Variant report
Variant | rs7549175 |
---|---|
Chromosome Location | chr1:152372355-152372356 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:2)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:2 , 50 per page) page:
1
No data |
No data |
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Variant related genes | Relation type |
---|---|
ENSG00000118418 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs10157860 | 1.00[EUR][1000 genomes] |
rs11805976 | 1.00[EUR][1000 genomes] |
rs11807452 | 1.00[EUR][1000 genomes] |
rs11807465 | 1.00[EUR][1000 genomes] |
rs11810565 | 1.00[EUR][1000 genomes] |
rs12062763 | 1.00[EUR][1000 genomes] |
rs12068970 | 1.00[EUR][1000 genomes] |
rs12071768 | 1.00[EUR][1000 genomes] |
rs12076464 | 1.00[EUR][1000 genomes] |
rs16833974 | 1.00[EUR][1000 genomes] |
rs3120668 | 1.00[EUR][1000 genomes] |
rs3120669 | 1.00[EUR][1000 genomes] |
rs477291 | 1.00[EUR][1000 genomes] |
rs506407 | 1.00[EUR][1000 genomes] |
rs58782040 | 1.00[EUR][1000 genomes] |
rs60958057 | 1.00[EUR][1000 genomes] |
rs61250742 | 1.00[EUR][1000 genomes] |
rs61676926 | 1.00[EUR][1000 genomes] |
rs61749580 | 1.00[EUR][1000 genomes] |
rs6587670 | 1.00[EUR][1000 genomes] |
rs6667236 | 1.00[EUR][1000 genomes] |
rs6669029 | 1.00[EUR][1000 genomes] |
rs6673073 | 1.00[EUR][1000 genomes] |
rs6681629 | 1.00[EUR][1000 genomes] |
rs6695830 | 1.00[EUR][1000 genomes] |
rs72997398 | 1.00[EUR][1000 genomes] |
rs72999303 | 1.00[EUR][1000 genomes] |
rs73001316 | 1.00[EUR][1000 genomes] |
rs73001318 | 1.00[EUR][1000 genomes] |
rs73001319 | 1.00[EUR][1000 genomes] |
rs73001326 | 1.00[EUR][1000 genomes] |
rs73001329 | 1.00[EUR][1000 genomes] |
rs73001338 | 1.00[EUR][1000 genomes] |
rs73007787 | 1.00[EUR][1000 genomes] |
rs73007794 | 1.00[EUR][1000 genomes] |
rs73007801 | 1.00[EUR][1000 genomes] |
rs7514641 | 1.00[EUR][1000 genomes] |
rs7515573 | 1.00[YRI][hapmap];0.87[AFR][1000 genomes] |
rs7554863 | 1.00[EUR][1000 genomes] |
rs9725444 | 1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1014095 | chr1:152104486-152454591 | Active TSS Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 28 gene(s) | inside rSNPs | diseases |
2 | nsv1005472 | chr1:152247763-152443448 | Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 23 gene(s) | inside rSNPs | diseases |
3 | nsv535161 | chr1:152247763-152443448 | Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 23 gene(s) | inside rSNPs | diseases |
4 | nsv916016 | chr1:152337775-152590520 | Weak transcription Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 16 gene(s) | inside rSNPs | diseases |
No data |