 401 | chr4 | 145558335 | |||||
chr4:145558515
|
A | G | 1 | a0001c0001t0022 | 2 | HG02723.hp2 HG02896.hp2 |
3_prime_UTR_variant | MODIFIER | c.*581A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 7/7 | 581 | chr4 | 145558515 | |||||
chr4:145558549
|
T | G | 1 | a0001c0001t0017 | 3 | HG02055.hp2 HG02280.hp1 HG02886.hp1 |
3_prime_UTR_variant | MODIFIER | c.*615T>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 7/7 | 615 | chr4 | 145558549 | |||||
chr4:145558681
|
G | T | 1 | a0001c0001t0011 | 5 | HG02559.hp1 HG02647.hp2 HG03130.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*747G>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 7/7 | 747 | chr4 | 145558681 | |||||
chr4:145558684
|
AC | A | 5 | a0001c0001t0004a0001c0001t0013a0001c0001t0026others(2): Show | 41 | HG00423.hp2 HG00621.hp1 HG01175.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*752delC | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 7/7 | 752 | INFO_REALIGN_3_PRIME | chr4 | 145558684 | ||||
chr4:145558697
|
T | C | 1 | a0001c0001t0017 | 3 | HG02055.hp2 HG02280.hp1 HG02886.hp1 |
3_prime_UTR_variant | MODIFIER | c.*763T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 7/7 | 763 | chr4 | 145558697 | |||||
chr4:145558740
|
C | CTT | 27 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(24): Show | 160 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(157): Show |
3_prime_UTR_variant | MODIFIER | c.*806_*807insTT | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 7/7 | 807 | chr4 | 145558740 | |||||
chr4:145558740
|
C | T | 1 | a0001c0001t0018 | 2 | HG01169.hp1 HG02809.hp1 |
3_prime_UTR_variant | MODIFIER | c.*806C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 7/7 | 806 | chr4 | 145558740 | |||||
chr4:145558787
|
T | C | 1 | a0001c0001t0027 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*853T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 7/7 | 853 | chr4 | 145558787 | |||||
chr4:145558959
|
T | C | 4 | a0001c0001t0008a0001c0001t0015a0001c0001t0020others(1): Show | 13 | HG01192.hp2 HG01496.hp2 HG01891.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1025T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 7/7 | 1025 | chr4 | 145558959 | |||||
chr4:145559078
|
A | T | 1 | a0001c0001t0031 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1144A>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 7/7 | 1144 | chr4 | 145559078 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:145482223
|
A | AC | 132 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0146others(129): Show | 146 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.-177+197dupC | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 145482223 | |||||
chr4:145482223
|
A | ACC | 26 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0264others(23): Show | 29 | HG00140.hp1 HG00673.hp1 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.-177+196_-177+197d others(4): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 145482223 | |||||
chr4:145482223
|
AC | A | 34 | a0001c0001t0001g0052a0001c0001t0001g0054a0001c0001t0001g0055others(31): Show | 37 | HG00438.hp1 HG01167.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.-177+197delC | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 145482223 | |||||
chr4:145482223
|
ACC | A | 20 | a0001c0001t0001g0029a0001c0001t0001g0034a0001c0001t0005g0020others(17): Show | 20 | HG01243.hp2 HG02040.hp1 HG02630.hp1 others(17): Show |
intron_variant | MODIFIER | c.-177+196_-177+197d others(4): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 145482223 | |||||
chr4:145482227
|
C | G | 1 | a0001c0001t0009g0286 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-177+189C>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145482227 | ||||||
chr4:145482231
|
C | G | 1 | a0001c0001t0004g0285 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-177+193C>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145482231 | ||||||
chr4:145482377
|
G | T | 6 | a0001c0001t0013g0036a0001c0001t0013g0037a0001c0001t0013g0038others(3): Show | 6 | HG02451.hp1 HG02735.hp1 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.-177+339G>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145482377 | ||||||
chr4:145482389
|
G | T | 1 | a0001c0001t0013g0038 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-177+351G>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145482389 | ||||||
chr4:145482397
|
C | T | 1 | a0001c0001t0031g0284 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-177+359C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145482397 | ||||||
chr4:145482420
|
G | A | 2 | a0001c0001t0014g0066a0001c0001t0014g0067 | 2 | HG02451.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-177+382G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145482420 | ||||||
chr4:145482495
|
C | T | 4 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(1): Show | 4 | HG01081.hp1 HG01928.hp2 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.-177+457C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145482495 | ||||||
chr4:145482496
|
C | T | 54 | a0001c0001t0001g0249a0001c0001t0003g0003a0001c0001t0003g0004others(51): Show | 60 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.-177+458C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145482496 | ||||||
chr4:145482618
|
C | T | 1 | a0001c0001t0002g0012 | 2 | HG01981.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.-177+580C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145482618 | ||||||
chr4:145482693
|
C | G | 1 | a0001c0001t0003g0261 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-177+655C>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145482693 | ||||||
chr4:145482787
|
T | C | 1 | a0001c0001t0030g0142 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-177+749T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145482787 | ||||||
chr4:145482791
|
G | A | 2 | a0001c0002t0012g0069a0001c0002t0012g0143 | 2 | HG02257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-177+753G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145482791 | ||||||
chr4:145482857
|
C | T | 1 | a0001c0001t0002g0012 | 2 | HG01981.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.-177+819C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145482857 | ||||||
chr4:145483109
|
G | C | 1 | a0001c0001t0001g0070 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-177+1071G>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145483109 | ||||||
chr4:145483116
|
C | T | 1 | a0001c0001t0003g0260 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-177+1078C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145483116 | ||||||
chr4:145483206
|
C | T | 1 | a0001c0001t0005g0035 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-177+1168C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145483206 | ||||||
chr4:145483290
|
T | G | 69 | a0001c0001t0001g0009a0001c0001t0001g0029a0001c0001t0001g0052others(66): Show | 72 | HG00438.hp1 HG01192.hp2 HG01243.hp1 others(69): Show |
intron_variant | MODIFIER | c.-177+1252T>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145483290 | ||||||
chr4:145483390
|
C | G | 8 | a0001c0001t0001g0052a0001c0001t0001g0078a0001c0001t0001g0165others(5): Show | 8 | HG02055.hp2 HG02109.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.-177+1352C>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145483390 | ||||||
chr4:145483500
|
A | G | 6 | a0001c0001t0001g0122a0001c0001t0001g0228a0001c0001t0001g0229others(3): Show | 6 | HG01891.hp1 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-177+1462A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145483500 | ||||||
chr4:145483704
|
G | A | 62 | a0001c0001t0001g0029a0001c0001t0001g0052a0001c0001t0001g0078others(59): Show | 64 | HG00438.hp1 HG01192.hp2 HG01243.hp1 others(61): Show |
intron_variant | MODIFIER | c.-177+1666G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145483704 | ||||||
chr4:145483991
|
C | T | 1 | a0001c0001t0003g0137 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-177+1953C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145483991 | ||||||
chr4:145484001
|
T | G | 36 | a0001c0001t0001g0146a0001c0001t0004g0149a0001c0001t0004g0150others(33): Show | 36 | HG00438.hp1 HG01243.hp1 HG01243.hp2 others(33): Show |
intron_variant | MODIFIER | c.-177+1963T>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145484001 | ||||||
chr4:145484017
|
AGTT | A | 2 | a0001c0001t0001g0017a0001c0001t0001g0264 | 3 | HG00735.hp1 HG03239.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-177+1982_-177+198 others(7): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 145484017 | |||||
chr4:145484559
|
G | A | 1 | a0001c0001t0018g0281 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-177+2521G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145484559 | ||||||
chr4:145484641
|
A | G | 1 | a0001c0001t0030g0142 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-177+2603A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145484641 | ||||||
chr4:145484660
|
A | C | 12 | a0001c0001t0001g0052a0001c0001t0001g0078a0001c0001t0001g0158others(9): Show | 12 | HG02055.hp2 HG02109.hp1 HG02135.hp1 others(9): Show |
intron_variant | MODIFIER | c.-177+2622A>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145484660 | ||||||
chr4:145484869
|
T | A | 12 | a0001c0001t0001g0052a0001c0001t0001g0078a0001c0001t0001g0158others(9): Show | 12 | HG02055.hp2 HG02109.hp1 HG02135.hp1 others(9): Show |
intron_variant | MODIFIER | c.-177+2831T>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145484869 | ||||||
chr4:145484998
|
C | T | 1 | a0001c0001t0002g0280 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-177+2960C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145484998 | ||||||
chr4:145485040
|
C | T | 1 | a0001c0001t0002g0227 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-177+3002C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145485040 | ||||||
chr4:145485278
|
G | A | 4 | a0001c0001t0014g0039a0001c0001t0014g0071a0001c0003t0012g0072others(1): Show | 4 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.-177+3240G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145485278 | ||||||
chr4:145485327
|
C | T | 5 | a0001c0001t0008g0016a0001c0001t0008g0051a0001c0001t0008g0155others(2): Show | 6 | HG01192.hp2 HG01496.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.-177+3289C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145485327 | ||||||
chr4:145485419
|
G | A | 1 | a0001c0002t0012g0143 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-177+3381G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145485419 | ||||||
chr4:145485536
|
T | G | 66 | a0001c0001t0001g0029a0001c0001t0001g0052a0001c0001t0001g0078others(63): Show | 68 | HG00438.hp1 HG01192.hp2 HG01243.hp1 others(65): Show |
intron_variant | MODIFIER | c.-177+3498T>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145485536 | ||||||
chr4:145485687
|
G | A | 286 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0017others(283): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.-177+3649G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145485687 | ||||||
chr4:145485741
|
C | G | 17 | a0001c0001t0001g0122a0001c0001t0001g0228a0001c0001t0001g0229others(14): Show | 17 | HG00738.hp2 HG01081.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.-177+3703C>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145485741 | ||||||
chr4:145485793
|
C | CT | 16 | a0001c0001t0005g0020a0001c0001t0005g0021a0001c0001t0005g0022others(13): Show | 16 | HG00438.hp1 HG01243.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.-177+3761dupT | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 145485793 | |||||
chr4:145486246
|
G | A | 4 | a0001c0001t0014g0039a0001c0001t0014g0071a0001c0003t0012g0072others(1): Show | 4 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.-177+4208G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145486246 | ||||||
chr4:145486372
|
A | G | 66 | a0001c0001t0001g0029a0001c0001t0001g0052a0001c0001t0001g0078others(63): Show | 68 | HG00438.hp1 HG01192.hp2 HG01243.hp1 others(65): Show |
intron_variant | MODIFIER | c.-177+4334A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145486372 | ||||||
chr4:145486528
|
C | CT | 66 | a0001c0001t0001g0029a0001c0001t0001g0052a0001c0001t0001g0078others(63): Show | 68 | HG00438.hp1 HG01192.hp2 HG01243.hp1 others(65): Show |
intron_variant | MODIFIER | c.-177+4490_-177+449 others(5): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145486528 | ||||||
chr4:145486720
|
C | T | 66 | a0001c0001t0001g0029a0001c0001t0001g0052a0001c0001t0001g0078others(63): Show | 68 | HG00438.hp1 HG01192.hp2 HG01243.hp1 others(65): Show |
intron_variant | MODIFIER | c.-177+4682C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145486720 | ||||||
chr4:145486912
|
G | A | 2 | a0001c0001t0021g0027a0001c0001t0021g0028 | 2 | HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-177+4874G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145486912 | ||||||
chr4:145486978
|
T | G | 5 | a0001c0001t0011g0040a0001c0001t0011g0041a0001c0001t0011g0073others(2): Show | 5 | HG02559.hp1 HG02647.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-177+4940T>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145486978 | ||||||
chr4:145487140
|
G | A | 1 | a0001c0001t0001g0265 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-177+5102G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145487140 | ||||||
chr4:145487183
|
A | G | 4 | a0001c0001t0014g0039a0001c0001t0014g0071a0001c0003t0012g0072others(1): Show | 4 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.-177+5145A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145487183 | ||||||
chr4:145487294
|
A | G | 35 | a0001c0001t0001g0029a0001c0001t0001g0146a0001c0001t0004g0149others(32): Show | 36 | HG00438.hp1 HG01243.hp1 HG01243.hp2 others(33): Show |
intron_variant | MODIFIER | c.-177+5256A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145487294 | ||||||
chr4:145487358
|
G | T | 2 | a0001c0001t0021g0027a0001c0001t0021g0028 | 2 | HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-177+5320G>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145487358 | ||||||
chr4:145487372
|
T | C | 7 | a0001c0001t0001g0029a0001c0001t0007g0005a0001c0001t0007g0030others(4): Show | 8 | HG01261.hp1 HG02630.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.-177+5334T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145487372 | ||||||
chr4:145487786
|
G | A | 4 | a0001c0001t0005g0020a0001c0001t0005g0021a0001c0001t0005g0043others(1): Show | 4 | HG00438.hp1 NA18964.hp2 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.-177+5748G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145487786 | ||||||
chr4:145487805
|
C | T | 4 | a0001c0001t0014g0039a0001c0001t0014g0071a0001c0003t0012g0072others(1): Show | 4 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.-177+5767C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145487805 | ||||||
chr4:145487828
|
G | A | 1 | a0001c0001t0003g0260 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-177+5790G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145487828 | ||||||
chr4:145487881
|
AG | A | 62 | a0001c0001t0001g0029a0001c0001t0001g0052a0001c0001t0001g0078others(59): Show | 64 | HG00438.hp1 HG01192.hp2 HG01243.hp1 others(61): Show |
intron_variant | MODIFIER | c.-177+5844delG | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145487881 | ||||||
chr4:145488079
|
T | C | 62 | a0001c0001t0001g0029a0001c0001t0001g0052a0001c0001t0001g0078others(59): Show | 64 | HG00438.hp1 HG01192.hp2 HG01243.hp1 others(61): Show |
intron_variant | MODIFIER | c.-177+6041T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145488079 | ||||||
chr4:145488120
|
CT | C | 14 | a0001c0001t0004g0053a0001c0001t0004g0079a0001c0001t0004g0080others(11): Show | 14 | HG00738.hp2 HG01081.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.-177+6094delT | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 145488120 | |||||
chr4:145488313
|
C | G | 10 | a0001c0001t0011g0040a0001c0001t0011g0041a0001c0001t0011g0073others(7): Show | 10 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.-177+6275C>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145488313 | ||||||
chr4:145488400
|
A | T | 52 | a0001c0001t0001g0029a0001c0001t0001g0052a0001c0001t0001g0078others(49): Show | 54 | HG00438.hp1 HG01192.hp2 HG01243.hp1 others(51): Show |
intron_variant | MODIFIER | c.-177+6362A>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145488400 | ||||||
chr4:145488476
|
T | TTG | 69 | a0001c0001t0001g0034a0001c0001t0001g0107a0001c0001t0001g0138others(66): Show | 74 | HG00099.hp1 HG00423.hp2 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.-177+6465_-177+646 others(6): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 145488476 | |||||
chr4:145488476
|
T | TTGTG | 25 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0122others(22): Show | 25 | HG01081.hp2 HG01167.hp1 HG01175.hp2 others(22): Show |
intron_variant | MODIFIER | c.-177+6463_-177+646 others(8): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 145488476 | |||||
chr4:145488476
|
TTGTGTGT others(3): Show |
T | 1 | a0001c0002t0012g0050 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-177+6457_-177+646 others(14): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 145488476 | |||||
chr4:145488476
|
TTGTGTGT others(5): Show |
T | 61 | a0001c0001t0001g0029a0001c0001t0001g0052a0001c0001t0001g0078others(58): Show | 63 | HG00438.hp1 HG01192.hp2 HG01243.hp1 others(60): Show |
intron_variant | MODIFIER | c.-177+6455_-177+646 others(16): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 145488476 | |||||
chr4:145488556
|
CT | C | 62 | a0001c0001t0001g0029a0001c0001t0001g0052a0001c0001t0001g0078others(59): Show | 64 | HG00438.hp1 HG01192.hp2 HG01243.hp1 others(61): Show |
intron_variant | MODIFIER | c.-177+6526delT | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 145488556 | |||||
chr4:145488629
|
G | A | 10 | a0001c0001t0011g0040a0001c0001t0011g0041a0001c0001t0011g0073others(7): Show | 10 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.-177+6591G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145488629 | ||||||
chr4:145488697
|
G | A | 8 | a0001c0001t0001g0052a0001c0001t0001g0078a0001c0001t0001g0165others(5): Show | 8 | HG02055.hp2 HG02109.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.-177+6659G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145488697 | ||||||
chr4:145488812
|
T | C | 62 | a0001c0001t0001g0029a0001c0001t0001g0052a0001c0001t0001g0078others(59): Show | 64 | HG00438.hp1 HG01192.hp2 HG01243.hp1 others(61): Show |
intron_variant | MODIFIER | c.-177+6774T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145488812 | ||||||
chr4:145488830
|
C | T | 17 | a0001c0001t0003g0134a0001c0001t0003g0256a0001c0001t0005g0020others(14): Show | 17 | HG00438.hp1 HG01243.hp2 HG01516.hp2 others(14): Show |
intron_variant | MODIFIER | c.-177+6792C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145488830 | ||||||
chr4:145489227
|
T | C | 1 | a0001c0001t0023g0128 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-177+7189T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145489227 | ||||||
chr4:145489295
|
G | T | 1 | a0001c0001t0003g0240 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-177+7257G>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145489295 | ||||||
chr4:145489364
|
G | C | 1 | a0001c0001t0004g0105 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-177+7326G>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145489364 | ||||||
chr4:145489393
|
G | A | 58 | a0001c0001t0001g0029a0001c0001t0001g0146a0001c0001t0004g0149others(55): Show | 60 | HG00438.hp1 HG01192.hp2 HG01243.hp1 others(57): Show |
intron_variant | MODIFIER | c.-177+7355G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145489393 | ||||||
chr4:145489478
|
TAAATA | T | 57 | a0001c0001t0001g0029a0001c0001t0001g0146a0001c0001t0004g0149others(54): Show | 59 | HG00438.hp1 HG01192.hp2 HG01243.hp2 others(56): Show |
intron_variant | MODIFIER | c.-177+7449_-177+745 others(9): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 145489478 | |||||
chr4:145489525
|
T | C | 3 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0003g0240 | 3 | HG00609.hp1 HG02135.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.-177+7487T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145489525 | ||||||
chr4:145489848
|
G | A | 59 | a0001c0001t0001g0029a0001c0001t0001g0146a0001c0001t0004g0149others(56): Show | 61 | HG00438.hp1 HG01192.hp2 HG01243.hp1 others(58): Show |
intron_variant | MODIFIER | c.-177+7810G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145489848 | ||||||
chr4:145490038
|
A | T | 98 | a0001c0001t0001g0052a0001c0001t0001g0078a0001c0001t0001g0122others(95): Show | 106 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.-177+8000A>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145490038 | ||||||
chr4:145490039
|
A | C | 98 | a0001c0001t0001g0052a0001c0001t0001g0078a0001c0001t0001g0122others(95): Show | 106 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.-177+8001A>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145490039 | ||||||
chr4:145490056
|
A | C | 2 | a0001c0003t0012g0072a0001c0003t0012g0144 | 2 | HG01884.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.-177+8018A>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145490056 | ||||||
chr4:145490068
|
G | A | 3 | a0001c0001t0002g0166a0001c0001t0002g0227a0001c0001t0025g0167 | 3 | HG01069.hp2 HG01934.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.-177+8030G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145490068 | ||||||
chr4:145490231
|
CA | C | 43 | a0001c0001t0001g0052a0001c0001t0001g0078a0001c0001t0001g0122others(40): Show | 45 | HG00423.hp2 HG00621.hp1 HG01081.hp1 others(42): Show |
intron_variant | MODIFIER | c.-177+8196delA | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 145490231 | |||||
chr4:145490377
|
G | A | 32 | a0001c0001t0001g0029a0001c0001t0001g0146a0001c0001t0004g0149others(29): Show | 33 | HG00438.hp1 HG01243.hp1 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.-177+8339G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145490377 | ||||||
chr4:145490418
|
G | A | 60 | a0001c0001t0001g0029a0001c0001t0001g0078a0001c0001t0001g0146others(57): Show | 62 | HG00438.hp1 HG01192.hp2 HG01243.hp1 others(59): Show |
intron_variant | MODIFIER | c.-177+8380G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145490418 | ||||||
chr4:145490584
|
A | G | 1 | a0001c0001t0001g0141 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-177+8546A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145490584 | ||||||
chr4:145490630
|
C | G | 1 | a0001c0001t0001g0070 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-177+8592C>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145490630 | ||||||
