Variant report
Variant | rs1827655 |
---|---|
Chromosome Location | chr8:122187435-122187436 |
allele | G/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:4)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:4 , 50 per page) page:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr8:122185637..122188529-chr8:122188929..122190914,2 | K562 | blood: | |
2 | chr8:122001411..122003194-chr8:122185252..122188159,2 | MCF-7 | breast: | |
3 | chr8:121997176..121997957-chr8:122187230..122188110,2 | MCF-7 | breast: | |
4 | chr8:122176632..122180030-chr8:122186675..122188884,3 | MCF-7 | breast: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10102893 | 1.00[ASN][1000 genomes] |
rs10104487 | 1.00[ASN][1000 genomes] |
rs10108717 | 0.88[EUR][1000 genomes] |
rs10111630 | 0.89[EUR][1000 genomes] |
rs10505396 | 1.00[ASN][1000 genomes] |
rs10956006 | 0.90[EUR][1000 genomes] |
rs1124090 | 1.00[ASN][1000 genomes] |
rs13258658 | 1.00[ASN][1000 genomes] |
rs1433393 | 0.82[EUR][1000 genomes] |
rs1504658 | 0.96[CEU][hapmap];0.95[EUR][1000 genomes] |
rs1553507 | 1.00[ASN][1000 genomes] |
rs1553508 | 1.00[ASN][1000 genomes] |
rs1560771 | 0.88[EUR][1000 genomes] |
rs1604898 | 0.87[EUR][1000 genomes] |
rs17206976 | 1.00[ASN][1000 genomes] |
rs17262197 | 0.87[EUR][1000 genomes] |
rs2202381 | 1.00[ASN][1000 genomes] |
rs2386267 | 0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2581548 | 1.00[ASN][1000 genomes] |
rs2581549 | 1.00[ASN][1000 genomes] |
rs2581550 | 1.00[ASN][1000 genomes] |
rs2581552 | 1.00[ASN][1000 genomes] |
rs2656110 | 1.00[ASN][1000 genomes] |
rs2656111 | 1.00[ASN][1000 genomes] |
rs2656113 | 1.00[ASN][1000 genomes] |
rs2656114 | 1.00[ASN][1000 genomes] |
rs2656115 | 1.00[ASN][1000 genomes] |
rs2656116 | 1.00[ASN][1000 genomes] |
rs4242325 | 0.86[CEU][hapmap];1.00[CHB][hapmap];0.94[AFR][1000 genomes];0.86[EUR][1000 genomes] |
rs4304334 | 0.87[EUR][1000 genomes] |
rs4871168 | 0.90[EUR][1000 genomes] |
rs4871170 | 0.83[EUR][1000 genomes] |
rs4871171 | 0.83[EUR][1000 genomes] |
rs6469992 | 0.89[EUR][1000 genomes] |
rs6982766 | 1.00[ASN][1000 genomes] |
rs6983966 | 0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6988416 | 1.00[ASN][1000 genomes] |
rs6988639 | 1.00[ASN][1000 genomes] |
rs6989776 | 1.00[ASN][1000 genomes] |
rs7844326 | 0.82[EUR][1000 genomes] |
rs905759 | 1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv891424 | chr8:121873345-122393258 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
2 | esv1844734 | chr8:121928250-122283585 | Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Strong transcription Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
3 | esv3330574 | chr8:122039099-122386130 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
4 | nsv891426 | chr8:122078334-122393258 | Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Genic enhancers Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
5 | nsv1021839 | chr8:122173682-122240824 | Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr8:122185600-122188400 | Weak transcription | Fetal Muscle Leg | muscle |
2 | chr8:122185600-122190400 | Weak transcription | Mesenchymal Stem Cell Derived Adipocyte Cultured Cells | ES cell derived |
3 | chr8:122185800-122190400 | Weak transcription | Muscle Satellite Cultured Cells | -- |
4 | chr8:122186800-122187600 | Weak transcription | HSMM | muscle |