Variant report
Variant | rs62373462 |
---|---|
Chromosome Location | chr5:98449216-98449217 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:1)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:1 , 50 per page) page:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr16:12069041..12070712-chr5:98447812..98450049,2 | MCF-7 | breast: |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000234719 | Chromatin interaction |
ENSG00000048471 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs10057971 | 0.86[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs10059861 | 0.88[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs10067087 | 0.86[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10477871 | 0.85[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs10515286 | 0.82[AFR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11738104 | 0.88[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11738286 | 0.82[ASN][1000 genomes] |
rs11743338 | 0.82[ASN][1000 genomes] |
rs1348926 | 0.89[ASN][1000 genomes] |
rs1447378 | 0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1447383 | 0.81[AMR][1000 genomes];0.89[ASN][1000 genomes] |
rs17166635 | 0.89[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs2369575 | 0.82[ASN][1000 genomes] |
rs34218854 | 0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs3866454 | 0.84[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs4035624 | 0.85[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs61344339 | 0.82[ASN][1000 genomes] |
rs62376621 | 0.81[AFR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs6884259 | 0.82[ASN][1000 genomes] |
rs6896400 | 0.82[ASN][1000 genomes] |
rs7724878 | 0.83[EUR][1000 genomes];0.86[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1024391 | chr5:98355665-98653657 | Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh | Chromatin interactive region | 5 gene(s) | inside rSNPs | diseases |
2 | nsv599118 | chr5:98358191-99029453 | Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
3 | nsv599119 | chr5:98358191-99315677 | Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 13 gene(s) | inside rSNPs | diseases |
4 | nsv882417 | chr5:98428184-98548315 | Weak transcription Enhancers Flanking Active TSS | Chromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
5 | nsv482367 | chr5:98440337-98606909 | Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats | Chromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
6 | nsv882418 | chr5:98447682-98694849 | Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS | Chromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
No data |