chr4:145490686
|
A | T | 1 | a0001c0001t0002g0211 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-177+8648A>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145490686 | ||||||
chr4:145491046
|
G | T | 2 | a0001c0003t0012g0072a0001c0003t0012g0144 | 2 | HG01884.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.-177+9008G>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145491046 | ||||||
chr4:145491130
|
A | T | 2 | a0001c0001t0011g0074a0001c0001t0011g0145 | 2 | HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-177+9092A>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145491130 | ||||||
chr4:145491228
|
T | C | 1 | a0001c0001t0005g0022 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-177+9190T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145491228 | ||||||
chr4:145491258
|
A | C | 3 | a0001c0002t0012g0050a0001c0002t0012g0069a0001c0002t0012g0143 | 3 | HG02145.hp1 HG02257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-177+9220A>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145491258 | ||||||
chr4:145491531
|
C | T | 1 | a0001c0001t0004g0080 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-177+9493C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145491531 | ||||||
chr4:145491629
|
A | G | 5 | a0001c0001t0008g0016a0001c0001t0008g0051a0001c0001t0008g0155others(2): Show | 6 | HG01192.hp2 HG01496.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.-177+9591A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145491629 | ||||||
chr4:145491716
|
T | C | 1 | a0001c0001t0009g0286 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-177+9678T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145491716 | ||||||
chr4:145491786
|
C | T | 2 | a0001c0001t0014g0039a0001c0001t0014g0071 | 2 | HG02145.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-177+9748C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145491786 | ||||||
chr4:145491810
|
C | T | 1 | a0001c0002t0033g0075 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-177+9772C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145491810 | ||||||
chr4:145491829
|
A | G | 1 | a0001c0001t0002g0277 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-177+9791A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145491829 | ||||||
chr4:145491938
|
A | G | 3 | a0001c0002t0012g0050a0001c0002t0012g0069a0001c0002t0012g0143 | 3 | HG02145.hp1 HG02257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-177+9900A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145491938 | ||||||
chr4:145491950
|
G | A | 1 | a0001c0001t0004g0108 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-177+9912G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145491950 | ||||||
chr4:145492012
|
TA | T | 10 | a0001c0001t0011g0040a0001c0001t0011g0041a0001c0001t0011g0073others(7): Show | 10 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.-177+9982delA | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 145492012 | |||||
chr4:145492192
|
C | T | 4 | a0001c0001t0003g0133a0001c0001t0003g0253a0001c0001t0003g0254others(1): Show | 4 | NA18942.hp1 NA18967.hp1 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.-177+10154C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145492192 | ||||||
chr4:145492399
|
C | T | 10 | a0001c0001t0011g0040a0001c0001t0011g0041a0001c0001t0011g0073others(7): Show | 10 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.-177+10361C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145492399 | ||||||
chr4:145492516
|
G | T | 5 | a0001c0001t0008g0016a0001c0001t0008g0051a0001c0001t0008g0155others(2): Show | 6 | HG01192.hp2 HG01496.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.-177+10478G>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145492516 | ||||||
chr4:145492523
|
G | A | 1 | a0001c0001t0007g0019 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-177+10485G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145492523 | ||||||
chr4:145492666
|
C | G | 1 | a0001c0001t0030g0142 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-177+10628C>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145492666 | ||||||
chr4:145492763
|
T | A | 55 | a0001c0001t0001g0029a0001c0001t0001g0146a0001c0001t0005g0020others(52): Show | 57 | HG00438.hp1 HG01192.hp2 HG01243.hp2 others(54): Show |
intron_variant | MODIFIER | c.-177+10725T>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145492763 | ||||||
chr4:145493101
|
C | G | 1 | a0001c0001t0017g0164 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-177+11063C>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145493101 | ||||||
chr4:145493115
|
A | G | 194 | a0001c0001t0001g0011a0001c0001t0001g0029a0001c0001t0001g0034others(191): Show | 205 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(202): Show |
intron_variant | MODIFIER | c.-177+11077A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145493115 | ||||||
chr4:145493288
|
G | A | 59 | a0001c0001t0001g0029a0001c0001t0001g0146a0001c0001t0004g0149others(56): Show | 61 | HG00438.hp1 HG01192.hp2 HG01243.hp1 others(58): Show |
intron_variant | MODIFIER | c.-177+11250G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145493288 | ||||||
chr4:145493321
|
T | C | 1 | a0001c0001t0013g0038 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-177+11283T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145493321 | ||||||
chr4:145493355
|
A | G | 1 | a0001c0002t0033g0075 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-177+11317A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145493355 | ||||||
chr4:145493448
|
G | T | 1 | a0001c0002t0033g0075 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-177+11410G>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145493448 | ||||||
chr4:145493639
|
G | A | 1 | a0001c0001t0004g0104 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-177+11601G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145493639 | ||||||
chr4:145493648
|
T | C | 2 | a0001c0001t0014g0039a0001c0001t0014g0071 | 2 | HG02145.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-177+11610T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145493648 | ||||||
chr4:145493736
|
C | G | 3 | a0001c0001t0017g0162a0001c0001t0017g0163a0001c0001t0017g0164 | 3 | HG02055.hp2 HG02280.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-177+11698C>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145493736 | ||||||
chr4:145493911
|
C | G | 5 | a0001c0001t0009g0286a0001c0001t0017g0162a0001c0001t0017g0163others(2): Show | 5 | HG02055.hp2 HG02280.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.-177+11873C>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145493911 | ||||||
chr4:145493971
|
A | AT | 4 | a0001c0001t0004g0007a0001c0001t0004g0116a0001c0001t0004g0117others(1): Show | 5 | HG02602.hp2 HG03017.hp1 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.-177+11941dupT | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 145493971 | |||||
chr4:145494013
|
G | A | 1 | a0001c0001t0004g0104 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-177+11975G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145494013 | ||||||
chr4:145494082
|
A | G | 1 | a0001c0002t0012g0050 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-177+12044A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145494082 | ||||||
chr4:145494128
|
GT | G | 32 | a0001c0001t0001g0029a0001c0001t0001g0146a0001c0001t0004g0149others(29): Show | 33 | HG00438.hp1 HG01243.hp1 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.-177+12095delT | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 145494128 | |||||
chr4:145494199
|
A | T | 59 | a0001c0001t0001g0029a0001c0001t0001g0146a0001c0001t0004g0149others(56): Show | 61 | HG00438.hp1 HG01192.hp2 HG01243.hp1 others(58): Show |
intron_variant | MODIFIER | c.-177+12161A>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145494199 | ||||||
chr4:145494252
|
G | A | 1 | a0001c0002t0033g0075 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-177+12214G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145494252 | ||||||
chr4:145494255
|
C | T | 1 | a0001c0001t0002g0204 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-177+12217C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145494255 | ||||||
chr4:145494281
|
G | A | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG02135.hp1 HG04228.hp1 NA18945.hp1 others(1): Show |
intron_variant | MODIFIER | c.-177+12243G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145494281 | ||||||
chr4:145494486
|
G | T | 12 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0098others(9): Show | 12 | HG00423.hp1 HG00558.hp2 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.-177+12448G>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145494486 | ||||||
chr4:145494493
|
G | A | 1 | a0001c0001t0002g0214 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-177+12455G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145494493 | ||||||
chr4:145494660
|
A | G | 1 | a0001c0001t0002g0196 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-177+12622A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145494660 | ||||||
chr4:145494679
|
G | A | 2 | a0001c0001t0014g0066a0001c0001t0014g0067 | 2 | HG02451.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-177+12641G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145494679 | ||||||
chr4:145494783
|
T | C | 7 | a0001c0001t0001g0029a0001c0001t0007g0005a0001c0001t0007g0019others(4): Show | 8 | HG01261.hp1 HG02630.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.-177+12745T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145494783 | ||||||
chr4:145494936
|
A | G | 2 | a0001c0001t0004g0231a0001c0001t0004g0232 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-177+12898A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145494936 | ||||||
chr4:145494983
|
C | T | 2 | a0001c0001t0014g0039a0001c0001t0014g0071 | 2 | HG02145.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-177+12945C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145494983 | ||||||
chr4:145494990
|
T | A | 1 | a0001c0001t0002g0168 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-177+12952T>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145494990 | ||||||
chr4:145495078
|
G | A | 2 | a0001c0001t0014g0039a0001c0001t0014g0071 | 2 | HG02145.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-177+13040G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145495078 | ||||||
chr4:145495116
|
G | A | 10 | a0001c0001t0008g0016a0001c0001t0008g0051a0001c0001t0008g0155others(7): Show | 11 | HG01192.hp2 HG01496.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.-177+13078G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145495116 | ||||||
chr4:145495134
|
G | A | 49 | a0001c0001t0001g0029a0001c0001t0001g0146a0001c0001t0004g0149others(46): Show | 51 | HG00438.hp1 HG01192.hp2 HG01243.hp1 others(48): Show |
intron_variant | MODIFIER | c.-177+13096G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145495134 | ||||||
chr4:145495206
|
G | A | 1 | a0001c0001t0001g0266 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-177+13168G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145495206 | ||||||
chr4:145495253
|
G | A | 169 | a0001c0001t0001g0029a0001c0001t0001g0052a0001c0001t0001g0078others(166): Show | 179 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.-177+13215G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145495253 | ||||||
chr4:145495257
|
C | G | 2 | a0001c0001t0014g0039a0001c0001t0014g0071 | 2 | HG02145.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-177+13219C>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145495257 | ||||||
chr4:145495279
|
G | A | 5 | a0001c0001t0011g0040a0001c0001t0011g0041a0001c0001t0011g0073others(2): Show | 5 | HG02559.hp1 HG02647.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-177+13241G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145495279 | ||||||
chr4:145495298
|
A | G | 3 | a0001c0002t0012g0050a0001c0002t0012g0069a0001c0002t0012g0143 | 3 | HG02145.hp1 HG02257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-177+13260A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145495298 | ||||||
chr4:145495341
|
A | G | 4 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(1): Show | 4 | HG01243.hp1 HG02258.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.-177+13303A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145495341 | ||||||
chr4:145495383
|
A | G | 24 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(21): Show | 26 | HG00423.hp2 HG00621.hp1 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.-177+13345A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145495383 | ||||||
chr4:145495450
|
G | C | 1 | a0001c0002t0012g0143 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-177+13412G>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145495450 | ||||||
chr4:145495459
|
T | C | 16 | a0001c0001t0002g0001a0001c0001t0002g0063a0001c0001t0002g0081others(13): Show | 18 | HG00408.hp2 HG00544.hp2 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.-177+13421T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145495459 | ||||||
chr4:145495492
|
C | T | 2 | a0001c0001t0014g0039a0001c0001t0014g0071 | 2 | HG02145.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-177+13454C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145495492 | ||||||
chr4:145495537
|
G | A | 10 | a0001c0001t0008g0016a0001c0001t0008g0051a0001c0001t0008g0155others(7): Show | 11 | HG01192.hp2 HG01496.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.-177+13499G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145495537 | ||||||
chr4:145495616
|
C | CT | 17 | a0001c0001t0004g0105a0001c0001t0006g0225a0001c0001t0008g0016others(14): Show | 18 | HG01192.hp2 HG01496.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.-177+13597dupT | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 145495616 | |||||
chr4:145495616
|
C | CTT | 31 | a0001c0001t0001g0029a0001c0001t0001g0146a0001c0001t0004g0149others(28): Show | 32 | HG00438.hp1 HG01243.hp1 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.-177+13596_-177+13 others(8): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 145495616 | |||||
chr4:145495701
|
G | A | 8 | a0001c0001t0001g0146a0001c0001t0004g0149a0001c0001t0004g0150others(5): Show | 8 | HG01243.hp1 HG02258.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.-177+13663G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145495701 | ||||||
chr4:145495779
|
C | CT | 12 | a0001c0001t0002g0084a0001c0001t0006g0118a0001c0001t0006g0119others(9): Show | 12 | HG00738.hp2 HG01081.hp2 HG03654.hp1 others(9): Show |
intron_variant | MODIFIER | c.-177+13760dupT | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 145495779 | |||||
chr4:145495779
|
C | CTTTTT | 45 | a0001c0001t0001g0029a0001c0001t0001g0146a0001c0001t0004g0149others(42): Show | 47 | HG00438.hp1 HG01192.hp2 HG01243.hp1 others(44): Show |
intron_variant | MODIFIER | c.-177+13756_-177+13 others(11): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 145495779 | |||||
chr4:145495779
|
C | CTTTTTT | 9 | a0001c0001t0005g0026a0001c0001t0005g0049a0001c0001t0005g0106others(6): Show | 9 | HG02040.hp1 HG02135.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.-177+13755_-177+13 others(12): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 145495779 | |||||
chr4:145495881
|
A | G | 2 | a0001c0001t0020g0077a0001c0001t0020g0153 | 2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-177+13843A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145495881 | ||||||
chr4:145495984
|
A | G | 1 | a0001c0001t0001g0195 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-177+13946A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145495984 | ||||||
chr4:145495998
|
A | G | 2 | a0001c0001t0014g0039a0001c0001t0014g0071 | 2 | HG02145.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-177+13960A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145495998 | ||||||
chr4:145496085
|
A | T | 59 | a0001c0001t0001g0029a0001c0001t0001g0146a0001c0001t0004g0149others(56): Show | 61 | HG00438.hp1 HG01192.hp2 HG01243.hp1 others(58): Show |
intron_variant | MODIFIER | c.-177+14047A>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145496085 | ||||||
chr4:145496164
|
A | G | 1 | a0001c0001t0004g0152 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-177+14126A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145496164 | ||||||
chr4:145496276
|
G | C | 1 | a0001c0001t0001g0177 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-177+14238G>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145496276 | ||||||
chr4:145496357
|
A | G | 2 | a0001c0001t0014g0039a0001c0001t0014g0071 | 2 | HG02145.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-177+14319A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145496357 | ||||||
chr4:145496481
|
T | A | 3 | a0001c0001t0005g0023a0001c0001t0005g0024a0001c0001t0005g0045 | 3 | HG01884.hp2 HG03130.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-177+14443T>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145496481 | ||||||
chr4:145496545
|
G | T | 58 | a0001c0001t0001g0146a0001c0001t0004g0149a0001c0001t0004g0150others(55): Show | 60 | HG00438.hp1 HG01192.hp2 HG01243.hp1 others(57): Show |
intron_variant | MODIFIER | c.-177+14507G>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145496545 | ||||||
chr4:145496620
|
T | C | 58 | a0001c0001t0001g0146a0001c0001t0004g0149a0001c0001t0004g0150others(55): Show | 60 | HG00438.hp1 HG01192.hp2 HG01243.hp1 others(57): Show |
intron_variant | MODIFIER | c.-177+14582T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145496620 | ||||||
chr4:145496954
|
A | G | 1 | a0001c0001t0001g0141 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-177+14916A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145496954 | ||||||
chr4:145497015
|
A | G | 58 | a0001c0001t0001g0146a0001c0001t0004g0149a0001c0001t0004g0150others(55): Show | 60 | HG00438.hp1 HG01192.hp2 HG01243.hp1 others(57): Show |
intron_variant | MODIFIER | c.-177+14977A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145497015 | ||||||
chr4:145497036
|
A | G | 1 | a0001c0001t0004g0115 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-177+14998A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145497036 | ||||||
chr4:145497242
|
A | T | 1 | a0001c0001t0030g0142 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-177+15204A>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145497242 | ||||||
chr4:145497274
|
T | G | 2 | a0001c0001t0020g0077a0001c0001t0020g0153 | 2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-177+15236T>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145497274 | ||||||
chr4:145497295
|
T | C | 1 | a0001c0001t0003g0241 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-177+15257T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145497295 | ||||||
chr4:145497368
|
G | A | 5 | a0001c0001t0008g0016a0001c0001t0008g0051a0001c0001t0008g0155others(2): Show | 6 | HG01192.hp2 HG01496.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.-177+15330G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145497368 | ||||||
chr4:145497379
|
C | T | 1 | a0001c0001t0002g0280 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-177+15341C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145497379 | ||||||
chr4:145497403
|
G | C | 58 | a0001c0001t0001g0146a0001c0001t0004g0149a0001c0001t0004g0150others(55): Show | 60 | HG00438.hp1 HG01192.hp2 HG01243.hp1 others(57): Show |
intron_variant | MODIFIER | c.-177+15365G>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145497403 | ||||||
chr4:145497635
|
C | T | 3 | a0001c0002t0012g0050a0001c0002t0012g0069a0001c0002t0012g0143 | 3 | HG02145.hp1 HG02257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-177+15597C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145497635 | ||||||
chr4:145497649
|
T | C | 1 | a0001c0001t0001g0265 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-177+15611T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145497649 | ||||||
chr4:145497695
|
T | C | 172 | a0001c0001t0001g0034a0001c0001t0001g0052a0001c0001t0001g0064others(169): Show | 182 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(179): Show |
intron_variant | MODIFIER | c.-177+15657T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145497695 | ||||||
chr4:145497747
|
C | G | 2 | a0001c0001t0014g0039a0001c0001t0014g0071 | 2 | HG02145.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-177+15709C>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145497747 | ||||||
chr4:145497771
|
T | G | 2 | a0001c0001t0021g0027a0001c0001t0021g0028 | 2 | HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-177+15733T>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145497771 | ||||||
chr4:145497870
|
G | A | 5 | a0001c0001t0011g0040a0001c0001t0011g0041a0001c0001t0011g0073others(2): Show | 5 | HG02559.hp1 HG02647.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-177+15832G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145497870 | ||||||
chr4:145497883
|
A | G | 5 | a0001c0001t0008g0016a0001c0001t0008g0051a0001c0001t0008g0155others(2): Show | 6 | HG01192.hp2 HG01496.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.-177+15845A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145497883 | ||||||
chr4:145498035
|
T | A | 2 | a0001c0001t0014g0039a0001c0001t0014g0071 | 2 | HG02145.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-177+15997T>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145498035 | ||||||
chr4:145498245
|
C | T | 1 | a0001c0001t0001g0276 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-176-16193C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145498245 | ||||||
chr4:145498928
|
C | A | 10 | a0001c0001t0011g0040a0001c0001t0011g0041a0001c0001t0011g0073others(7): Show | 10 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.-176-15510C>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145498928 | ||||||
chr4:145499093
|
T | C | 48 | a0001c0001t0001g0146a0001c0001t0004g0149a0001c0001t0004g0150others(45): Show | 50 | HG00438.hp1 HG01192.hp2 HG01243.hp1 others(47): Show |
intron_variant | MODIFIER | c.-176-15345T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145499093 | ||||||
chr4:145499186
|
G | A | 5 | a0001c0001t0009g0286a0001c0001t0017g0162a0001c0001t0017g0163others(2): Show | 5 | HG02055.hp2 HG02280.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.-176-15252G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145499186 | ||||||
chr4:145499348
|
C | G | 10 | a0001c0001t0008g0016a0001c0001t0008g0051a0001c0001t0008g0155others(7): Show | 11 | HG01192.hp2 HG01496.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.-176-15090C>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145499348 | ||||||
chr4:145499355
|
G | A | 5 | a0001c0001t0011g0040a0001c0001t0011g0041a0001c0001t0011g0073others(2): Show | 5 | HG02559.hp1 HG02647.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-176-15083G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145499355 | ||||||
chr4:145499424
|
C | G | 2 | a0001c0003t0012g0072a0001c0003t0012g0144 | 2 | HG01884.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.-176-15014C>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145499424 | ||||||
chr4:145499436
|
T | A | 2 | a0001c0003t0012g0072a0001c0003t0012g0144 | 2 | HG01884.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.-176-15002T>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145499436 | ||||||
chr4:145499715
|
T | G | 3 | a0001c0002t0012g0050a0001c0002t0012g0069a0001c0002t0012g0143 | 3 | HG02145.hp1 HG02257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-176-14723T>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145499715 | ||||||
chr4:145499843
|
A | G | 4 | a0001c0001t0017g0162a0001c0001t0017g0163a0001c0001t0017g0164others(1): Show | 4 | HG02055.hp2 HG02280.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-176-14595A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145499843 | ||||||
chr4:145499933
|
G | A | 58 | a0001c0001t0001g0146a0001c0001t0004g0149a0001c0001t0004g0150others(55): Show | 60 | HG00438.hp1 HG01192.hp2 HG01243.hp1 others(57): Show |
intron_variant | MODIFIER | c.-176-14505G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145499933 | ||||||
chr4:145499995
|
A | C | 3 | a0001c0001t0009g0286a0001c0001t0020g0077a0001c0001t0020g0153 | 3 | HG02895.hp1 HG03540.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-176-14443A>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145499995 | ||||||
chr4:145500335
|
C | T | 2 | a0001c0001t0020g0077a0001c0001t0020g0153 | 2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-176-14103C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145500335 | ||||||
chr4:145500380
|
C | A | 1 | a0001c0001t0003g0015 | 2 | HG00642.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-176-14058C>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145500380 | ||||||
chr4:145500412
|
G | A | 1 | a0001c0002t0033g0075 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-176-14026G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145500412 | ||||||
chr4:145500531
|
C | T | 1 | a0001c0002t0033g0075 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-176-13907C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145500531 | ||||||
chr4:145500550
|
A | G | 97 | a0001c0001t0001g0052a0001c0001t0001g0078a0001c0001t0001g0103others(94): Show | 101 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(98): Show |
intron_variant | MODIFIER | c.-176-13888A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145500550 | ||||||
chr4:145500552
|
G | A | 5 | a0001c0001t0001g0100a0001c0001t0001g0205a0001c0001t0004g0206others(2): Show | 5 | HG02717.hp1 HG02809.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-176-13886G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145500552 | ||||||
chr4:145500555
|
G | A | 2 | a0001c0001t0021g0027a0001c0001t0021g0028 | 2 | HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-176-13883G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145500555 | ||||||
chr4:145500716
|
T | G | 1 | a0001c0001t0004g0053 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-176-13722T>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145500716 | ||||||
chr4:145500984
|
G | A | 5 | a0001c0001t0011g0040a0001c0001t0011g0041a0001c0001t0011g0073others(2): Show | 5 | HG02559.hp1 HG02647.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-176-13454G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145500984 | ||||||
chr4:145501021
|
G | A | 3 | a0001c0002t0012g0050a0001c0002t0012g0069a0001c0002t0012g0143 | 3 | HG02145.hp1 HG02257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-176-13417G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145501021 | ||||||
chr4:145501514
|
G | A | 2 | a0001c0001t0021g0027a0001c0001t0021g0028 | 2 | HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-176-12924G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145501514 | ||||||
chr4:145501533
|
A | G | 78 | a0001c0001t0001g0052a0001c0001t0001g0078a0001c0001t0001g0122others(75): Show | 81 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.-176-12905A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145501533 | ||||||
chr4:145501552
|
G | A | 2 | a0001c0003t0012g0072a0001c0003t0012g0144 | 2 | HG01884.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.-176-12886G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145501552 | ||||||
chr4:145501641
|
CT | C | 90 | a0001c0001t0001g0052a0001c0001t0001g0122a0001c0001t0001g0138others(87): Show | 95 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(92): Show |
intron_variant | MODIFIER | c.-176-12784delT | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 145501641 | |||||
chr4:145501721
|
CT | C | 53 | a0001c0001t0001g0249a0001c0001t0003g0003a0001c0001t0003g0004others(50): Show | 59 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.-176-12705delT | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 145501721 | |||||
chr4:145501881
|
C | G | 168 | a0001c0001t0001g0052a0001c0001t0001g0078a0001c0001t0001g0122others(165): Show | 178 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(175): Show |
intron_variant | MODIFIER | c.-176-12557C>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145501881 | ||||||
chr4:145501989
|
C | T | 2 | a0001c0001t0014g0039a0001c0001t0014g0071 | 2 | HG02145.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-176-12449C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145501989 | ||||||
chr4:145502065
|
C | T | 2 | a0001c0001t0014g0039a0001c0001t0014g0071 | 2 | HG02145.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-176-12373C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145502065 | ||||||
chr4:145502123
|
A | G | 1 | a0001c0001t0030g0142 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-176-12315A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145502123 | ||||||
chr4:145502229
|
G | C | 3 | a0001c0001t0003g0135a0001c0001t0003g0258a0001c0001t0016g0257 | 3 | HG01175.hp2 HG01257.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.-176-12209G>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145502229 | ||||||
chr4:145502246
|
A | G | 103 | a0001c0001t0001g0052a0001c0001t0001g0078a0001c0001t0001g0122others(100): Show | 107 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(104): Show |
intron_variant | MODIFIER | c.-176-12192A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145502246 | ||||||
chr4:145502267
|
C | T | 17 | a0001c0001t0008g0016a0001c0001t0008g0051a0001c0001t0008g0155others(14): Show | 18 | HG01192.hp2 HG01496.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.-176-12171C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145502267 | ||||||
chr4:145502363
|
T | G | 103 | a0001c0001t0001g0052a0001c0001t0001g0078a0001c0001t0001g0122others(100): Show | 107 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(104): Show |
intron_variant | MODIFIER | c.-176-12075T>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145502363 | ||||||
chr4:145502399
|
A | T | 2 | a0001c0001t0014g0039a0001c0001t0014g0071 | 2 | HG02145.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-176-12039A>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145502399 | ||||||
chr4:145502427
|
A | G | 5 | a0001c0001t0011g0040a0001c0001t0011g0041a0001c0001t0011g0073others(2): Show | 5 | HG02559.hp1 HG02647.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-176-12011A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145502427 | ||||||
chr4:145502534
|
A | G | 1 | a0001c0001t0004g0104 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-176-11904A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145502534 | ||||||
chr4:145502628
|
A | G | 1 | a0001c0001t0009g0286 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-176-11810A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145502628 | ||||||
chr4:145502649
|
C | T | 1 | a0001c0001t0014g0071 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-176-11789C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145502649 | ||||||
chr4:145502775
|
A | T | 2 | a0001c0001t0002g0095a0001c0001t0002g0194 | 2 | HG00099.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.-176-11663A>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145502775 | ||||||
chr4:145502823
|
A | G | 27 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(24): Show | 28 | HG00438.hp1 HG01243.hp1 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.-176-11615A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145502823 | ||||||
chr4:145502837
|
G | A | 1 | a0001c0001t0001g0178 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-176-11601G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145502837 | ||||||
chr4:145502912
|
G | A | 1 | a0001c0002t0033g0075 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-176-11526G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145502912 | ||||||
chr4:145502956
|
TCAGTGTC others(15): Show |
T | 1 | a0001c0001t0002g0176 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-176-11463_-176-11 others(28): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 145502956 | |||||
chr4:145502989
|
G | A | 2 | a0001c0001t0020g0077a0001c0001t0020g0153 | 2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-176-11449G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145502989 | ||||||
chr4:145503403
|
C | T | 2 | a0001c0001t0020g0077a0001c0001t0020g0153 | 2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-176-11035C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145503403 | ||||||
chr4:145503422
|
C | T | 12 | a0001c0001t0006g0118a0001c0001t0006g0119a0001c0001t0006g0120others(9): Show | 12 | HG00738.hp2 HG01081.hp2 HG03654.hp1 others(9): Show |
intron_variant | MODIFIER | c.-176-11016C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145503422 | ||||||
chr4:145503677
|
A | G | 3 | a0001c0001t0006g0222a0001c0001t0006g0223a0001c0001t0006g0224 | 3 | HG01081.hp2 HG03942.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-176-10761A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145503677 | ||||||
chr4:145504071
|
C | T | 8 | a0001c0001t0020g0077a0001c0001t0020g0153a0001c0002t0012g0050others(5): Show | 8 | HG01884.hp1 HG02109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.-176-10367C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145504071 | ||||||
chr4:145504238
|
T | C | 1 | a0001c0001t0026g0213 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-176-10200T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145504238 | ||||||
chr4:145504303
|
A | G | 1 | a0001c0001t0001g0157 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-176-10135A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145504303 | ||||||
chr4:145504391
|
C | A | 2 | a0001c0001t0003g0014a0001c0001t0003g0137 | 3 | HG01099.hp1 HG01255.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.-176-10047C>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145504391 | ||||||
chr4:145504453
|
C | T | 5 | a0001c0001t0011g0040a0001c0001t0011g0041a0001c0001t0011g0073others(2): Show | 5 | HG02559.hp1 HG02647.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-176-9985C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145504453 | ||||||
chr4:145504464
|
G | A | 1 | a0001c0001t0003g0282 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-176-9974G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145504464 | ||||||
chr4:145504467
|
C | T | 16 | a0001c0001t0005g0020a0001c0001t0005g0021a0001c0001t0005g0022others(13): Show | 16 | HG00438.hp1 HG01243.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.-176-9971C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145504467 | ||||||
chr4:145504528
|
G | A | 3 | a0001c0002t0012g0050a0001c0002t0012g0069a0001c0002t0012g0143 | 3 | HG02145.hp1 HG02257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-176-9910G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145504528 | ||||||
chr4:145504671
|
T | A | 4 | a0001c0001t0014g0039a0001c0001t0014g0066a0001c0001t0014g0067others(1): Show | 4 | HG02145.hp2 HG02451.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-176-9767T>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145504671 | ||||||
chr4:145504748
|
T | G | 1 | a0001c0001t0031g0284 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-176-9690T>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145504748 | ||||||
chr4:145504841
|
C | T | 6 | a0001c0002t0012g0050a0001c0002t0012g0069a0001c0002t0012g0143others(3): Show | 6 | HG01884.hp1 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.-176-9597C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145504841 | ||||||
chr4:145504862
|
C | G | 1 | a0001c0001t0001g0018 | 2 | HG01928.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.-176-9576C>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145504862 | ||||||
chr4:145504949
|
G | A | 1 | a0001c0001t0004g0116 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-176-9489G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145504949 | ||||||
chr4:145504955
|
C | G | 87 | a0001c0001t0001g0034a0001c0001t0001g0052a0001c0001t0001g0064others(84): Show | 90 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(87): Show |
intron_variant | MODIFIER | c.-176-9483C>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145504955 | ||||||
chr4:145504990
|
G | A | 6 | a0001c0002t0012g0050a0001c0002t0012g0069a0001c0002t0012g0143others(3): Show | 6 | HG01884.hp1 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.-176-9448G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145504990 | ||||||
chr4:145505048
|
A | G | 1 | a0001c0001t0004g0114 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-176-9390A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145505048 | ||||||
chr4:145505056
|
T | C | 1 | a0001c0001t0001g0215 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-176-9382T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145505056 | ||||||
chr4:145505162
|
T | C | 53 | a0001c0001t0001g0249a0001c0001t0003g0003a0001c0001t0003g0004others(50): Show | 59 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.-176-9276T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145505162 | ||||||
chr4:145505174
|
T | C | 1 | a0001c0001t0009g0233 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-176-9264T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145505174 | ||||||
chr4:145505198
|
C | T | 3 | a0001c0002t0012g0050a0001c0002t0012g0069a0001c0002t0012g0143 | 3 | HG02145.hp1 HG02257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-176-9240C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145505198 | ||||||
chr4:145505367
|
T | C | 1 | a0001c0001t0001g0264 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-176-9071T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145505367 | ||||||
chr4:145505575
|
C | T | 1 | a0001c0001t0001g0193 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-176-8863C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145505575 | ||||||
chr4:145505610
|
C | G | 1 | a0001c0001t0001g0195 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-176-8828C>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145505610 | ||||||
chr4:145505616
|
C | CA | 14 | a0001c0001t0002g0227a0001c0001t0002g0267a0001c0001t0003g0256others(11): Show | 14 | HG01433.hp1 HG01934.hp2 HG01981.hp1 others(11): Show |
intron_variant | MODIFIER | c.-176-8805dupA | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 145505616 | |||||
chr4:145505616
|
CA | C | 39 | a0001c0001t0001g0210a0001c0001t0004g0006a0001c0001t0004g0109others(36): Show | 41 | HG00423.hp2 HG00438.hp1 HG01243.hp1 others(38): Show |
intron_variant | MODIFIER | c.-176-8805delA | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 145505616 | |||||
chr4:145505616
|
CAA | C | 47 | a0001c0001t0001g0052a0001c0001t0001g0078a0001c0001t0001g0122others(44): Show | 48 | HG00621.hp1 HG01081.hp1 HG01175.hp1 others(45): Show |
intron_variant | MODIFIER | c.-176-8806_-176-880 others(6): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 145505616 | |||||
chr4:145505626
|
A | G | 2 | a0001c0001t0019g0219a0001c0001t0027g0279 | 2 | HG03927.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-176-8812A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145505626 | ||||||
chr4:145505675
|
T | G | 1 | a0001c0001t0001g0160 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-176-8763T>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145505675 | ||||||
chr4:145505767
|
G | A | 2 | a0001c0001t0002g0010a0001c0001t0002g0179 | 3 | NA18960.hp1 NA18975.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.-176-8671G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145505767 | ||||||
chr4:145505792
|
A | G | 2 | a0001c0003t0012g0072a0001c0003t0012g0144 | 2 | HG01884.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.-176-8646A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145505792 | ||||||
chr4:145505796
|
G | A | 3 | a0001c0002t0012g0050a0001c0002t0012g0069a0001c0002t0012g0143 | 3 | HG02145.hp1 HG02257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-176-8642G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145505796 | ||||||
chr4:145505879
|
C | T | 1 | a0001c0002t0033g0075 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-176-8559C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145505879 | ||||||
chr4:145505932
|
C | T | 2 | a0001c0003t0012g0072a0001c0003t0012g0144 | 2 | HG01884.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.-176-8506C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145505932 | ||||||
chr4:145506259
|
T | C | 1 | a0001c0002t0033g0075 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-176-8179T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145506259 | ||||||
chr4:145506399
|
C | T | 76 | a0001c0001t0001g0052a0001c0001t0001g0078a0001c0001t0001g0122others(73): Show | 79 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.-176-8039C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145506399 | ||||||
chr4:145506689
|
T | TA | 5 | a0001c0001t0002g0084a0001c0001t0007g0030a0001c0001t0007g0154others(2): Show | 5 | HG01261.hp1 HG02630.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-176-7740dupA | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 145506689 | |||||
chr4:145506730
|
T | C | 3 | a0001c0002t0012g0050a0001c0002t0012g0069a0001c0002t0012g0143 | 3 | HG02145.hp1 HG02257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-176-7708T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145506730 | ||||||
chr4:145506957
|
C | T | 3 | a0001c0002t0012g0050a0001c0002t0012g0069a0001c0002t0012g0143 | 3 | HG02145.hp1 HG02257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-176-7481C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145506957 | ||||||
chr4:145506965
|
A | G | 1 | a0001c0001t0004g0104 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-176-7473A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145506965 | ||||||
chr4:145506965
|
A | T | 4 | a0001c0001t0005g0021a0001c0001t0005g0043a0001c0001t0005g0044others(1): Show | 4 | HG00438.hp1 HG02135.hp2 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.-176-7473A>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145506965 | ||||||
chr4:145507068
|
A | G | 5 | a0001c0001t0003g0127a0001c0001t0003g0238a0001c0001t0003g0239others(2): Show | 5 | HG00438.hp2 NA19057.hp1 NA19065.hp2 others(2): Show |
intron_variant | MODIFIER | c.-176-7370A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145507068 | ||||||
chr4:145507134
|
G | C | 1 | a0001c0001t0009g0235 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-176-7304G>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145507134 | ||||||
chr4:145507175
|
G | GT | 18 | a0001c0001t0002g0084a0001c0001t0004g0111a0001c0001t0006g0118others(15): Show | 19 | HG00738.hp2 HG01081.hp2 HG02895.hp1 others(16): Show |
intron_variant | MODIFIER | c.-176-7251dupT | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 145507175 | |||||
chr4:145507175
|
G | T | 1 | a0001c0001t0004g0108 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-176-7263G>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145507175 | ||||||
chr4:145507176
|
T | G | 2 | a0001c0001t0014g0066a0001c0001t0014g0067 | 2 | HG02451.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-176-7262T>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145507176 | ||||||
chr4:145507232
|
A | G | 225 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0018others(222): Show | 238 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(235): Show |
intron_variant | MODIFIER | c.-176-7206A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145507232 | ||||||
chr4:145507369
|
C | T | 1 | a0001c0001t0001g0056 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-176-7069C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145507369 | ||||||
chr4:145507681
|
T | C | 1 | a0001c0001t0003g0015 | 2 | HG00642.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-176-6757T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145507681 | ||||||
chr4:145507979
|
A | C | 3 | a0001c0001t0001g0034a0001c0001t0001g0064a0001c0001t0001g0065 | 3 | HG02622.hp1 HG03209.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-176-6459A>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145507979 | ||||||
chr4:145508013
|
TCG | T | 16 | a0001c0001t0005g0020a0001c0001t0005g0021a0001c0001t0005g0022others(13): Show | 16 | HG00438.hp1 HG01243.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.-176-6424_-176-642 others(6): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145508013 | ||||||
chr4:145508065
|
A | C | 1 | a0001c0001t0005g0042 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-176-6373A>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145508065 | ||||||
chr4:145508080
|
A | AT | 17 | a0001c0001t0001g0192a0001c0001t0002g0084a0001c0001t0002g0186others(14): Show | 17 | HG00438.hp1 HG00738.hp2 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.-176-6341dupT | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 145508080 | |||||
chr4:145508080
|
AT | A | 54 | a0001c0001t0001g0249a0001c0001t0001g0270a0001c0001t0003g0003others(51): Show | 59 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.-176-6341delT | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 145508080 | |||||
chr4:145508616
|
G | C | 2 | a0001c0001t0020g0077a0001c0001t0020g0153 | 2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-176-5822G>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145508616 | ||||||
chr4:145508640
