Variant report
Variant | rs58474078 |
---|---|
Chromosome Location | chr7:84353923-84353924 |
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] |
---|---|
rs10155838 | 0.85[AMR][1000 genomes];0.94[ASN][1000 genomes] |
rs10226259 | 0.85[AMR][1000 genomes];0.94[ASN][1000 genomes] |
rs10226299 | 0.85[AMR][1000 genomes];0.94[ASN][1000 genomes] |
rs10231229 | 0.85[AMR][1000 genomes];0.89[ASN][1000 genomes] |
rs10234675 | 0.85[AMR][1000 genomes];0.91[ASN][1000 genomes] |
rs10235779 | 0.85[AMR][1000 genomes];0.94[ASN][1000 genomes] |
rs10236624 | 0.85[AMR][1000 genomes];0.91[ASN][1000 genomes] |
rs10240135 | 0.85[AMR][1000 genomes];0.94[ASN][1000 genomes] |
rs10244742 | 0.85[AMR][1000 genomes];0.94[ASN][1000 genomes] |
rs10249541 | 0.85[AMR][1000 genomes];0.94[ASN][1000 genomes] |
rs10253824 | 0.85[AFR][1000 genomes];0.84[AMR][1000 genomes];0.90[ASN][1000 genomes] |
rs10253977 | 0.85[AMR][1000 genomes];0.92[ASN][1000 genomes] |
rs10258050 | 0.85[AMR][1000 genomes];0.87[ASN][1000 genomes] |
rs10260013 | 0.85[AMR][1000 genomes];0.89[ASN][1000 genomes] |
rs10263930 | 0.85[AMR][1000 genomes];0.89[ASN][1000 genomes] |
rs10264994 | 0.85[AMR][1000 genomes];0.89[ASN][1000 genomes] |
rs10266193 | 0.85[AMR][1000 genomes];0.93[ASN][1000 genomes] |
rs10268436 | 0.85[AMR][1000 genomes];0.87[ASN][1000 genomes] |
rs10268834 | 0.85[AMR][1000 genomes];0.94[ASN][1000 genomes] |
rs10269265 | 0.85[AMR][1000 genomes];0.94[ASN][1000 genomes] |
rs10270396 | 0.96[AMR][1000 genomes];0.94[ASN][1000 genomes] |
rs10270546 | 0.85[AMR][1000 genomes];0.91[ASN][1000 genomes] |
rs10270873 | 0.82[AMR][1000 genomes];0.94[ASN][1000 genomes] |
rs10271786 | 0.85[AMR][1000 genomes];0.93[ASN][1000 genomes] |
rs10274807 | 0.85[AMR][1000 genomes];0.89[ASN][1000 genomes] |
rs10480534 | 0.84[AMR][1000 genomes];0.95[ASN][1000 genomes] |
rs13438201 | 0.96[AMR][1000 genomes];0.98[ASN][1000 genomes] |
rs13438429 | 0.84[AMR][1000 genomes];0.94[ASN][1000 genomes] |
rs1583140 | 0.85[AMR][1000 genomes];0.93[ASN][1000 genomes] |
rs1583141 | 0.85[AMR][1000 genomes];0.93[ASN][1000 genomes] |
rs1594376 | 0.85[AMR][1000 genomes];0.89[ASN][1000 genomes] |
rs1594377 | 0.85[AMR][1000 genomes];0.89[ASN][1000 genomes] |
rs28408003 | 0.85[AMR][1000 genomes];0.94[ASN][1000 genomes] |
rs28439673 | 0.85[AMR][1000 genomes];0.91[ASN][1000 genomes] |
rs28448564 | 0.85[AMR][1000 genomes];0.94[ASN][1000 genomes] |
rs28674967 | 0.82[AMR][1000 genomes];0.89[ASN][1000 genomes] |
rs28735889 | 0.85[AMR][1000 genomes];0.94[ASN][1000 genomes] |
rs28804974 | 0.85[AMR][1000 genomes];0.93[ASN][1000 genomes] |
rs28852818 | 0.85[AMR][1000 genomes];0.93[ASN][1000 genomes] |
rs4128624 | 0.90[AFR][1000 genomes];0.89[AMR][1000 genomes];0.95[ASN][1000 genomes] |
rs4283992 | 0.80[AMR][1000 genomes] |
rs4358754 | 0.85[AMR][1000 genomes];0.93[ASN][1000 genomes] |
rs4439049 | 0.80[AMR][1000 genomes];0.86[ASN][1000 genomes] |
rs4443588 | 0.85[AMR][1000 genomes];0.94[ASN][1000 genomes] |
rs4604378 | 0.83[ASN][1000 genomes] |
rs4620233 | 0.85[AMR][1000 genomes];0.94[ASN][1000 genomes] |
rs4728561 | 0.85[AMR][1000 genomes];0.94[ASN][1000 genomes] |
rs4728562 | 0.85[AMR][1000 genomes];0.94[ASN][1000 genomes] |
