Variant report
Variant | rs6854158 |
---|---|
Chromosome Location | chr4:148618467-148618468 |
allele | A/G |
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 |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10003944 | 1.00[EUR][1000 genomes] |
rs10012917 | 1.00[EUR][1000 genomes] |
rs10017079 | 1.00[EUR][1000 genomes] |
rs10020557 | 1.00[EUR][1000 genomes] |
rs10024734 | 1.00[EUR][1000 genomes] |
rs10031628 | 1.00[EUR][1000 genomes] |
rs10305926 | 1.00[EUR][1000 genomes] |
rs1105266 | 1.00[EUR][1000 genomes] |
rs11933787 | 1.00[EUR][1000 genomes] |
rs11934646 | 1.00[AMR][1000 genomes] |
rs11935436 | 1.00[EUR][1000 genomes] |
rs11939191 | 1.00[EUR][1000 genomes] |
rs11940536 | 1.00[EUR][1000 genomes] |
rs1503863 | 1.00[EUR][1000 genomes] |
rs1517135 | 1.00[EUR][1000 genomes] |
rs17023736 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs17023827 | 1.00[AMR][1000 genomes] |
rs2036499 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs2036502 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs2358096 | 1.00[EUR][1000 genomes] |
rs2654947 | 0.91[YRI][hapmap] |
rs2718451 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs28551143 | 1.00[EUR][1000 genomes] |
rs6535547 | 1.00[YRI][hapmap] |
rs6535551 | 1.00[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs6824884 | 1.00[EUR][1000 genomes] |
rs6848211 | 1.00[AMR][1000 genomes] |
rs7663257 | 1.00[AMR][1000 genomes] |
rs7673515 | 1.00[EUR][1000 genomes] |
rs7681275 | 1.00[EUR][1000 genomes] |
rs7699281 | 1.00[AMR][1000 genomes] |
rs9308219 | 1.00[EUR][1000 genomes] |
rs9308220 | 1.00[EUR][1000 genomes] |
rs9308221 | 1.00[EUR][1000 genomes] |
rs931779 | 1.00[EUR][1000 genomes] |
rs9884319 | 1.00[EUR][1000 genomes] |
rs9884495 | 1.00[EUR][1000 genomes] |
rs9997823 | 1.00[EUR][1000 genomes] |
rs9999853 | 1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1028958 | chr4:148377752-148793485 | Weak transcription Strong transcription Enhancers Active TSS Genic enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 21 gene(s) | inside rSNPs | diseases |
2 | nsv498083 | chr4:148519825-148917583 | Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 20 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr4:148617600-148618600 | Enhancers | Placenta | Placenta |
2 | chr4:148618000-148618600 | Enhancers | NHEK | skin |