|
T | A | 11 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(8): Show | 12 | HG01243.hp1 HG01261.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.-176-5798T>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145508640 | ||||||
chr4:145508804
|
G | A | 1 | a0001c0001t0002g0180 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-176-5634G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145508804 | ||||||
chr4:145508889
|
T | C | 6 | a0001c0002t0012g0050a0001c0002t0012g0069a0001c0002t0012g0143others(3): Show | 6 | HG01884.hp1 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.-176-5549T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145508889 | ||||||
chr4:145508951
|
C | G | 1 | a0001c0002t0033g0075 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-176-5487C>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145508951 | ||||||
chr4:145509103
|
C | T | 2 | a0001c0003t0012g0072a0001c0003t0012g0144 | 2 | HG01884.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.-176-5335C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145509103 | ||||||
chr4:145509133
|
T | G | 3 | a0001c0002t0012g0050a0001c0002t0012g0069a0001c0002t0012g0143 | 3 | HG02145.hp1 HG02257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-176-5305T>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145509133 | ||||||
chr4:145509141
|
T | G | 103 | a0001c0001t0001g0052a0001c0001t0001g0078a0001c0001t0001g0122others(100): Show | 107 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(104): Show |
intron_variant | MODIFIER | c.-176-5297T>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145509141 | ||||||
chr4:145509143
|
A | G | 1 | a0001c0002t0033g0075 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-176-5295A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145509143 | ||||||
chr4:145509381
|
C | T | 5 | a0001c0001t0009g0286a0001c0001t0017g0162a0001c0001t0017g0163others(2): Show | 5 | HG02055.hp2 HG02280.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.-176-5057C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145509381 | ||||||
chr4:145509382
|
G | A | 3 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151 | 3 | HG02258.hp2 HG02280.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.-176-5056G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145509382 | ||||||
chr4:145509518
|
C | T | 6 | a0001c0001t0007g0005a0001c0001t0007g0019a0001c0001t0007g0030others(3): Show | 7 | HG01261.hp1 HG02630.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.-176-4920C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145509518 | ||||||
chr4:145509654
|
G | A | 1 | a0001c0001t0001g0208 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-176-4784G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145509654 | ||||||
chr4:145509887
|
C | T | 1 | a0001c0001t0013g0037 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-176-4551C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145509887 | ||||||
chr4:145509888
|
G | A | 2 | a0001c0001t0005g0021a0001c0001t0005g0044 | 2 | HG00438.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.-176-4550G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145509888 | ||||||
chr4:145509949
|
G | T | 2 | a0001c0001t0002g0184a0001c0001t0002g0185 | 2 | HG01261.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-176-4489G>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145509949 | ||||||
chr4:145510002
|
A | G | 29 | a0001c0001t0001g0052a0001c0001t0001g0078a0001c0001t0001g0138others(26): Show | 31 | HG00423.hp2 HG00621.hp1 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.-176-4436A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145510002 | ||||||
chr4:145510396
|
A | G | 6 | a0001c0002t0012g0050a0001c0002t0012g0069a0001c0002t0012g0143others(3): Show | 6 | HG01884.hp1 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.-176-4042A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145510396 | ||||||
chr4:145510477
|
T | C | 26 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(23): Show | 28 | HG00423.hp2 HG00621.hp1 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.-176-3961T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145510477 | ||||||
chr4:145510706
|
T | G | 1 | a0001c0002t0033g0075 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-176-3732T>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145510706 | ||||||
chr4:145510729
|
G | C | 3 | a0001c0001t0002g0096a0001c0001t0002g0197a0001c0001t0002g0198 | 3 | NA18957.hp1 NA19002.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.-176-3709G>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145510729 | ||||||
chr4:145511015
|
C | T | 5 | a0001c0002t0012g0050a0001c0002t0012g0069a0001c0002t0012g0143others(2): Show | 5 | HG01884.hp1 HG02109.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.-176-3423C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145511015 | ||||||
chr4:145511096
|
T | C | 4 | a0001c0001t0004g0007a0001c0001t0004g0116a0001c0001t0004g0117others(1): Show | 5 | HG02602.hp2 HG03017.hp1 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.-176-3342T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145511096 | ||||||
chr4:145511194
|
T | C | 5 | a0001c0001t0011g0040a0001c0001t0011g0041a0001c0001t0011g0073others(2): Show | 5 | HG02559.hp1 HG02647.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-176-3244T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145511194 | ||||||
chr4:145511302
|
C | CA | 106 | a0001c0001t0001g0034a0001c0001t0001g0052a0001c0001t0001g0064others(103): Show | 110 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(107): Show |
intron_variant | MODIFIER | c.-176-3136_-176-313 others(5): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145511302 | ||||||
chr4:145511303
|
G | T | 1 | a0001c0001t0003g0240 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-176-3135G>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145511303 | ||||||
chr4:145511342
|
A | G | 5 | a0001c0001t0011g0040a0001c0001t0011g0041a0001c0001t0011g0073others(2): Show | 5 | HG02559.hp1 HG02647.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-176-3096A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145511342 | ||||||
chr4:145511692
|
C | T | 1 | a0001c0001t0002g0099 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-176-2746C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145511692 | ||||||
chr4:145511884
|
T | C | 4 | a0001c0001t0014g0039a0001c0001t0014g0066a0001c0001t0014g0067others(1): Show | 4 | HG02145.hp2 HG02451.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-176-2554T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145511884 | ||||||
chr4:145511928
|
T | C | 1 | a0001c0001t0003g0240 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-176-2510T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145511928 | ||||||
chr4:145511935
|
T | C | 4 | a0001c0001t0014g0039a0001c0001t0014g0066a0001c0001t0014g0067others(1): Show | 4 | HG02145.hp2 HG02451.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-176-2503T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145511935 | ||||||
chr4:145512059
|
C | T | 4 | a0001c0001t0014g0039a0001c0001t0014g0066a0001c0001t0014g0067others(1): Show | 4 | HG02145.hp2 HG02451.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-176-2379C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145512059 | ||||||
chr4:145512081
|
T | C | 1 | a0001c0001t0009g0286 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-176-2357T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145512081 | ||||||
chr4:145512263
|
C | T | 1 | a0001c0001t0004g0053 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-176-2175C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145512263 | ||||||
chr4:145512364
|
C | T | 79 | a0001c0001t0001g0034a0001c0001t0001g0052a0001c0001t0001g0064others(76): Show | 82 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.-176-2074C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145512364 | ||||||
chr4:145512634
|
C | T | 4 | a0001c0001t0001g0122a0001c0001t0001g0228a0001c0001t0001g0229others(1): Show | 4 | HG01891.hp1 HG03041.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-176-1804C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145512634 | ||||||
chr4:145512665
|
T | G | 2 | a0001c0001t0020g0077a0001c0001t0020g0153 | 2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-176-1773T>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145512665 | ||||||
chr4:145512928
|
G | T | 5 | a0001c0001t0011g0040a0001c0001t0011g0041a0001c0001t0011g0073others(2): Show | 5 | HG02559.hp1 HG02647.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-176-1510G>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145512928 | ||||||
chr4:145512940
|
C | A | 1 | a0001c0001t0016g0091 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-176-1498C>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145512940 | ||||||
chr4:145513046
|
G | A | 47 | a0001c0001t0001g0052a0001c0001t0001g0078a0001c0001t0001g0122others(44): Show | 49 | HG00423.hp2 HG00621.hp1 HG01081.hp1 others(46): Show |
intron_variant | MODIFIER | c.-176-1392G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145513046 | ||||||
chr4:145513077
|
C | T | 16 | a0001c0001t0005g0020a0001c0001t0005g0021a0001c0001t0005g0022others(13): Show | 16 | HG00438.hp1 HG01243.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.-176-1361C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145513077 | ||||||
chr4:145513200
|
C | T | 1 | a0001c0001t0015g0148 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-176-1238C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145513200 | ||||||
chr4:145513528
|
C | T | 47 | a0001c0001t0001g0052a0001c0001t0001g0078a0001c0001t0001g0122others(44): Show | 49 | HG00423.hp2 HG00621.hp1 HG01081.hp1 others(46): Show |
intron_variant | MODIFIER | c.-176-910C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145513528 | ||||||
chr4:145513550
|
T | A | 2 | a0001c0001t0021g0027a0001c0001t0021g0028 | 2 | HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-176-888T>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145513550 | ||||||
chr4:145513634
|
G | T | 8 | a0001c0001t0020g0077a0001c0001t0020g0153a0001c0002t0012g0050others(5): Show | 8 | HG01884.hp1 HG02109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.-176-804G>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145513634 | ||||||
chr4:145513911
|
T | C | 2 | a0001c0003t0012g0072a0001c0003t0012g0144 | 2 | HG01884.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.-176-527T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145513911 | ||||||
chr4:145513914
|
T | A | 2 | a0001c0003t0012g0072a0001c0003t0012g0144 | 2 | HG01884.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.-176-524T>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | chr4 | 145513914 | ||||||
chr4:145514222
|
TACTTA | T | 76 | a0001c0001t0001g0052a0001c0001t0001g0078a0001c0001t0001g0122others(73): Show | 79 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.-176-211_-176-207d others(7): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 145514222 | |||||
chr4:145515090
|
C | A | 6 | a0001c0002t0012g0050a0001c0002t0012g0069a0001c0002t0012g0143others(3): Show | 6 | HG01884.hp1 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.400+77C>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145515090 | ||||||
chr4:145515134
|
C | CTG | 64 | a0001c0001t0001g0054a0001c0001t0001g0064a0001c0001t0001g0065others(61): Show | 70 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.400+163_400+164dup others(2): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145515134 | |||||
chr4:145515134
|
C | CTGTG | 36 | a0001c0001t0001g0055a0001c0001t0001g0058a0001c0001t0001g0070others(33): Show | 37 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.400+161_400+164dup others(4): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145515134 | |||||
chr4:145515134
|
C | CTGTGTG | 23 | a0001c0001t0001g0034a0001c0001t0001g0100a0001c0001t0001g0103others(20): Show | 24 | HG01167.hp2 HG01169.hp1 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.400+159_400+164dup others(6): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145515134 | |||||
chr4:145515134
|
C | CTGTGTGT others(1): Show |
6 | a0001c0001t0001g0230a0001c0001t0003g0260a0001c0001t0004g0059others(3): Show | 6 | HG02735.hp1 HG02809.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.400+157_400+164dup others(8): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145515134 | |||||
chr4:145515134
|
C | CTGTGTGT others(5): Show |
1 | a0001c0001t0023g0128 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.400+153_400+164dup others(12): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145515134 | |||||
chr4:145515134
|
CTG | C | 56 | a0001c0001t0001g0009a0001c0001t0001g0107a0001c0001t0001g0156others(53): Show | 62 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.400+163_400+164del others(2): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145515134 | |||||
chr4:145515134
|
CTGTG | C | 9 | a0001c0001t0001g0052a0001c0001t0001g0078a0001c0001t0001g0165others(6): Show | 9 | HG01106.hp2 HG02109.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.400+161_400+164del others(4): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145515134 | |||||
chr4:145515134
|
CTGTGTG | C | 4 | a0001c0001t0001g0208a0001c0001t0002g0012a0001c0001t0005g0042others(1): Show | 5 | HG01981.hp2 HG02148.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.400+159_400+164del others(6): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145515134 | |||||
chr4:145515134
|
CTGTGTGT others(1): Show |
C | 3 | a0001c0001t0009g0286a0001c0001t0020g0077a0001c0001t0020g0153 | 3 | HG02895.hp1 HG03540.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.400+157_400+164del others(8): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145515134 | |||||
chr4:145515134
|
CTGTGTGT others(3): Show |
C | 4 | a0001c0001t0005g0046a0001c0002t0012g0050a0001c0002t0012g0069others(1): Show | 4 | HG02132.hp1 HG02145.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.400+155_400+164del others(10): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145515134 | |||||
chr4:145515134
|
CTGTGTGT others(5): Show |
C | 2 | a0001c0003t0012g0072a0001c0003t0012g0144 | 2 | HG01884.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.400+153_400+164del others(12): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145515134 | |||||
chr4:145515134
|
CTGTGTGT others(9): Show |
C | 1 | a0001c0001t0013g0038 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.400+149_400+164del others(16): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145515134 | |||||
chr4:145515147
|
T | C | 3 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160 | 3 | HG02135.hp1 NA18945.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.400+134T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145515147 | ||||||
chr4:145515170
|
G | GTGTGTC | 3 | a0001c0001t0006g0220a0001c0001t0006g0225a0001c0001t0019g0221 | 3 | HG03654.hp1 NA18952.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.400+162_400+163ins others(6): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145515170 | |||||
chr4:145515170
|
G | GTGTGTGT others(1): Show |
5 | a0001c0001t0006g0120a0001c0001t0006g0222a0001c0001t0006g0223others(2): Show | 5 | HG01081.hp2 HG03927.hp1 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.400+164_400+171dup others(8): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145515170 | |||||
chr4:145515170
|
G | GTGTGTGT others(3): Show |
2 | a0001c0001t0006g0218a0001c0001t0019g0219 | 2 | HG00738.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.400+164_400+165ins others(10): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145515170 | |||||
chr4:145515174
|
G | GTGTGTC | 3 | a0001c0001t0011g0073a0001c0001t0011g0074a0001c0001t0011g0145 | 3 | HG02647.hp2 HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.400+164_400+165ins others(6): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145515174 | |||||
chr4:145515199
|
A | G | 97 | a0001c0001t0001g0034a0001c0001t0001g0052a0001c0001t0001g0064others(94): Show | 101 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(98): Show |
intron_variant | MODIFIER | c.400+186A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145515199 | ||||||
chr4:145515208
|
G | A | 1 | a0001c0001t0004g0079 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.400+195G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145515208 | ||||||
chr4:145515259
|
G | A | 2 | a0001c0003t0012g0072a0001c0003t0012g0144 | 2 | HG01884.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.400+246G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145515259 | ||||||
chr4:145515324
|
T | G | 79 | a0001c0001t0001g0034a0001c0001t0001g0052a0001c0001t0001g0064others(76): Show | 82 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.400+311T>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145515324 | ||||||
chr4:145515342
|
T | C | 2 | a0001c0001t0001g0052a0001c0001t0001g0078 | 2 | HG02109.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.400+329T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145515342 | ||||||
chr4:145515384
|
A | C | 3 | a0001c0001t0001g0034a0001c0001t0001g0064a0001c0001t0001g0065 | 3 | HG02622.hp1 HG03209.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.400+371A>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145515384 | ||||||
chr4:145515446
|
A | G | 6 | a0001c0002t0012g0050a0001c0002t0012g0069a0001c0002t0012g0143others(3): Show | 6 | HG01884.hp1 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.400+433A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145515446 | ||||||
chr4:145515457
|
A | G | 1 | a0001c0001t0004g0104 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.400+444A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145515457 | ||||||
chr4:145515526
|
C | T | 6 | a0001c0002t0012g0050a0001c0002t0012g0069a0001c0002t0012g0143others(3): Show | 6 | HG01884.hp1 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.400+513C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145515526 | ||||||
chr4:145515540
|
G | A | 1 | a0001c0001t0030g0142 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.400+527G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145515540 | ||||||
chr4:145515561
|
A | G | 2 | a0001c0003t0012g0072a0001c0003t0012g0144 | 2 | HG01884.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.400+548A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145515561 | ||||||
chr4:145515664
|
A | G | 6 | a0001c0002t0012g0050a0001c0002t0012g0069a0001c0002t0012g0143others(3): Show | 6 | HG01884.hp1 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.400+651A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145515664 | ||||||
chr4:145515782
|
A | G | 3 | a0001c0002t0012g0050a0001c0002t0012g0069a0001c0002t0012g0143 | 3 | HG02145.hp1 HG02257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.400+769A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145515782 | ||||||
chr4:145515867
|
G | A | 3 | a0001c0002t0012g0050a0001c0002t0012g0069a0001c0002t0012g0143 | 3 | HG02145.hp1 HG02257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.400+854G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145515867 | ||||||
chr4:145515967
|
G | T | 1 | a0001c0001t0001g0275 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.400+954G>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145515967 | ||||||
chr4:145516070
|
C | G | 1 | a0001c0001t0004g0108 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.400+1057C>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145516070 | ||||||
chr4:145516239
|
T | C | 97 | a0001c0001t0001g0034a0001c0001t0001g0052a0001c0001t0001g0064others(94): Show | 101 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(98): Show |
intron_variant | MODIFIER | c.400+1226T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145516239 | ||||||
chr4:145516315
|
G | A | 1 | a0001c0001t0023g0242 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.400+1302G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145516315 | ||||||
chr4:145516346
|
G | T | 10 | a0001c0001t0008g0016a0001c0001t0008g0051a0001c0001t0008g0155others(7): Show | 11 | HG01192.hp2 HG01496.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.400+1333G>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145516346 | ||||||
chr4:145516354
|
T | C | 3 | a0001c0002t0012g0050a0001c0002t0012g0069a0001c0002t0012g0143 | 3 | HG02145.hp1 HG02257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.400+1341T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145516354 | ||||||
chr4:145516487
|
A | G | 1 | a0001c0001t0019g0221 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.400+1474A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145516487 | ||||||
chr4:145516489
|
T | A | 97 | a0001c0001t0001g0034a0001c0001t0001g0052a0001c0001t0001g0064others(94): Show | 101 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(98): Show |
intron_variant | MODIFIER | c.400+1476T>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145516489 | ||||||
chr4:145516560
|
C | T | 12 | a0001c0001t0006g0118a0001c0001t0006g0119a0001c0001t0006g0120others(9): Show | 12 | HG00738.hp2 HG01081.hp2 HG03654.hp1 others(9): Show |
intron_variant | MODIFIER | c.400+1547C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145516560 | ||||||
chr4:145516629
|
C | T | 5 | a0001c0001t0004g0053a0001c0001t0004g0079a0001c0001t0004g0080others(2): Show | 5 | HG02572.hp2 HG02895.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.400+1616C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145516629 | ||||||
chr4:145516643
|
T | C | 3 | a0001c0001t0002g0267a0001c0001t0002g0269a0001c0001t0002g0277 | 3 | NA18979.hp1 NA18984.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.400+1630T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145516643 | ||||||
chr4:145516664
|
G | A | 5 | a0001c0001t0009g0286a0001c0001t0017g0162a0001c0001t0017g0163others(2): Show | 5 | HG02055.hp2 HG02280.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.400+1651G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145516664 | ||||||
chr4:145516773
|
A | C | 1 | a0002c0004t0002g0174 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.400+1760A>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145516773 | ||||||
chr4:145516831
|
A | G | 1 | a0001c0001t0001g0159 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.400+1818A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145516831 | ||||||
chr4:145517065
|
C | G | 1 | a0001c0001t0002g0203 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.400+2052C>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145517065 | ||||||
chr4:145517116
|