rs4732584 | 0.80[AMR][1000 genomes] |
rs4732586 | 0.85[AMR][1000 genomes];0.94[ASN][1000 genomes] |
rs57219677 | 0.85[ASN][1000 genomes] |
rs57297444 | 0.91[AMR][1000 genomes];0.90[ASN][1000 genomes] |
rs57745821 | 0.85[AMR][1000 genomes];0.92[ASN][1000 genomes] |
rs58175686 | 0.89[ASN][1000 genomes] |
rs58333240 | 0.93[ASN][1000 genomes] |
rs6943231 | 0.84[AMR][1000 genomes];0.93[ASN][1000 genomes] |
rs6947577 | 0.82[AMR][1000 genomes];0.93[ASN][1000 genomes] |
rs6947596 | 0.85[AMR][1000 genomes];0.93[ASN][1000 genomes] |
rs6957762 | 0.85[AMR][1000 genomes];0.93[ASN][1000 genomes] |
rs6975316 | 0.85[AMR][1000 genomes];0.94[ASN][1000 genomes] |
rs73712817 | 0.95[AMR][1000 genomes] |
rs7781015 | 0.85[AMR][1000 genomes];0.89[ASN][1000 genomes] |
rs7788552 | 0.84[AMR][1000 genomes];0.85[ASN][1000 genomes] |
rs7793020 | 0.85[AMR][1000 genomes];0.91[ASN][1000 genomes] |
rs7796908 | 0.85[AMR][1000 genomes];0.91[ASN][1000 genomes] |
rs7797337 | 0.85[AMR][1000 genomes];0.93[ASN][1000 genomes] |
rs7797505 | 0.85[AMR][1000 genomes];0.93[ASN][1000 genomes] |
rs7801427 | 0.89[ASN][1000 genomes] |
rs7809245 | 0.85[AMR][1000 genomes];0.91[ASN][1000 genomes] |
rs7810914 | 0.85[AMR][1000 genomes];0.93[ASN][1000 genomes] |
rs891484 | 0.85[AMR][1000 genomes];0.91[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv529344 | chr7:83714286-84592857 | Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 15 gene(s) | inside rSNPs | diseases |
2 | nsv949446 | chr7:84003501-84763823 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 20 gene(s) | inside rSNPs | diseases |
3 | nsv1031149 | chr7:84144990-84404356 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 10 gene(s) | inside rSNPs | diseases |
4 | nsv888641 | chr7:84168615-84453100 | Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
5 | nsv1031328 | chr7:84182356-84377593 | Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
6 | nsv1016221 | chr7:84183142-84377593 | Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
7 | nsv888643 | chr7:84196258-84453100 | Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
8 | nsv1019814 | chr7:84208284-84369045 | Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
9 | esv2762684 | chr7:84218035-84444871 | Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers | TF binding regionCpG islandChromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
10 | nsv831047 | chr7:84231938-84408081 | Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers Strong transcription | TF binding regionCpG islandChromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
11 | nsv888644 | chr7:84253690-84386060 | Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer | TF binding regionCpG islandChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
12 | nsv831049 | chr7:84277599-84475710 | Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
13 | esv34238 | chr7:84279023-84591966 | Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Strong transcription Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr7:84351400-84358400 | Weak transcription | Muscle Satellite Cultured Cells | -- |
2 | chr7:84352200-84355000 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |