Variant report
Variant | rs6948174 |
---|---|
Chromosome Location | chr7:69511919-69511920 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
No data |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs1000874 | 0.81[EUR][1000 genomes] |
rs10081305 | 0.91[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs10085908 | 0.91[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs10156142 | 0.97[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs1017113 | 1.00[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs10215914 | 0.92[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs10216097 | 0.84[EUR][1000 genomes] |
rs10216186 | 0.94[EUR][1000 genomes] |
rs10227424 | 0.91[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs10228786 | 0.97[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs10229336 | 0.94[EUR][1000 genomes] |
rs10234106 | 0.91[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs10234121 | 1.00[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs10235098 | 0.94[EUR][1000 genomes] |
rs10238049 | 1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs10239569 | 0.84[EUR][1000 genomes] |
rs10243408 | 0.81[EUR][1000 genomes] |
rs10245690 | 0.84[EUR][1000 genomes] |
rs10245749 | 0.94[EUR][1000 genomes] |
rs10248401 | 0.97[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs10248606 | 0.91[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs10251433 | 0.87[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs10254871 | 0.97[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs10256093 | 0.91[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs10258846 | 0.94[EUR][1000 genomes] |
rs10259028 | 0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs10262102 | 0.97[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs10266802 | 1.00[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs10272781 | 0.84[EUR][1000 genomes] |
rs10274419 | 0.84[EUR][1000 genomes] |
rs10275721 | 0.84[EUR][1000 genomes] |
rs10276322 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs10276912 | 0.91[EUR][1000 genomes] |
rs10278001 | 0.94[EUR][1000 genomes] |
rs10278978 | 0.84[EUR][1000 genomes] |
rs10279669 | 0.84[EUR][1000 genomes] |
rs10281537 | 0.97[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs10452739 | 0.94[EUR][1000 genomes] |
rs10487943 | 0.84[EUR][1000 genomes] |
rs10950193 | 0.91[EUR][1000 genomes] |
rs11762487 | 0.94[EUR][1000 genomes] |
rs11763426 | 0.85[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs11764141 | 0.91[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs11764397 | 0.97[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs11764911 | 1.00[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs11766424 | 0.91[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs11766980 | 1.00[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs11768151 | 1.00[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs11769033 | 0.81[EUR][1000 genomes] |
rs11769390 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs11770241 | 0.91[EUR][1000 genomes] |
rs11770380 | 0.91[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs11770466 | 0.85[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs11770695 | 1.00[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs11771751 | 0.81[EUR][1000 genomes] |
rs11771768 | 1.00[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs11771899 | 0.84[EUR][1000 genomes] |
rs12113743 | 0.82[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs12333653 | 0.94[EUR][1000 genomes] |
rs13437638 | 0.97[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs17140938 | 0.84[EUR][1000 genomes] |
rs17141032 | 0.94[EUR][1000 genomes] |
rs17141168 | 1.00[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs17141181 | 0.97[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs17141191 | 0.97[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs17141193 | 0.97[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs17361825 | 0.81[EUR][1000 genomes] |
rs28393394 | 0.94[EUR][1000 genomes] |
rs28433534 | 0.97[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs28464032 | 0.91[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs28489338 | 0.97[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs28496072 | 0.94[EUR][1000 genomes] |
rs28502437 | 0.94[EUR][1000 genomes] |
rs28582872 | 0.91[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs28617759 | 0.82[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs28630917 | 1.00[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs28657792 | 0.97[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs2865804 | 0.81[EUR][1000 genomes] |
rs2866276 | 0.82[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs28812289 | 0.84[EUR][1000 genomes] |
rs28864527 | 0.94[EUR][1000 genomes] |
rs34080361 | 0.81[EUR][1000 genomes] |
rs35862187 | 0.84[EUR][1000 genomes] |
rs3800979 | 0.81[EUR][1000 genomes] |
rs4364526 | 0.91[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs4557583 | 0.97[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs56063609 | 0.82[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs56272534 | 0.92[ASN][1000 genomes] |
rs56376205 | 0.91[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs56388246 | 0.82[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs56405888 | 0.85[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs56999082 | 0.97[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs57370717 | 0.82[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs58666988 | 0.81[EUR][1000 genomes] |
rs60847182 | 0.82[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs6944701 | 0.91[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs6950849 | 0.85[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs6958450 | 0.81[EUR][1000 genomes] |
rs6958714 | 0.94[EUR][1000 genomes] |
rs6961682 | 0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs6967512 | 0.91[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs6968426 | 0.94[EUR][1000 genomes] |
rs6976263 | 0.91[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs6978818 | 0.94[EUR][1000 genomes] |
rs719294 | 0.81[EUR][1000 genomes] |
rs73154605 | 0.84[EUR][1000 genomes] |
rs73160193 | 0.97[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs73168739 | 0.81[EUR][1000 genomes] |
rs73168740 | 0.84[EUR][1000 genomes] |
rs73168747 | 0.94[EUR][1000 genomes] |
rs73168758 | 0.94[EUR][1000 genomes] |
rs73171731 | 0.91[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs740946 | 0.81[EUR][1000 genomes] |
rs7777243 | 0.91[EUR][1000 genomes] |
rs7777621 | 0.81[EUR][1000 genomes] |
rs7780665 | 0.85[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs7780835 | 0.84[EUR][1000 genomes] |
rs7781664 | 0.94[EUR][1000 genomes] |
rs7784950 | 0.84[EUR][1000 genomes] |
rs7796273 | 0.85[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs7797662 | 0.91[EUR][1000 genomes] |
rs7798890 | 1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs7805165 | 0.97[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs7806413 | 0.91[EUR][1000 genomes] |
rs9690738 | 0.94[EUR][1000 genomes] |
rs9690769 | 0.94[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1021538 | chr7:69130236-69575753 | Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
2 | nsv538917 | chr7:69130236-69575753 | Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
3 | nsv817276 | chr7:69130237-69736834 | Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
4 | nsv1018749 | chr7:69149029-69995112 | Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
5 | nsv492242 | chr7:69330737-69520566 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Strong transcription Genic enhancers | Chromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
6 | nsv1018289 | chr7:69383450-69650885 | Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats Active TSS Strong transcription Genic enhancers | Chromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
7 | nsv538922 | chr7:69383450-69650885 | Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers | Chromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
8 | nsv532782 | chr7:69383651-70189959 | Weak transcription Genic enhancers Enhancers Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
9 | nsv1034281 | chr7:69403828-69548378 | Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers | Chromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
10 | nsv538923 | chr7:69403828-69548378 | Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers | Chromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
11 | nsv1034182 | chr7:69406172-69529294 | Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers | Chromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
12 | nsv538924 | chr7:69406172-69529294 | Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers | Chromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
13 | esv2758119 | chr7:69412504-69594161 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers | Chromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
14 | esv2759536 | chr7:69412504-69594161 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers | Chromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
15 | nsv607429 | chr7:69430748-69553093 | Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer | Chromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
16 | nsv1028705 | chr7:69453983-69524628 | Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
17 | nsv1020488 | chr7:69465268-69671126 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer Strong transcription | Chromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
18 | nsv1022932 | chr7:69496659-69564369 | ZNF genes & repeats Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
19 | nsv538925 | chr7:69496659-69564369 | Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
20 | nsv1034817 | chr7:69507871-69578892 | Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
21 | nsv538926 | chr7:69507871-69578892 | Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr7:69505800-69513200 | Weak transcription | hESC Derived CD56+ Mesoderm Cultured Cells | ES cell derived |
2 | chr7:69506200-69512400 | Weak transcription | iPS-15b Cell Line | embryonic stem cell |
3 | chr7:69507200-69512800 | Weak transcription | HUES64 Cell Line | embryonic stem cell |
4 | chr7:69508000-69513000 | Weak transcription | H9 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
5 | chr7:69508400-69512400 | Weak transcription | Fetal Lung | lung |
6 | chr7:69508400-69513000 | Weak transcription | Ganglion Eminence derived primary cultured neurospheres | brain |
7 | chr7:69509400-69512400 | Weak transcription | H1 Cell Line | embryonic stem cell |
8 | chr7:69509400-69512400 | Weak transcription | iPS-18 Cell Line | embryonic stem cell |
9 | chr7:69509400-69512600 | Weak transcription | HUES6 Cell Line | embryonic stem cell |
10 | chr7:69509400-69513000 | Weak transcription | Fetal Adrenal Gland | Adrenal Gland |
11 | chr7:69509400-69513000 | Weak transcription | Fetal Stomach | stomach |
12 | chr7:69509600-69512200 | Weak transcription | iPS-20b Cell Line | embryonic stem cell |
13 | chr7:69509600-69512600 | Weak transcription | ES-I3 Cell Line | embryonic stem cell |
14 | chr7:69509600-69512800 | Weak transcription | HUES48 Cell Line | embryonic stem cell |
15 | chr7:69510400-69517400 | Weak transcription | Pancreatic Islets | Pancreatic Islet |
16 | chr7:69511400-69512600 | Weak transcription | Fetal Intestine Large | intestine |
17 | chr7:69511600-69512000 | Weak transcription | Fetal Intestine Small | intestine |