C | T | 3 | a0001c0001t0002g0267a0001c0001t0002g0269a0001c0001t0002g0277 | 3 | NA18979.hp1 NA18984.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.400+2103C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145517116 | ||||||
chr4:145517129
|
A | G | 8 | a0001c0001t0020g0077a0001c0001t0020g0153a0001c0002t0012g0050others(5): Show | 8 | HG01884.hp1 HG02109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.400+2116A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145517129 | ||||||
chr4:145517495
|
T | A | 1 | a0001c0001t0002g0179 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.400+2482T>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145517495 | ||||||
chr4:145517512
|
G | A | 1 | a0001c0001t0004g0060 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.400+2499G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145517512 | ||||||
chr4:145517654
|
TTTGGCCA others(1637): Show |
T | 54 | a0001c0001t0001g0249a0001c0001t0003g0003a0001c0001t0003g0004others(51): Show | 60 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.400+2649_400+4292d others(2): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145517654 | |||||
chr4:145517731
|
A | G | 17 | a0001c0001t0004g0006a0001c0001t0004g0059a0001c0001t0004g0060others(14): Show | 18 | HG00423.hp2 HG00621.hp1 HG01175.hp1 others(15): Show |
intron_variant | MODIFIER | c.400+2718A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145517731 | ||||||
chr4:145518222
|
A | G | 6 | a0001c0002t0012g0050a0001c0002t0012g0069a0001c0002t0012g0143others(3): Show | 6 | HG01884.hp1 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.400+3209A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145518222 | ||||||
chr4:145518234
|
A | G | 2 | a0001c0001t0020g0077a0001c0001t0020g0153 | 2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.400+3221A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145518234 | ||||||
chr4:145518243
|
G | A | 1 | a0001c0001t0002g0214 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.400+3230G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145518243 | ||||||
chr4:145518279
|
G | A | 4 | a0001c0001t0013g0036a0001c0001t0013g0037a0001c0001t0013g0038others(1): Show | 4 | HG02735.hp1 HG03017.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.400+3266G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145518279 | ||||||
chr4:145518310
|
A | G | 1 | a0001c0002t0033g0075 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.400+3297A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145518310 | ||||||
chr4:145518350
|
G | A | 1 | a0001c0001t0001g0157 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.400+3337G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145518350 | ||||||
chr4:145518452
|
G | T | 3 | a0001c0001t0001g0011a0001c0001t0001g0102a0001c0001t0001g0210 | 4 | HG02486.hp1 HG02622.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.400+3439G>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145518452 | ||||||
chr4:145518500
|
AAT | A | 6 | a0001c0001t0007g0032a0001c0002t0012g0050a0001c0002t0012g0069others(3): Show | 6 | HG01884.hp1 HG02145.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.400+3489_400+3490d others(4): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145518500 | |||||
chr4:145518501
|
AT | A | 83 | a0001c0001t0001g0052a0001c0001t0001g0078a0001c0001t0001g0093others(80): Show | 86 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.400+3489delT | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145518501 | ||||||
chr4:145518502
|
T | A | 27 | a0001c0001t0006g0118a0001c0001t0006g0119a0001c0001t0006g0120others(24): Show | 28 | HG00738.hp2 HG01081.hp2 HG01192.hp2 others(25): Show |
intron_variant | MODIFIER | c.400+3489T>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145518502 | ||||||
chr4:145518517
|
T | G | 8 | a0001c0001t0020g0077a0001c0001t0020g0153a0001c0002t0012g0050others(5): Show | 8 | HG01884.hp1 HG02109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.400+3504T>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145518517 | ||||||
chr4:145518555
|
A | G | 1 | a0001c0001t0002g0204 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.400+3542A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145518555 | ||||||
chr4:145518567
|
A | G | 77 | a0001c0001t0001g0052a0001c0001t0001g0078a0001c0001t0001g0093others(74): Show | 80 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.400+3554A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145518567 | ||||||
chr4:145518652
|
A | C | 48 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0012others(45): Show | 52 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.400+3639A>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145518652 | ||||||
chr4:145518748
|
TCTG | T | 6 | a0001c0002t0012g0050a0001c0002t0012g0069a0001c0002t0012g0143others(3): Show | 6 | HG01884.hp1 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.400+3739_400+3741d others(5): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145518748 | |||||
chr4:145518829
|
G | A | 2 | a0001c0003t0012g0072a0001c0003t0012g0144 | 2 | HG01884.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.400+3816G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145518829 | ||||||
chr4:145518923
|
A | G | 99 | a0001c0001t0001g0052a0001c0001t0001g0078a0001c0001t0001g0093others(96): Show | 103 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(100): Show |
intron_variant | MODIFIER | c.400+3910A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145518923 | ||||||
chr4:145519088
|
C | CT | 38 | a0001c0001t0001g0065a0001c0001t0001g0122a0001c0001t0001g0156others(35): Show | 38 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.400+4100dupT | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145519088 | |||||
chr4:145519088
|
C | CTT | 21 | a0001c0001t0002g0099a0001c0001t0004g0059a0001c0001t0006g0119others(18): Show | 21 | HG00738.hp2 HG01081.hp2 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.400+4099_400+4100d others(4): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145519088 | |||||
chr4:145519088
|
C | CTTT | 9 | a0001c0001t0002g0088a0001c0001t0002g0280a0001c0001t0006g0118others(6): Show | 9 | HG00673.hp1 HG00673.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.400+4098_400+4100d others(5): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145519088 | |||||
chr4:145519088
|
CT | C | 9 | a0001c0001t0001g0216a0001c0001t0001g0271a0001c0001t0002g0063others(6): Show | 9 | HG01070.hp1 HG01167.hp1 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.400+4100delT | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145519088 | |||||
chr4:145519127
|
G | A | 3 | a0001c0001t0009g0286a0001c0003t0012g0072a0001c0003t0012g0144 | 3 | HG01884.hp1 HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.400+4114G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145519127 | ||||||
chr4:145519145
|
G | A | 2 | a0001c0001t0001g0272a0001c0001t0001g0278 | 2 | HG03704.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.400+4132G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145519145 | ||||||
chr4:145519240
|
C | T | 1 | a0001c0001t0002g0090 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.400+4227C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145519240 | ||||||
chr4:145519305
|
A | G | 3 | a0001c0002t0012g0050a0001c0002t0012g0069a0001c0002t0012g0143 | 3 | HG02145.hp1 HG02257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.400+4292A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145519305 | ||||||
chr4:145519337
|
C | G | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG02135.hp1 HG04228.hp1 NA18945.hp1 others(1): Show |
intron_variant | MODIFIER | c.400+4324C>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145519337 | ||||||
chr4:145519396
|
G | C | 54 | a0001c0001t0001g0249a0001c0001t0003g0003a0001c0001t0003g0004others(51): Show | 60 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.400+4383G>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145519396 | ||||||
chr4:145519397
|
AAC | A | 54 | a0001c0001t0001g0249a0001c0001t0003g0003a0001c0001t0003g0004others(51): Show | 60 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.400+4385_400+4386d others(4): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145519397 | ||||||
chr4:145519400
|
C | G | 54 | a0001c0001t0001g0249a0001c0001t0003g0003a0001c0001t0003g0004others(51): Show | 60 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.400+4387C>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145519400 | ||||||
chr4:145519402
|
T | A | 54 | a0001c0001t0001g0249a0001c0001t0003g0003a0001c0001t0003g0004others(51): Show | 60 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.400+4389T>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145519402 | ||||||
chr4:145519404
|
T | G | 54 | a0001c0001t0001g0249a0001c0001t0003g0003a0001c0001t0003g0004others(51): Show | 60 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.400+4391T>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145519404 | ||||||
chr4:145519405
|
T | G | 54 | a0001c0001t0001g0249a0001c0001t0003g0003a0001c0001t0003g0004others(51): Show | 60 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.400+4392T>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145519405 | ||||||
chr4:145519465
|
G | A | 2 | a0001c0001t0020g0077a0001c0001t0020g0153 | 2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.400+4452G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145519465 | ||||||
chr4:145519489
|
AT | A | 10 | a0001c0001t0001g0107a0001c0001t0001g0208a0001c0001t0001g0215others(7): Show | 10 | HG01070.hp1 HG01071.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.400+4490delT | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145519489 | |||||
chr4:145519644
|
T | C | 102 | a0001c0001t0001g0034a0001c0001t0001g0052a0001c0001t0001g0064others(99): Show | 106 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(103): Show |
intron_variant | MODIFIER | c.400+4631T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145519644 | ||||||
chr4:145519664
|
A | AAAG | 10 | a0001c0001t0013g0036a0001c0001t0013g0038a0001c0001t0020g0077others(7): Show | 10 | HG01884.hp1 HG02109.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.400+4653_400+4654i others(5): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145519664 | |||||
chr4:145519664
|
A | AAG | 158 | a0001c0001t0001g0052a0001c0001t0001g0078a0001c0001t0001g0093others(155): Show | 168 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(165): Show |
intron_variant | MODIFIER | c.400+4652_400+4653i others(4): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145519664 | |||||
chr4:145519846
|
C | T | 79 | a0001c0001t0001g0052a0001c0001t0001g0078a0001c0001t0001g0093others(76): Show | 82 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.400+4833C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145519846 | ||||||
chr4:145519943
|
G | T | 2 | a0001c0001t0011g0040a0001c0001t0011g0041 | 2 | HG02559.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.400+4930G>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145519943 | ||||||
chr4:145520156
|
A | C | 2 | a0001c0001t0003g0092a0001c0001t0016g0091 | 2 | HG00609.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.400+5143A>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145520156 | ||||||
chr4:145520288
|
A | C | 1 | a0001c0001t0035g0283 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.400+5275A>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145520288 | ||||||
chr4:145520578
|
A | G | 1 | a0001c0001t0030g0142 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.400+5565A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145520578 | ||||||
chr4:145520727
|
T | C | 2 | a0001c0001t0004g0136a0001c0001t0004g0259 | 2 | NA18944.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.400+5714T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145520727 | ||||||
chr4:145520729
|
A | C | 1 | a0001c0001t0001g0160 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.400+5716A>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145520729 | ||||||
chr4:145520798
|
C | T | 1 | a0001c0001t0004g0053 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.400+5785C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145520798 | ||||||
chr4:145520932
|
A | G | 1 | a0001c0001t0001g0094 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.400+5919A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145520932 | ||||||
chr4:145521049
|
G | A | 1 | a0001c0001t0003g0246 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.400+6036G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145521049 | ||||||
chr4:145521061
|
A | G | 2 | a0001c0001t0020g0077a0001c0001t0020g0153 | 2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.400+6048A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145521061 | ||||||
chr4:145521101
|
C | G | 1 | a0001c0001t0004g0151 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.400+6088C>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145521101 | ||||||
chr4:145521193
|
G | C | 3 | a0001c0001t0001g0100a0001c0001t0004g0206a0001c0001t0004g0207 | 3 | HG02717.hp1 HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.400+6180G>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145521193 | ||||||
chr4:145521194
|
G | A | 12 | a0001c0001t0006g0118a0001c0001t0006g0119a0001c0001t0006g0120others(9): Show | 12 | HG00738.hp2 HG01081.hp2 HG03654.hp1 others(9): Show |
intron_variant | MODIFIER | c.400+6181G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145521194 | ||||||
chr4:145521238
|
A | G | 1 | a0001c0001t0002g0180 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.400+6225A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145521238 | ||||||
chr4:145521510
|
C | T | 1 | a0001c0001t0001g0265 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.400+6497C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145521510 | ||||||
chr4:145521731
|
C | T | 2 | a0001c0001t0020g0077a0001c0001t0020g0153 | 2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.400+6718C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145521731 | ||||||
chr4:145521828
|
G | A | 4 | a0001c0001t0014g0039a0001c0001t0014g0066a0001c0001t0014g0067others(1): Show | 4 | HG02145.hp2 HG02451.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.400+6815G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145521828 | ||||||
chr4:145521900
|
T | TA | 17 | a0001c0001t0001g0009a0001c0001t0001g0094a0001c0001t0001g0156others(14): Show | 18 | HG01175.hp2 HG01433.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.400+6905dupA | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145521900 | |||||
chr4:145521900
|
TA | T | 69 | a0001c0001t0001g0052a0001c0001t0001g0078a0001c0001t0001g0093others(66): Show | 72 | HG00423.hp2 HG00621.hp1 HG01081.hp1 others(69): Show |
intron_variant | MODIFIER | c.400+6905delA | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145521900 | |||||
chr4:145521900
|
TAA | T | 8 | a0001c0001t0004g0231a0001c0001t0004g0232a0001c0001t0005g0021others(5): Show | 8 | HG00438.hp1 HG02135.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.400+6904_400+6905d others(4): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145521900 | |||||
chr4:145521946
|
C | G | 1 | a0001c0001t0014g0039 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.400+6933C>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145521946 | ||||||
chr4:145522094
|
T | TGAGGAGA others(4): Show |
8 | a0001c0001t0020g0077a0001c0001t0020g0153a0001c0002t0012g0050others(5): Show | 8 | HG01884.hp1 HG02109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.400+7083_400+7084i others(13): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145522094 | |||||
chr4:145522117
|
A | G | 4 | a0001c0001t0014g0039a0001c0001t0014g0066a0001c0001t0014g0067others(1): Show | 4 | HG02145.hp2 HG02451.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.400+7104A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145522117 | ||||||
chr4:145522248
|
G | A | 2 | a0001c0003t0012g0072a0001c0003t0012g0144 | 2 | HG01884.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.400+7235G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145522248 | ||||||
chr4:145522253
|
C | T | 2 | a0001c0001t0006g0120a0001c0001t0006g0225 | 2 | NA18973.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.400+7240C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145522253 | ||||||
chr4:145522298
|
C | CA | 12 | a0001c0001t0006g0118a0001c0001t0006g0119a0001c0001t0006g0120others(9): Show | 12 | HG00738.hp2 HG01081.hp2 HG03654.hp1 others(9): Show |
intron_variant | MODIFIER | c.400+7292dupA | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145522298 | |||||
chr4:145522319
|
G | C | 3 | a0001c0002t0012g0050a0001c0002t0012g0069a0001c0002t0012g0143 | 3 | HG02145.hp1 HG02257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.400+7306G>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145522319 | ||||||
chr4:145522361
|
G | A | 5 | a0001c0001t0009g0286a0001c0001t0017g0162a0001c0001t0017g0163others(2): Show | 5 | HG02055.hp2 HG02280.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.400+7348G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145522361 | ||||||
chr4:145522366
|
C | T | 2 | a0001c0001t0020g0077a0001c0001t0020g0153 | 2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.400+7353C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145522366 | ||||||
chr4:145522374
|
G | A | 5 | a0001c0001t0011g0040a0001c0001t0011g0041a0001c0001t0011g0073others(2): Show | 5 | HG02559.hp1 HG02647.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.400+7361G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145522374 | ||||||
chr4:145522464
|
G | A | 1 | a0001c0001t0002g0169 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.400+7451G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145522464 | ||||||
chr4:145522573
|
T | C | 1 | a0001c0001t0004g0116 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.400+7560T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145522573 | ||||||
chr4:145522654
|
GTGTTT | G | 5 | a0001c0001t0008g0016a0001c0001t0008g0051a0001c0001t0008g0155others(2): Show | 6 | HG01192.hp2 HG01496.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.400+7663_400+7667d others(7): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145522654 | |||||
chr4:145522684
|
G | GT | 6 | a0001c0001t0003g0258a0001c0001t0007g0005a0001c0001t0007g0019others(3): Show | 7 | HG01175.hp2 HG01261.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.400+7679dupT | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145522684 | |||||
chr4:145522886
|
C | T | 3 | a0001c0002t0012g0050a0001c0002t0012g0069a0001c0002t0012g0143 | 3 | HG02145.hp1 HG02257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.400+7873C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145522886 | ||||||
chr4:145522924
|
G | A | 3 | a0001c0001t0001g0058a0001c0001t0001g0101a0001c0001t0001g0209 | 3 | HG02451.hp2 HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.400+7911G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145522924 | ||||||
chr4:145522957
|
G | A | 3 | a0001c0002t0012g0050a0001c0002t0012g0069a0001c0002t0012g0143 | 3 | HG02145.hp1 HG02257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.400+7944G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145522957 | ||||||
chr4:145523214
|
T | C | 6 | a0001c0002t0012g0050a0001c0002t0012g0069a0001c0002t0012g0143others(3): Show | 6 | HG01884.hp1 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.400+8201T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145523214 | ||||||
chr4:145523279
|
G | A | 1 | a0001c0002t0033g0075 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.400+8266G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145523279 | ||||||
chr4:145523285
|
A | G | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG02135.hp1 HG04228.hp1 NA18945.hp1 others(1): Show |
intron_variant | MODIFIER | c.400+8272A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145523285 | ||||||
chr4:145523440
|
A | G | 1 | a0001c0001t0004g0080 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.400+8427A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145523440 | ||||||
chr4:145523483
|
A | G | 2 | a0001c0001t0010g0132a0001c0001t0010g0251 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.400+8470A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145523483 | ||||||
chr4:145523492
|
T | G | 5 | a0001c0001t0008g0016a0001c0001t0008g0051a0001c0001t0008g0155others(2): Show | 6 | HG01192.hp2 HG01496.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.400+8479T>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145523492 | ||||||
chr4:145523636
|
G | A | 2 | a0001c0001t0001g0272a0001c0001t0001g0278 | 2 | HG03704.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.400+8623G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145523636 | ||||||
chr4:145523732
|
G | A | 2 | a0001c0001t0001g0270a0001c0001t0001g0273 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.400+8719G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145523732 | ||||||
chr4:145523863
|
T | C | 1 | a0001c0001t0003g0255 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.400+8850T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145523863 | ||||||
chr4:145524067
|
GA | G | 3 | a0001c0002t0012g0050a0001c0002t0012g0069a0001c0002t0012g0143 | 3 | HG02145.hp1 HG02257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.400+9056delA | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145524067 | |||||
chr4:145524131
|
A | G | 1 | a0001c0002t0033g0075 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.400+9118A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145524131 | ||||||
chr4:145524143
|
C | G | 3 | a0001c0002t0012g0050a0001c0002t0012g0069a0001c0002t0012g0143 | 3 | HG02145.hp1 HG02257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.400+9130C>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145524143 | ||||||
chr4:145524372
|
T | C | 3 | a0001c0002t0012g0050a0001c0002t0012g0069a0001c0002t0012g0143 | 3 | HG02145.hp1 HG02257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.400+9359T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145524372 | ||||||
chr4:145524405
|
T | A | 3 | a0001c0001t0001g0052a0001c0001t0001g0078a0001c0001t0001g0165 | 3 | HG02109.hp1 HG02258.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.400+9392T>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145524405 | ||||||
chr4:145524528
|
T | C | 172 | a0001c0001t0001g0034a0001c0001t0001g0052a0001c0001t0001g0064others(169): Show | 182 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(179): Show |
intron_variant | MODIFIER | c.400+9515T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145524528 | ||||||
chr4:145524718
|
T | A | 4 | a0001c0001t0014g0039a0001c0001t0014g0066a0001c0001t0014g0067others(1): Show | 4 | HG02145.hp2 HG02451.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.400+9705T>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145524718 | ||||||
chr4:145524738
|
G | A | 1 | a0001c0001t0028g0033 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.400+9725G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145524738 | ||||||
chr4:145524790
|
GA | G | 285 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0017others(282): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.400+9790delA | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145524790 | |||||
chr4:145525236
|
A | G | 3 | a0001c0002t0012g0050a0001c0002t0012g0069a0001c0002t0012g0143 | 3 | HG02145.hp1 HG02257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.400+10223A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145525236 | ||||||
chr4:145525269
|
G | A | 8 | a0001c0001t0020g0077a0001c0001t0020g0153a0001c0002t0012g0050others(5): Show | 8 | HG01884.hp1 HG02109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.400+10256G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145525269 | ||||||
chr4:145525289
|
A | G | 3 | a0001c0001t0001g0034a0001c0001t0001g0064a0001c0001t0001g0065 | 3 | HG02622.hp1 HG03209.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.400+10276A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145525289 | ||||||
chr4:145525820
|
G | A | 1 | a0001c0002t0033g0075 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.400+10807G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145525820 | ||||||
chr4:145525952
|
T | C | 1 | a0001c0002t0033g0075 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.400+10939T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145525952 | ||||||
chr4:145526041
|
T | C | 107 | a0001c0001t0001g0034a0001c0001t0001g0052a0001c0001t0001g0064others(104): Show | 111 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(108): Show |
intron_variant | MODIFIER | c.400+11028T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145526041 | ||||||
chr4:145526077
|
A | T | 1 | a0001c0001t0001g0210 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.400+11064A>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145526077 | ||||||
chr4:145526450
|
A | G | 1 | a0001c0001t0014g0039 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.400+11437A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145526450 | ||||||
chr4:145526563
|
AGGACCCA others(1344): Show |
A | 5 | a0001c0001t0005g0020a0001c0001t0005g0021a0001c0001t0005g0043others(2): Show | 5 | HG00438.hp1 HG02135.hp2 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.400+11551_401-1189 others(4): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145526563 | ||||||
chr4:145526608
|
A | G | 3 | a0001c0001t0002g0267a0001c0001t0002g0269a0001c0001t0002g0277 | 3 | NA18979.hp1 NA18984.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.400+11595A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145526608 | ||||||
chr4:145526637
|
T | C | 86 | a0001c0001t0001g0052a0001c0001t0001g0078a0001c0001t0001g0093others(83): Show | 90 | HG00423.hp2 HG00621.hp1 HG01081.hp1 others(87): Show |
intron_variant | MODIFIER | c.400+11624T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145526637 | ||||||
chr4:145526856
|
A | C | 2 | a0001c0001t0002g0087a0001c0001t0002g0183 | 2 | HG00558.hp1 HG00597.hp1 |
intron_variant | MODIFIER | c.400+11843A>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145526856 | ||||||
chr4:145526872
|
C | T | 86 | a0001c0001t0001g0052a0001c0001t0001g0078a0001c0001t0001g0093others(83): Show | 90 | HG00423.hp2 HG00621.hp1 HG01081.hp1 others(87): Show |
intron_variant | MODIFIER | c.400+11859C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145526872 | ||||||
chr4:145527227
|
CT | C | 85 | a0001c0001t0001g0052a0001c0001t0001g0078a0001c0001t0001g0093others(82): Show | 89 | HG00423.hp2 HG00621.hp1 HG01081.hp1 others(86): Show |
intron_variant | MODIFIER | c.400+12228delT | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145527227 | |||||
chr4:145527254
|
T | C | 93 | a0001c0001t0001g0034a0001c0001t0001g0052a0001c0001t0001g0064others(90): Show | 97 | HG00423.hp2 HG00621.hp1 HG01081.hp1 others(94): Show |
intron_variant | MODIFIER | c.400+12241T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145527254 | ||||||
chr4:145527283
|
G | A | 2 | a0001c0001t0003g0135a0001c0001t0003g0258 | 2 | HG01175.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.400+12270G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145527283 | ||||||
chr4:145527292
|
C | T | 4 | a0001c0001t0014g0039a0001c0001t0014g0066a0001c0001t0014g0067others(1): Show | 4 | HG02145.hp2 HG02451.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.400+12279C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145527292 | ||||||
chr4:145527368
|
C | T | 2 | a0001c0001t0002g0096a0001c0001t0002g0198 | 2 | NA19002.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.400+12355C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145527368 | ||||||
chr4:145527425
|
G | A | 9 | a0001c0001t0001g0093a0001c0001t0001g0138a0001c0001t0001g0139others(6): Show | 10 | HG01081.hp1 HG01257.hp2 HG01928.hp2 others(7): Show |
intron_variant | MODIFIER | c.401-12379G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145527425 | ||||||
chr4:145527671
|
C | T | 5 | a0001c0001t0009g0286a0001c0001t0017g0162a0001c0001t0017g0163others(2): Show | 5 | HG02055.hp2 HG02280.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.401-12133C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145527671 | ||||||
chr4:145527767
|
T | A | 11 | a0001c0001t0005g0022a0001c0001t0005g0023a0001c0001t0005g0024others(8): Show | 11 | HG01243.hp2 HG01884.hp2 HG02040.hp1 others(8): Show |
intron_variant | MODIFIER | c.401-12037T>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145527767 | ||||||
chr4:145527863
|
AT | A | 51 | a0001c0001t0001g0052a0001c0001t0001g0078a0001c0001t0001g0093others(48): Show | 53 | HG00423.hp2 HG00621.hp1 HG01081.hp1 others(50): Show |
intron_variant | MODIFIER | c.401-11927delT | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145527863 | |||||
chr4:145527916
|
A | T | 5 | a0001c0001t0005g0020a0001c0001t0005g0021a0001c0001t0005g0043others(2): Show | 5 | HG00438.hp1 HG02135.hp2 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.401-11888A>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145527916 | ||||||
chr4:145527917
|
G | GA | 5 | a0001c0001t0005g0020a0001c0001t0005g0021a0001c0001t0005g0043others(2): Show | 5 | HG00438.hp1 HG02135.hp2 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.401-11887_401-1188 others(5): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145527917 | ||||||
chr4:145527962
|
G | A | 1 | a0001c0001t0001g0230 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.401-11842G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145527962 | ||||||
chr4:145528060
|
T | TAC | 22 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0192others(19): Show | 24 | HG00735.hp1 HG00738.hp2 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.401-11712_401-1171 others(6): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145528060 | |||||
chr4:145528060
|
T | TACAC | 4 | a0001c0001t0002g0086a0001c0001t0006g0224a0001c0001t0019g0219others(1): Show | 4 | HG00140.hp2 HG04204.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.401-11714_401-1171 others(8): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145528060 | |||||
chr4:145528060
|
TAC | T | 6 | a0001c0001t0020g0077a0001c0001t0020g0153a0001c0002t0012g0050others(3): Show | 6 | HG02145.hp1 HG02257.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.401-11712_401-1171 others(6): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145528060 | |||||
chr4:145528060
|
TACAC | T | 9 | a0001c0001t0001g0029a0001c0001t0001g0146a0001c0001t0004g0079others(6): Show | 10 | HG02572.hp2 HG02965.hp2 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.401-11714_401-1171 others(8): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145528060 | |||||
chr4:145528060
|
TACACAC | T | 50 | a0001c0001t0001g0052a0001c0001t0001g0078a0001c0001t0001g0093others(47): Show | 53 | HG00423.hp2 HG00621.hp1 HG01081.hp1 others(50): Show |
intron_variant | MODIFIER | c.401-11716_401-1171 others(10): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145528060 | |||||
chr4:145528060
|
TACACACA others(1): Show |
T | 25 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(22): Show | 26 | HG00438.hp2 HG01243.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.401-11718_401-1171 others(12): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145528060 | |||||
chr4:145528060
|
TACACACA others(5): Show |
T | 1 | a0001c0001t0007g0019 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.401-11722_401-1171 others(16): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145528060 | |||||
chr4:145528084
|
CACACACA others(3): Show |
C | 7 | a0001c0001t0005g0020a0001c0001t0005g0021a0001c0001t0005g0035others(4): Show | 7 | HG00438.hp1 HG02135.hp2 NA18964.hp2 others(4): Show |
intron_variant | MODIFIER | c.401-11708_401-1169 others(14): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145528084 | |||||
chr4:145528094
|
T | C | 1 | a0001c0001t0005g0046 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.401-11710T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145528094 | ||||||
chr4:145528107
|
AT | A | 6 | a0001c0001t0001g0216a0001c0001t0002g0166a0001c0001t0004g0231others(3): Show | 6 | HG01069.hp2 HG01070.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.401-11683delT | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145528107 | |||||
chr4:145528122
|
G | T | 29 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0054others(26): Show | 31 | HG00140.hp1 HG00544.hp1 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.401-11682G>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145528122 | ||||||
chr4:145528249
|
G | A | 3 | a0001c0001t0002g0089a0001c0001t0002g0175a0001c0001t0002g0196 | 3 | HG00544.hp2 NA18747.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.401-11555G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145528249 | ||||||
chr4:145528304
|
T | C | 1 | a0001c0001t0008g0155 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.401-11500T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145528304 | ||||||
chr4:145528394
|
C | T | 5 | a0001c0001t0011g0040a0001c0001t0011g0041a0001c0001t0011g0073others(2): Show | 5 | HG02559.hp1 HG02647.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.401-11410C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145528394 | ||||||
chr4:145528428
|
C | CG | 27 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(24): Show | 28 | HG00438.hp1 HG01243.hp1 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.401-11370dupG | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145528428 | |||||
chr4:145528949
|
G | A | 2 | a0001c0001t0020g0077a0001c0001t0020g0153 | 2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.401-10855G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145528949 | ||||||
chr4:145529305
|
G | A | 1 | a0001c0001t0001g0165 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.401-10499G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145529305 | ||||||
chr4:145529753
|
T | C | 3 | a0001c0001t0001g0018a0001c0001t0001g0270a0001c0001t0001g0273 | 4 | HG01516.hp1 HG01517.hp2 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.401-10051T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145529753 | ||||||
chr4:145529818
|
G | A | 51 | a0001c0001t0003g0003a0001c0001t0003g0004a0001c0001t0003g0014others(48): Show | 57 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.401-9986G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145529818 | ||||||
chr4:145529829
|
A | G | 2 | a0001c0003t0012g0072a0001c0003t0012g0144 | 2 | HG01884.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.401-9975A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145529829 | ||||||
chr4:145529875
|
G | A | 2 | a0001c0001t0010g0132a0001c0001t0010g0251 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.401-9929G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145529875 | ||||||
chr4:145529895
|
T | A | 1 | a0001c0001t0001g0188 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.401-9909T>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145529895 | ||||||
chr4:145529907
|
T | C | 2 | a0001c0001t0011g0040a0001c0001t0011g0041 | 2 | HG02559.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.401-9897T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145529907 | ||||||
chr4:145529979
|
A | C | 2 | a0001c0001t0021g0027a0001c0001t0021g0028 | 2 | HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.401-9825A>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145529979 | ||||||
chr4:145530075
|
G | A | 4 | a0001c0001t0004g0006a0001c0001t0004g0109a0001c0001t0004g0110others(1): Show | 5 | HG00423.hp2 HG02132.hp2 NA18945.hp2 others(2): Show |
intron_variant | MODIFIER | c.401-9729G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145530075 | ||||||
chr4:145530604
|
A | C | 98 | a0001c0001t0001g0034a0001c0001t0001g0052a0001c0001t0001g0064others(95): Show | 102 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(99): Show |
intron_variant | MODIFIER | c.401-9200A>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145530604 | ||||||
chr4:145530628
|
C | A | 94 | a0001c0001t0001g0034a0001c0001t0001g0052a0001c0001t0001g0064others(91): Show | 98 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.401-9176C>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145530628 | ||||||
chr4:145530705
|
A | AAAACTAT others(315): Show |
2 | a0001c0003t0012g0072a0001c0003t0012g0144 | 2 | HG01884.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.401-9082_401-9081i others(324): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145530705 | |||||
chr4:145531056
|
C | T | 1 | a0001c0001t0009g0286 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.401-8748C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145531056 | ||||||
chr4:145531245
|
G | A | 1 | a0001c0002t0012g0050 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.401-8559G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145531245 | ||||||
chr4:145531364
|
C | T | 1 | a0001c0001t0002g0180 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.401-8440C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145531364 | ||||||
chr4:145531399
|
C | G | 1 | a0001c0001t0007g0019 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.401-8405C>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145531399 | ||||||
chr4:145531621
|
T | C | 90 | a0001c0001t0001g0034a0001c0001t0001g0052a0001c0001t0001g0064others(87): Show | 94 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(91): Show |
intron_variant | MODIFIER | c.401-8183T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145531621 | ||||||
chr4:145531715
|
A | C | 1 | a0001c0002t0012g0069 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.401-8089A>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145531715 | ||||||
chr4:145531958
|
G | A | 27 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(24): Show | 28 | HG00438.hp1 HG01243.hp1 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.401-7846G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145531958 | ||||||
chr4:145532147
|
A | G | 3 | a0001c0001t0002g0095a0001c0001t0002g0181a0001c0001t0002g0194 | 3 | HG00099.hp2 HG01099.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.401-7657A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145532147 | ||||||
chr4:145532274
|
C | T | 27 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(24): Show | 28 | HG00438.hp1 HG01243.hp1 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.401-7530C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145532274 | ||||||
chr4:145532428
|
G | A | 1 | a0001c0001t0028g0033 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.401-7376G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145532428 | ||||||
chr4:145532428
|
G | GT | 4 | a0001c0001t0001g0107a0001c0001t0001g0215a0001c0001t0001g0216others(1): Show | 4 | HG01070.hp1 HG01071.hp1 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.401-7370dupT | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145532428 | |||||
chr4:145532503
|
A | T | 1 | a0001c0001t0001g0158 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.401-7301A>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145532503 | ||||||
chr4:145532521
|
T | C | 1 | a0001c0001t0001g0187 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.401-7283T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145532521 | ||||||
chr4:145532731
|
C | T | 16 | a0001c0001t0005g0020a0001c0001t0005g0021a0001c0001t0005g0022others(13): Show | 16 | HG00438.hp1 HG01243.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.401-7073C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145532731 | ||||||
chr4:145532769
|
G | A | 45 | a0001c0001t0001g0052a0001c0001t0001g0078a0001c0001t0001g0093others(42): Show | 47 | HG00423.hp2 HG00621.hp1 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.401-7035G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145532769 | ||||||
chr4:145532775
|
T | C | 1 | a0001c0002t0033g0075 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.401-7029T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145532775 | ||||||
chr4:145532777
|
G | C | 4 | a0001c0001t0014g0039a0001c0001t0014g0066a0001c0001t0014g0067others(1): Show | 4 | HG02145.hp2 HG02451.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.401-7027G>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145532777 | ||||||
chr4:145532963
|
T | A | 1 | a0001c0001t0001g0193 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.401-6841T>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145532963 | ||||||
chr4:145533196
|
AG | A | 13 | a0001c0001t0006g0118a0001c0001t0006g0119a0001c0001t0006g0120others(10): Show | 13 | HG00738.hp2 HG01081.hp2 HG03654.hp1 others(10): Show |
intron_variant | MODIFIER | c.401-6605delG | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145533196 | |||||
chr4:145533253
|
G | A | 1 | a0001c0001t0006g0218 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.401-6551G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145533253 | ||||||
chr4:145533293
|
G | C | 2 | a0001c0001t0022g0057a0001c0001t0022g0217 | 2 | HG02723.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.401-6511G>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145533293 | ||||||
chr4:145533477
|
G | C | 2 | a0001c0001t0020g0077a0001c0001t0020g0153 | 2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.401-6327G>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145533477 | ||||||
chr4:145533535
|
T | C | 49 | a0001c0001t0003g0003a0001c0001t0003g0004a0001c0001t0003g0014others(46): Show | 54 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.401-6269T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145533535 | ||||||
chr4:145533598
|
C | T | 5 | a0001c0001t0011g0040a0001c0001t0011g0041a0001c0001t0011g0073others(2): Show | 5 | HG02559.hp1 HG02647.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.401-6206C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145533598 | ||||||
chr4:145533928
|
C | T | 2 | a0001c0001t0020g0077a0001c0001t0020g0153 | 2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.401-5876C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145533928 | ||||||
chr4:145534377
|
G | A | 1 | a0001c0001t0002g0086 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.401-5427G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145534377 | ||||||
chr4:145534505
|
C | G | 4 | a0001c0001t0017g0162a0001c0001t0017g0163a0001c0001t0017g0164others(1): Show | 4 | HG02055.hp2 HG02280.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.401-5299C>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145534505 | ||||||
chr4:145534513
|
T | A | 1 | a0001c0001t0001g0103 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.401-5291T>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145534513 | ||||||
chr4:145534660
|
C | T | 2 | a0001c0003t0012g0072a0001c0003t0012g0144 | 2 | HG01884.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.401-5144C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145534660 | ||||||
chr4:145534684
|
T | C | 6 | a0001c0001t0001g0122a0001c0001t0001g0228a0001c0001t0001g0229others(3): Show | 6 | HG01891.hp1 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.401-5120T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145534684 | ||||||
chr4:145534866
|
G | A | 1 | a0001c0001t0016g0091 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.401-4938G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145534866 | ||||||
chr4:145535037
|
A | G | 173 | a0001c0001t0001g0034a0001c0001t0001g0052a0001c0001t0001g0064others(170): Show | 183 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.401-4767A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145535037 | ||||||
chr4:145535392
|
C | T | 1 | a0001c0001t0002g0214 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.401-4412C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145535392 | ||||||
chr4:145535536
|
G | C | 1 | a0001c0001t0030g0142 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.401-4268G>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145535536 | ||||||
chr4:145535600
|
G | A | 1 | a0001c0003t0012g0072 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.401-4204G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145535600 | ||||||
chr4:145535832
|
C | T | 3 | a0001c0001t0001g0056a0001c0001t0003g0092a0001c0001t0016g0091 | 3 | HG00609.hp2 HG02040.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.401-3972C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145535832 | ||||||
chr4:145535967
|
C | G | 2 | a0001c0001t0006g0118a0001c0001t0006g0119 | 2 | NA18975.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.401-3837C>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145535967 | ||||||
chr4:145535984
|
C | CA | 12 | a0001c0001t0003g0135a0001c0001t0003g0250a0001c0001t0003g0258others(9): Show | 12 | HG01167.hp2 HG01169.hp2 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.401-3804dupA | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 145535984 | |||||
chr4:145536149
|
G | A | 1 | a0001c0001t0026g0213 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.401-3655G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145536149 | ||||||
chr4:145536226
|
T | C | 5 | a0001c0001t0008g0016a0001c0001t0008g0051a0001c0001t0008g0155others(2): Show | 6 | HG01192.hp2 HG01496.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.401-3578T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145536226 | ||||||
chr4:145536234
|
C | T | 5 | a0001c0001t0009g0286a0001c0001t0017g0162a0001c0001t0017g0163others(2): Show | 5 | HG02055.hp2 HG02280.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.401-3570C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145536234 | ||||||
chr4:145536246
|
G | C | 2 | a0001c0001t0003g0129a0001c0001t0003g0244 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.401-3558G>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145536246 | ||||||
chr4:145536259
|
A | G | 1 | a0001c0001t0002g0099 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.401-3545A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145536259 | ||||||
chr4:145536530
|
C | A | 1 | a0001c0001t0001g0177 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.401-3274C>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145536530 | ||||||
chr4:145537032
|
G | A | 1 | a0001c0001t0002g0098 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.401-2772G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145537032 | ||||||
chr4:145537393
|
G | C | 1 | a0001c0001t0004g0115 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.401-2411G>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145537393 | ||||||
chr4:145537570
|
G | T | 2 | a0001c0001t0020g0077a0001c0001t0020g0153 | 2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.401-2234G>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145537570 | ||||||
chr4:145537643
|
T | C | 1 | a0001c0001t0004g0053 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.401-2161T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145537643 | ||||||
chr4:145537962
|
G | A | 1 | a0001c0001t0014g0039 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.401-1842G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145537962 | ||||||
chr4:145537962
|
G | T | 13 | a0001c0001t0005g0023a0001c0001t0005g0024a0001c0001t0005g0025others(10): Show | 14 | HG01192.hp2 HG01496.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.401-1842G>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145537962 | ||||||
chr4:145538023
|
G | A | 2 | a0001c0001t0001g0055a0001c0001t0001g0094 | 2 | NA18941.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.401-1781G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145538023 | ||||||
chr4:145538072
|
A | G | 2 | a0001c0001t0020g0077a0001c0001t0020g0153 | 2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.401-1732A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145538072 | ||||||
chr4:145538107
|
C | T | 1 | a0001c0001t0002g0199 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.401-1697C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145538107 | ||||||
chr4:145538136
|
T | C | 53 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0004g0151others(50): Show | 55 | HG00438.hp1 HG01192.hp2 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.401-1668T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145538136 | ||||||
chr4:145538747
|
G | T | 23 | a0001c0001t0005g0020a0001c0001t0005g0021a0001c0001t0005g0022others(20): Show | 24 | HG00438.hp1 HG01243.hp2 HG01261.hp1 others(21): Show |
intron_variant | MODIFIER | c.401-1057G>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145538747 | ||||||
chr4:145538901
|
C | T | 39 | a0001c0001t0005g0020a0001c0001t0005g0021a0001c0001t0005g0022others(36): Show | 41 | HG00438.hp1 HG01192.hp2 HG01243.hp2 others(38): Show |
intron_variant | MODIFIER | c.401-903C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145538901 | ||||||
chr4:145539057
|
C | T | 7 | a0001c0001t0008g0016a0001c0001t0008g0051a0001c0001t0008g0155others(4): Show | 8 | HG01070.hp2 HG01192.hp2 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.401-747C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145539057 | ||||||
chr4:145539188
|
G | A | 2 | a0001c0001t0020g0077a0001c0001t0020g0153 | 2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.401-616G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145539188 | ||||||
chr4:145539403
|
C | T | 28 | a0001c0001t0001g0093a0001c0001t0001g0138a0001c0001t0001g0139others(25): Show | 30 | HG00423.hp2 HG00621.hp1 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.401-401C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145539403 | ||||||
chr4:145539488
|
T | G | 1 | a0001c0001t0001g0177 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.401-316T>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 2/6 | chr4 | 145539488 | ||||||
chr4:145540197
|
G | A | 1 | a0001c0001t0026g0213 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.658+136G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 3/6 | chr4 | 145540197 | ||||||
chr4:145540284
|
A | G | 2 | a0001c0001t0003g0134a0001c0001t0003g0256 | 2 | HG01516.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.658+223A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 3/6 | chr4 | 145540284 | ||||||
chr4:145540382
|
C | T | 90 | a0001c0001t0001g0093a0001c0001t0001g0122a0001c0001t0001g0138others(87): Show | 94 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(91): Show |
intron_variant | MODIFIER | c.658+321C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 3/6 | chr4 | 145540382 | ||||||
chr4:145540462
|
G | A | 1 | a0001c0001t0004g0104 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.658+401G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 3/6 | chr4 | 145540462 | ||||||
chr4:145540538
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.658+477C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 3/6 | chr4 | 145540538 | ||||||
chr4:145540548
|
G | A | 2 | a0001c0001t0020g0077a0001c0001t0020g0153 | 2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.658+487G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 3/6 | chr4 | 145540548 | ||||||
chr4:145540627
|
A | G | 1 | a0001c0001t0009g0286 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.658+566A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 3/6 | chr4 | 145540627 | ||||||
chr4:145540900
|
A | T | 1 | a0001c0001t0001g0029 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.658+839A>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 3/6 | chr4 | 145540900 | ||||||
chr4:145541339
|
T | TAGTATCA others(184): Show |
1 | a0001c0001t0008g0262 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.659-1180_659-1179i others(193): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr4 | 145541339 | |||||
chr4:145541403
|
C | T | 5 | a0001c0001t0008g0016a0001c0001t0008g0051a0001c0001t0008g0155others(2): Show | 6 | HG01192.hp2 HG01496.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.659-1179C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 3/6 | chr4 | 145541403 | ||||||
chr4:145541481
|
C | A | 1 | a0001c0001t0001g0188 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.659-1101C>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 3/6 | chr4 | 145541481 | ||||||
chr4:145541481
|
C | T | 1 | a0001c0001t0001g0161 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.659-1101C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 3/6 | chr4 | 145541481 | ||||||
chr4:145541482
|
G | A | 1 | a0001c0001t0004g0149 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.659-1100G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 3/6 | chr4 | 145541482 | ||||||
chr4:145541728
|
T | G | 4 | a0001c0001t0017g0162a0001c0001t0017g0163a0001c0001t0017g0164others(1): Show | 4 | HG02055.hp2 HG02280.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.659-854T>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 3/6 | chr4 | 145541728 | ||||||
chr4:145541787
|
T | C | 2 | a0001c0001t0003g0131a0001c0001t0003g0282 | 2 | HG00639.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.659-795T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 3/6 | chr4 | 145541787 | ||||||
chr4:145541993
|
T | C | 125 | a0001c0001t0001g0034a0001c0001t0001g0064a0001c0001t0001g0065others(122): Show | 133 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.659-589T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 3/6 | chr4 | 145541993 | ||||||
chr4:145542118
|
T | C | 2 | a0001c0001t0007g0030a0001c0001t0007g0154 | 2 | HG01261.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.659-464T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 3/6 | chr4 | 145542118 | ||||||
chr4:145542285
|
A | G | 1 | a0001c0001t0014g0039 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.659-297A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 3/6 | chr4 | 145542285 | ||||||
chr4:145542293
|
G | T | 1 | a0001c0001t0004g0207 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.659-289G>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 3/6 | chr4 | 145542293 | ||||||
chr4:145542374
|
A | C | 4 | a0001c0001t0014g0039a0001c0001t0014g0066a0001c0001t0014g0067others(1): Show | 4 | HG02145.hp2 HG02451.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.659-208A>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 3/6 | chr4 | 145542374 | ||||||
chr4:145542398
|
T | C | 16 | a0001c0001t0005g0020a0001c0001t0005g0021a0001c0001t0005g0022others(13): Show | 16 | HG00438.hp1 HG01243.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.659-184T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 3/6 | chr4 | 145542398 | ||||||
chr4:145542552
|
T | C | 1 | a0001c0001t0026g0213 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.659-30T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 3/6 | chr4 | 145542552 | ||||||
chr4:145542814
|
T | C | 171 | a0001c0001t0001g0034a0001c0001t0001g0064a0001c0001t0001g0065others(168): Show | 181 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(178): Show |
intron_variant | MODIFIER | c.775+116T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | chr4 | 145542814 | ||||||
chr4:145542851
|
A | G | 2 | a0001c0001t0020g0077a0001c0001t0020g0153 | 2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.775+153A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | chr4 | 145542851 | ||||||
chr4:145543127
|
C | T | 2 | a0001c0003t0012g0072a0001c0003t0012g0144 | 2 | HG01884.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.775+429C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | chr4 | 145543127 | ||||||
chr4:145543274
|
G | T | 1 | a0001c0001t0009g0286 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.775+576G>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | chr4 | 145543274 | ||||||
chr4:145543321
|
G | A | 1 | a0001c0001t0005g0047 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.775+623G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | chr4 | 145543321 | ||||||
chr4:145543353
|
A | G | 4 | a0001c0001t0014g0039a0001c0001t0014g0066a0001c0001t0014g0067others(1): Show | 4 | HG02145.hp2 HG02451.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.775+655A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | chr4 | 145543353 | ||||||
chr4:145543545
|
C | CAGCCTGA others(8): Show |
1 | a0001c0001t0002g0170 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.775+848_775+862dup others(15): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr4 | 145543545 | |||||
chr4:145543576
|
A | C | 3 | a0001c0001t0005g0023a0001c0001t0005g0024a0001c0001t0005g0045 | 3 | HG01884.hp2 HG03130.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.775+878A>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | chr4 | 145543576 | ||||||
chr4:145543621
|
C | T | 74 | a0001c0001t0003g0003a0001c0001t0003g0004a0001c0001t0003g0014others(71): Show | 80 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.775+923C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | chr4 | 145543621 | ||||||
chr4:145543928
|
C | T | 2 | a0001c0001t0022g0057a0001c0001t0022g0217 | 2 | HG02723.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.775+1230C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | chr4 | 145543928 | ||||||
chr4:145543942
|
T | C | 86 | a0001c0001t0001g0034a0001c0001t0001g0064a0001c0001t0001g0065others(83): Show | 90 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(87): Show |
intron_variant | MODIFIER | c.775+1244T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | chr4 | 145543942 | ||||||
chr4:145544191
|
AG | A | 3 | a0001c0002t0012g0050a0001c0002t0012g0069a0001c0002t0012g0143 | 3 | HG02145.hp1 HG02257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.775+1495delG | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr4 | 145544191 | |||||
chr4:145544195
|
A | G | 1 | a0001c0001t0002g0170 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.775+1497A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | chr4 | 145544195 | ||||||
chr4:145544197
|
G | C | 1 | a0001c0001t0002g0170 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.775+1499G>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | chr4 | 145544197 | ||||||
chr4:145544213
|
C | T | 2 | a0001c0001t0010g0132a0001c0001t0010g0251 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.775+1515C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | chr4 | 145544213 | ||||||
chr4:145544227
|
CTCTG | C | 4 | a0001c0001t0014g0039a0001c0001t0014g0066a0001c0001t0014g0067others(1): Show | 4 | HG02145.hp2 HG02451.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.775+1533_775+1536d others(6): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr4 | 145544227 | |||||
chr4:145544253
|
G | A | 2 | a0001c0001t0020g0077a0001c0001t0020g0153 | 2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.775+1555G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | chr4 | 145544253 | ||||||
chr4:145544287
|
C | T | 90 | a0001c0001t0001g0093a0001c0001t0001g0122a0001c0001t0001g0138others(87): Show | 94 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(91): Show |
intron_variant | MODIFIER | c.775+1589C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | chr4 | 145544287 | ||||||
chr4:145544458
|
G | T | 1 | a0001c0001t0002g0170 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.775+1760G>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | chr4 | 145544458 | ||||||
chr4:145544581
|
C | CA | 5 | a0001c0001t0007g0005a0001c0001t0007g0030a0001c0001t0007g0031others(2): Show | 6 | HG01261.hp1 HG02630.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.775+1895dupA | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr4 | 145544581 | |||||
chr4:145544661
|
A | G | 1 | a0001c0001t0004g0105 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.775+1963A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | chr4 | 145544661 | ||||||
chr4:145544924
|
G | A | 1 | a0001c0001t0002g0170 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.776-1779G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | chr4 | 145544924 | ||||||
chr4:145544925
|
A | G | 1 | a0001c0001t0002g0170 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.776-1778A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | chr4 | 145544925 | ||||||
chr4:145545082
|
G | A | 4 | a0001c0001t0017g0162a0001c0001t0017g0163a0001c0001t0017g0164others(1): Show | 4 | HG02055.hp2 HG02280.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.776-1621G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | chr4 | 145545082 | ||||||
chr4:145545217
|
G | A | 4 | a0001c0001t0001g0107a0001c0001t0001g0208a0001c0001t0001g0215others(1): Show | 4 | HG01070.hp1 HG01071.hp1 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.776-1486G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | chr4 | 145545217 | ||||||
chr4:145545220
|
A | C | 1 | a0001c0001t0001g0070 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.776-1483A>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | chr4 | 145545220 | ||||||
chr4:145545274
|
C | G | 1 | a0001c0001t0004g0060 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.776-1429C>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | chr4 | 145545274 | ||||||
chr4:145545311
|
T | C | 1 | a0001c0001t0002g0202 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.776-1392T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | chr4 | 145545311 | ||||||
chr4:145545313
|
G | A | 1 | a0001c0001t0002g0202 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.776-1390G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | chr4 | 145545313 | ||||||
chr4:145545453
|
T | A | 2 | a0001c0003t0012g0072a0001c0003t0012g0144 | 2 | HG01884.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.776-1250T>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | chr4 | 145545453 | ||||||
chr4:145545521
|
T | C | 5 | a0001c0001t0007g0005a0001c0001t0007g0030a0001c0001t0007g0031others(2): Show | 6 | HG01261.hp1 HG02630.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.776-1182T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | chr4 | 145545521 | ||||||
chr4:145545537
|
A | G | 1 | a0001c0001t0002g0175 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.776-1166A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | chr4 | 145545537 | ||||||
chr4:145545549
|
G | GT | 158 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0017others(155): Show | 171 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(168): Show |
intron_variant | MODIFIER | c.776-1144dupT | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr4 | 145545549 | |||||
chr4:145545549
|
G | GTT | 9 | a0001c0001t0001g0034a0001c0001t0001g0064a0001c0001t0001g0065others(6): Show | 9 | HG02055.hp2 HG02280.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.776-1145_776-1144d others(4): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr4 | 145545549 | |||||
chr4:145545556
|
T | G | 4 | a0001c0001t0003g0247a0001c0001t0020g0077a0001c0001t0020g0153others(1): Show | 4 | HG01070.hp2 HG02602.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.776-1147T>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | chr4 | 145545556 | ||||||
chr4:145545556
|
T | TG | 8 | a0001c0001t0005g0022a0001c0001t0005g0023a0001c0001t0008g0016others(5): Show | 9 | HG01192.hp2 HG01243.hp2 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.776-1147_776-1146i others(3): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | chr4 | 145545556 | ||||||
chr4:145545556
|
T | TGTG | 13 | a0001c0001t0005g0020a0001c0001t0005g0021a0001c0001t0005g0025others(10): Show | 13 | HG00438.hp1 HG02040.hp1 HG02132.hp1 others(10): Show |
intron_variant | MODIFIER | c.776-1147_776-1146i others(5): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | chr4 | 145545556 | ||||||
chr4:145545556
|
T | TTG | 45 | a0001c0001t0003g0003a0001c0001t0003g0004a0001c0001t0003g0014others(42): Show | 51 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.776-1146_776-1145i others(4): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr4 | 145545556 | |||||
chr4:145545556
|
T | TTGTG | 12 | a0001c0001t0006g0118a0001c0001t0006g0119a0001c0001t0006g0120others(9): Show | 12 | HG00738.hp2 HG01081.hp2 HG03927.hp1 others(9): Show |
intron_variant | MODIFIER | c.776-1146_776-1145i others(6): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr4 | 145545556 | |||||
chr4:145545558
|
T | G | 84 | a0001c0001t0003g0003a0001c0001t0003g0004a0001c0001t0003g0014others(81): Show | 91 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.776-1145T>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | chr4 | 145545558 | ||||||
chr4:145545558
|
T | TG | 11 | a0001c0001t0001g0249a0001c0001t0001g0265a0001c0001t0002g0170others(8): Show | 11 | HG00140.hp1 HG01884.hp2 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.776-1145_776-1144i others(3): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | chr4 | 145545558 | ||||||
chr4:145545558
|
T | TGTG | 10 | a0001c0001t0007g0005a0001c0001t0007g0019a0001c0001t0007g0030others(7): Show | 11 | HG01261.hp1 HG01884.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.776-1145_776-1144i others(5): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | chr4 | 145545558 | ||||||
chr4:145545558
|
T | TTG | 11 | a0001c0001t0003g0240a0001c0001t0003g0254a0001c0001t0011g0040others(8): Show | 11 | HG00609.hp1 HG02145.hp1 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.776-1125_776-1124d others(4): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr4 | 145545558 | |||||
chr4:145545560
|
G | T | 53 | a0001c0001t0001g0093a0001c0001t0001g0103a0001c0001t0001g0122others(50): Show | 55 | HG00423.hp2 HG00621.hp1 HG01081.hp1 others(52): Show |
intron_variant | MODIFIER | c.776-1143G>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | chr4 | 145545560 | ||||||
chr4:145545625
|
A | C | 13 | a0001c0001t0006g0118a0001c0001t0006g0119a0001c0001t0006g0120others(10): Show | 13 | HG00738.hp2 HG01081.hp2 HG03654.hp1 others(10): Show |
intron_variant | MODIFIER | c.776-1078A>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | chr4 | 145545625 | ||||||
chr4:145545723
|
C | T | 90 | a0001c0001t0001g0093a0001c0001t0001g0122a0001c0001t0001g0138others(87): Show | 94 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(91): Show |
intron_variant | MODIFIER | c.776-980C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | chr4 | 145545723 | ||||||
chr4:145545976
|
G | T | 1 | a0001c0001t0002g0170 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.776-727G>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | chr4 | 145545976 | ||||||
chr4:145546046
|
G | A | 2 | a0001c0001t0001g0100a0001c0001t0001g0205 | 2 | HG02809.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.776-657G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | chr4 | 145546046 | ||||||
chr4:145546274
|
A | G | 90 | a0001c0001t0001g0093a0001c0001t0001g0122a0001c0001t0001g0138others(87): Show | 94 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(91): Show |
intron_variant | MODIFIER | c.776-429A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 4/6 | chr4 | 145546274 | ||||||
chr4:145547179
|
G | C | 4 | a0001c0001t0020g0077a0001c0001t0020g0153a0001c0001t0021g0027others(1): Show | 4 | HG02895.hp1 HG02976.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.997+255G>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145547179 | ||||||
chr4:145547291
|
CAGTAAAT | C | 85 | a0001c0001t0001g0093a0001c0001t0001g0122a0001c0001t0001g0138others(82): Show | 89 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.997+370_997+376del others(7): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr4 | 145547291 | |||||
chr4:145547469
|
A | G | 1 | a0001c0001t0011g0074 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.997+545A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145547469 | ||||||
chr4:145547741
|
G | C | 7 | a0001c0001t0005g0042a0001c0001t0007g0005a0001c0001t0007g0019others(4): Show | 8 | HG01261.hp1 HG02630.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.997+817G>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145547741 | ||||||
chr4:145547783
|
T | C | 1 | a0001c0001t0023g0128 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.997+859T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145547783 | ||||||
chr4:145547888
|
G | A | 4 | a0001c0001t0017g0162a0001c0001t0017g0163a0001c0001t0017g0164others(1): Show | 4 | HG02055.hp2 HG02280.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.997+964G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145547888 | ||||||
chr4:145547896
|
T | G | 1 | a0001c0001t0005g0045 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.997+972T>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145547896 | ||||||
chr4:145547901
|
C | CT | 74 | a0001c0001t0003g0003a0001c0001t0003g0004a0001c0001t0003g0014others(71): Show | 80 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.997+978dupT | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr4 | 145547901 | |||||
chr4:145547940
|
T | A | 1 | a0001c0002t0033g0075 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.997+1016T>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145547940 | ||||||
chr4:145548129
|
T | A | 3 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0274 | 3 | HG02027.hp1 HG02155.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.997+1205T>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145548129 | ||||||
chr4:145548202
|
TTTTA | T | 4 | a0001c0001t0020g0077a0001c0001t0020g0153a0001c0001t0021g0027others(1): Show | 4 | HG02895.hp1 HG02976.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.997+1304_997+1307d others(6): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr4 | 145548202 | |||||
chr4:145548705
|
A | G | 8 | a0001c0001t0013g0036a0001c0001t0013g0037a0001c0001t0013g0038others(5): Show | 8 | HG02735.hp1 HG03017.hp2 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.997+1781A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145548705 | ||||||
chr4:145548786
|
G | A | 168 | a0001c0001t0001g0093a0001c0001t0001g0122a0001c0001t0001g0138others(165): Show | 178 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(175): Show |
intron_variant | MODIFIER | c.997+1862G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145548786 | ||||||
chr4:145548834
|
G | A | 2 | a0001c0001t0020g0077a0001c0001t0020g0153 | 2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.997+1910G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145548834 | ||||||
chr4:145548890
|
A | T | 1 | a0001c0001t0002g0173 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.997+1966A>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145548890 | ||||||
chr4:145548907
|
C | G | 1 | a0001c0001t0002g0186 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.997+1983C>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145548907 | ||||||
chr4:145549047
|
AC | A | 5 | a0001c0001t0008g0016a0001c0001t0008g0051a0001c0001t0008g0155others(2): Show | 6 | HG01192.hp2 HG01496.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.997+2124delC | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145549047 | ||||||
chr4:145549150
|
A | G | 1 | a0001c0001t0001g0209 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.997+2226A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145549150 | ||||||
chr4:145549312
|
T | C | 4 | a0001c0001t0014g0039a0001c0001t0014g0066a0001c0001t0014g0067others(1): Show | 4 | HG02145.hp2 HG02451.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.997+2388T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145549312 | ||||||
chr4:145549433
|
G | A | 4 | a0001c0001t0001g0122a0001c0001t0001g0228a0001c0001t0001g0229others(1): Show | 4 | HG01891.hp1 HG03041.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.997+2509G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145549433 | ||||||
chr4:145549458
|
GAC | G | 3 | a0001c0001t0001g0011a0001c0001t0001g0102a0001c0001t0001g0210 | 4 | HG02486.hp1 HG02622.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.997+2542_997+2543d others(4): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr4 | 145549458 | |||||
chr4:145549867
|
A | G | 1 | a0001c0001t0002g0185 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.997+2943A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145549867 | ||||||
chr4:145550089
|
CTTAGT | C | 4 | a0001c0001t0015g0076a0001c0001t0015g0147a0001c0001t0015g0148others(1): Show | 4 | HG03453.hp1 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.997+3166_997+3170d others(7): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145550089 | ||||||
chr4:145550159
|
A | G | 2 | a0001c0001t0021g0027a0001c0001t0021g0028 | 2 | HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.997+3235A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145550159 | ||||||
chr4:145550283
|
C | T | 2 | a0001c0001t0021g0027a0001c0001t0021g0028 | 2 | HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.997+3359C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145550283 | ||||||
chr4:145550597
|
A | G | 1 | a0001c0001t0001g0230 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.998-3187A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145550597 | ||||||
chr4:145550785
|
T | C | 13 | a0001c0001t0006g0118a0001c0001t0006g0119a0001c0001t0006g0120others(10): Show | 13 | HG00738.hp2 HG01081.hp2 HG03654.hp1 others(10): Show |
intron_variant | MODIFIER | c.998-2999T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145550785 | ||||||
chr4:145550889
|
T | C | 23 | a0001c0001t0005g0020a0001c0001t0005g0021a0001c0001t0005g0022others(20): Show | 24 | HG00438.hp1 HG01243.hp2 HG01261.hp1 others(21): Show |
intron_variant | MODIFIER | c.998-2895T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145550889 | ||||||
chr4:145550967
|
T | G | 1 | a0001c0001t0001g0178 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.998-2817T>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145550967 | ||||||
chr4:145551240
|
C | T | 1 | a0001c0001t0005g0026 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.998-2544C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145551240 | ||||||
chr4:145551330
|
A | G | 1 | a0001c0001t0001g0275 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.998-2454A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145551330 | ||||||
chr4:145551526
|
G | C | 1 | a0001c0001t0002g0012 | 2 | HG01981.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.998-2258G>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145551526 | ||||||
chr4:145551684
|
A | G | 6 | a0001c0001t0007g0005a0001c0001t0007g0019a0001c0001t0007g0030others(3): Show | 7 | HG01261.hp1 HG02630.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.998-2100A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145551684 | ||||||
chr4:145551738
|
T | C | 1 | a0001c0001t0002g0086 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.998-2046T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145551738 | ||||||
chr4:145551997
|
A | G | 1 | a0001c0001t0018g0252 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.998-1787A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145551997 | ||||||
chr4:145552184
|
T | C | 1 | a0001c0001t0002g0182 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.998-1600T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145552184 | ||||||
chr4:145552189
|
T | G | 1 | a0001c0001t0002g0182 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.998-1595T>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145552189 | ||||||
chr4:145552297
|
G | A | 27 | a0001c0001t0005g0020a0001c0001t0005g0021a0001c0001t0005g0022others(24): Show | 28 | HG00438.hp1 HG01243.hp2 HG01261.hp1 others(25): Show |
intron_variant | MODIFIER | c.998-1487G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145552297 | ||||||
chr4:145552302
|
G | A | 1 | a0001c0001t0001g0103 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.998-1482G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145552302 | ||||||
chr4:145552502
|
T | C | 23 | a0001c0001t0005g0020a0001c0001t0005g0021a0001c0001t0005g0022others(20): Show | 24 | HG00438.hp1 HG01243.hp2 HG01261.hp1 others(21): Show |
intron_variant | MODIFIER | c.998-1282T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145552502 | ||||||
chr4:145552512
|
G | T | 1 | a0001c0001t0007g0154 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.998-1272G>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145552512 | ||||||
chr4:145552583
|
G | A | 1 | a0001c0001t0004g0285 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.998-1201G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145552583 | ||||||
chr4:145552605
|
C | A | 1 | a0001c0001t0003g0237 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.998-1179C>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145552605 | ||||||
chr4:145552669
|
G | A | 1 | a0001c0001t0003g0134 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.998-1115G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145552669 | ||||||
chr4:145552798
|
C | A | 1 | a0001c0001t0032g0112 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.998-986C>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145552798 | ||||||
chr4:145552843
|
A | G | 92 | a0001c0001t0001g0093a0001c0001t0001g0122a0001c0001t0001g0138others(89): Show | 96 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(93): Show |
intron_variant | MODIFIER | c.998-941A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145552843 | ||||||
chr4:145552866
|
A | G | 2 | a0001c0001t0002g0098a0001c0001t0002g0201 | 2 | NA18944.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.998-918A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145552866 | ||||||
chr4:145552890
|
A | G | 58 | a0001c0001t0003g0003a0001c0001t0003g0004a0001c0001t0003g0014others(55): Show | 64 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.998-894A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145552890 | ||||||
chr4:145552892
|
ATGT | A | 86 | a0001c0001t0001g0093a0001c0001t0001g0122a0001c0001t0001g0138others(83): Show | 90 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(87): Show |
intron_variant | MODIFIER | c.998-866_998-864del others(3): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr4 | 145552892 | |||||
chr4:145553079
|
A | AT | 147 | a0001c0001t0001g0093a0001c0001t0001g0122a0001c0001t0001g0138others(144): Show | 157 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(154): Show |
intron_variant | MODIFIER | c.998-690dupT | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr4 | 145553079 | |||||
chr4:145553079
|
A | ATT | 19 | a0001c0001t0005g0020a0001c0001t0005g0021a0001c0001t0005g0022others(16): Show | 19 | HG00438.hp1 HG01243.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.998-691_998-690dup others(2): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr4 | 145553079 | |||||
chr4:145553093
|
T | G | 2 | a0001c0001t0009g0286a0001c0001t0018g0281 | 2 | HG01169.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.998-691T>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145553093 | ||||||
chr4:145553093
|
T | TG | 3 | a0001c0001t0010g0132a0001c0001t0010g0251a0001c0001t0015g0147 | 3 | HG01167.hp2 HG01169.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.998-691_998-690ins others(1): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145553093 | ||||||
chr4:145553097
|
G | A | 2 | a0001c0001t0021g0027a0001c0001t0021g0028 | 2 | HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.998-687G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145553097 | ||||||
chr4:145553114
|
G | A | 13 | a0001c0001t0006g0118a0001c0001t0006g0119a0001c0001t0006g0120others(10): Show | 13 | HG00738.hp2 HG01081.hp2 HG03654.hp1 others(10): Show |
intron_variant | MODIFIER | c.998-670G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145553114 | ||||||
chr4:145553150
|
A | G | 5 | a0001c0001t0008g0016a0001c0001t0008g0051a0001c0001t0008g0155others(2): Show | 6 | HG01192.hp2 HG01496.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.998-634A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145553150 | ||||||
chr4:145553281
|
G | A | 1 | a0001c0001t0003g0237 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.998-503G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145553281 | ||||||
chr4:145553292
|
AT | A | 168 | a0001c0001t0001g0093a0001c0001t0001g0122a0001c0001t0001g0138others(165): Show | 178 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(175): Show |
intron_variant | MODIFIER | c.998-487delT | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr4 | 145553292 | |||||
chr4:145553449
|
G | A | 1 | a0001c0001t0021g0027 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.998-335G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145553449 | ||||||
chr4:145553452
|
A | G | 1 | a0001c0001t0001g0018 | 2 | HG01928.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.998-332A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145553452 | ||||||
chr4:145553652
|
C | T | 1 | a0001c0001t0013g0037 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.998-132C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145553652 | ||||||
chr4:145553690
|
C | A | 3 | a0001c0001t0017g0162a0001c0001t0017g0163a0001c0001t0017g0164 | 3 | HG02055.hp2 HG02280.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.998-94C>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145553690 | ||||||
chr4:145553690
|
C | T | 23 | a0001c0001t0005g0020a0001c0001t0005g0021a0001c0001t0005g0022others(20): Show | 24 | HG00438.hp1 HG01243.hp2 HG01261.hp1 others(21): Show |
intron_variant | MODIFIER | c.998-94C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 5/6 | chr4 | 145553690 | ||||||
chr4:145554091
|
C | CT | 7 | a0001c0001t0001g0146a0001c0001t0002g0084a0001c0001t0002g0087others(4): Show | 7 | HG00558.hp1 HG01934.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.1254+68dupT | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr4 | 145554091 | |||||
chr4:145554091
|
CT | C | 89 | a0001c0001t0001g0017a0001c0001t0001g0264a0001c0001t0002g0185others(86): Show | 95 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.1254+68delT | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr4 | 145554091 | |||||
chr4:145554335
|
T | G | 1 | a0001c0001t0002g0182 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1254+295T>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 6/6 | chr4 | 145554335 | ||||||
chr4:145554423
|
A | T | 1 | a0001c0001t0002g0012 | 2 | HG01981.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.1254+383A>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 6/6 | chr4 | 145554423 | ||||||
chr4:145554652
|
A | T | 1 | a0001c0001t0002g0182 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1254+612A>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 6/6 | chr4 | 145554652 | ||||||
chr4:145554825
|
T | C | 93 | a0001c0001t0001g0034a0001c0001t0001g0064a0001c0001t0001g0065others(90): Show | 97 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(94): Show |
intron_variant | MODIFIER | c.1254+785T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 6/6 | chr4 | 145554825 | ||||||
chr4:145555086
|
T | G | 1 | a0001c0001t0002g0182 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1254+1046T>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 6/6 | chr4 | 145555086 | ||||||
chr4:145555089
|
G | T | 1 | a0001c0001t0002g0182 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1254+1049G>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 6/6 | chr4 | 145555089 | ||||||
chr4:145555090
|
T | G | 1 | a0001c0001t0002g0182 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1254+1050T>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 6/6 | chr4 | 145555090 | ||||||
chr4:145555469
|
G | A | 86 | a0001c0001t0001g0093a0001c0001t0001g0122a0001c0001t0001g0138others(83): Show | 90 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(87): Show |
intron_variant | MODIFIER | c.1254+1429G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 6/6 | chr4 | 145555469 | ||||||
chr4:145555494
|
G | T | 1 | a0001c0001t0006g0223 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1254+1454G>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 6/6 | chr4 | 145555494 | ||||||
chr4:145555552
|
T | G | 1 | a0001c0002t0012g0050 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1254+1512T>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 6/6 | chr4 | 145555552 | ||||||
chr4:145555559
|
T | C | 1 | a0001c0001t0002g0173 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1254+1519T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 6/6 | chr4 | 145555559 | ||||||
chr4:145555678
|
TTACACTA others(22): Show |
T | 2 | a0001c0001t0003g0129a0001c0001t0003g0244 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1254+1639_1254+166 others(33): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 6/6 | chr4 | 145555678 | ||||||
chr4:145555760
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A | C | 4 | a0001c0001t0014g0039a0001c0001t0014g0066a0001c0001t0014g0067others(1): Show | 4 | HG02145.hp2 HG02451.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1254+1720A>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 6/6 | chr4 | 145555760 | ||||||
chr4:145555761
|
C | T | 4 | a0001c0001t0014g0039a0001c0001t0014g0066a0001c0001t0014g0067others(1): Show | 4 | HG02145.hp2 HG02451.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1254+1721C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 6/6 | chr4 | 145555761 | ||||||
chr4:145555906
|
T | C | 88 | a0001c0001t0001g0034a0001c0001t0001g0064a0001c0001t0001g0065others(85): Show | 92 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.1254+1866T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 6/6 | chr4 | 145555906 | ||||||
chr4:145556112
|
G | A | 1 | a0001c0001t0002g0088 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1255-1679G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 6/6 | chr4 | 145556112 | ||||||
chr4:145556267
|
A | G | 1 | a0001c0001t0002g0166 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1255-1524A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 6/6 | chr4 | 145556267 | ||||||
chr4:145556278
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T | A | 88 | a0001c0001t0001g0034a0001c0001t0001g0064a0001c0001t0001g0065others(85): Show | 92 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.1255-1513T>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 6/6 | chr4 | 145556278 | ||||||
chr4:145556307
|
G | C | 4 | a0001c0001t0015g0076a0001c0001t0015g0147a0001c0001t0015g0148others(1): Show | 4 | HG03453.hp1 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1255-1484G>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 6/6 | chr4 | 145556307 | ||||||
chr4:145556372
|
G | T | 3 | a0001c0001t0006g0222a0001c0001t0006g0223a0001c0001t0006g0224 | 3 | HG01081.hp2 HG03942.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1255-1419G>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 6/6 | chr4 | 145556372 | ||||||
chr4:145556515
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G | A | 2 | a0001c0001t0001g0266a0001c0001t0002g0184 | 2 | HG01261.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1255-1276G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 6/6 | chr4 | 145556515 | ||||||
chr4:145556582
|
A | G | 169 | a0001c0001t0001g0093a0001c0001t0001g0122a0001c0001t0001g0138others(166): Show | 179 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.1255-1209A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 6/6 | chr4 | 145556582 | ||||||
chr4:145556768
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A | G | 168 | a0001c0001t0001g0093a0001c0001t0001g0122a0001c0001t0001g0138others(165): Show | 178 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(175): Show |
intron_variant | MODIFIER | c.1255-1023A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 6/6 | chr4 | 145556768 | ||||||
chr4:145556878
|
A | G | 4 | a0001c0001t0006g0120a0001c0001t0006g0126a0001c0001t0006g0225others(1): Show | 4 | NA18952.hp1 NA18973.hp1 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.1255-913A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 6/6 | chr4 | 145556878 | ||||||
chr4:145556905
|
C | T | 13 | a0001c0001t0006g0118a0001c0001t0006g0119a0001c0001t0006g0120others(10): Show | 13 | HG00738.hp2 HG01081.hp2 HG03654.hp1 others(10): Show |
intron_variant | MODIFIER | c.1255-886C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 6/6 | chr4 | 145556905 | ||||||
chr4:145557037
|
CCTT | C | 86 | a0001c0001t0001g0093a0001c0001t0001g0122a0001c0001t0001g0138others(83): Show | 90 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(87): Show |
intron_variant | MODIFIER | c.1255-751_1255-749d others(5): Show |
SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr4 | 145557037 | |||||
chr4:145557051
|
C | A | 86 | a0001c0001t0001g0093a0001c0001t0001g0122a0001c0001t0001g0138others(83): Show | 90 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(87): Show |
intron_variant | MODIFIER | c.1255-740C>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 6/6 | chr4 | 145557051 | ||||||
chr4:145557068
|
T | C | 1 | a0001c0001t0014g0067 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1255-723T>C | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 6/6 | chr4 | 145557068 | ||||||
chr4:145557180
|
G | A | 2 | a0001c0001t0020g0077a0001c0001t0020g0153 | 2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1255-611G>A | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 6/6 | chr4 | 145557180 | ||||||
chr4:145557230
|
A | G | 2 | a0001c0003t0012g0072a0001c0003t0012g0144 | 2 | HG01884.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1255-561A>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 6/6 | chr4 | 145557230 | ||||||
chr4:145557315
|
C | T | 89 | a0001c0001t0001g0093a0001c0001t0001g0122a0001c0001t0001g0138others(86): Show | 93 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.1255-476C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 6/6 | chr4 | 145557315 | ||||||
chr4:145557391
|
T | G | 90 | a0001c0001t0001g0093a0001c0001t0001g0122a0001c0001t0001g0138others(87): Show | 94 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(91): Show |
intron_variant | MODIFIER | c.1255-400T>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 6/6 | chr4 | 145557391 | ||||||
chr4:145557513
|
C | G | 13 | a0001c0001t0006g0118a0001c0001t0006g0119a0001c0001t0006g0120others(10): Show | 13 | HG00738.hp2 HG01081.hp2 HG03654.hp1 others(10): Show |
intron_variant | MODIFIER | c.1255-278C>G | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 6/6 | chr4 | 145557513 | ||||||
chr4:145557522
|
G | T | 1 | a0001c0001t0001g0139 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1255-269G>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 6/6 | chr4 | 145557522 | ||||||
chr4:145557627
|
C | T | 229 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0018others(226): Show | 243 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.1255-164C>T | SMAD1 | ENSG00000170365.10 | transcript | ENST00000302085.9 | protein_coding | 6/6 | chr4 | 145557627 |