Variant report
Variant | rs305985 |
---|---|
Chromosome Location | chr19:41613185-41613186 |
allele | G/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 | chr19:41223179..41225407-chr19:41612527..41615194,2 | MCF-7 | breast: |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000123815 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs1173262 | 1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs1645696 | 0.85[AFR][1000 genomes] |
rs1645709 | 0.95[YRI][hapmap];0.91[AFR][1000 genomes] |
rs1645710 | 0.85[YRI][hapmap] |
rs1645712 | 1.00[YRI][hapmap];0.90[AFR][1000 genomes] |
rs1709084 | 0.85[AFR][1000 genomes] |
rs1709085 | 0.85[AFR][1000 genomes] |
rs1709092 | 0.88[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1709093 | 0.86[AFR][1000 genomes] |
rs1709112 | 1.00[YRI][hapmap] |
rs1709113 | 0.85[AFR][1000 genomes] |
rs1709114 | 1.00[YRI][hapmap];0.90[AFR][1000 genomes] |
rs1709115 | 1.00[YRI][hapmap];0.90[AFR][1000 genomes] |
rs184247 | 0.89[AFR][1000 genomes] |
rs2458636 | 0.94[AFR][1000 genomes] |
rs2458638 | 1.00[YRI][hapmap];0.94[AFR][1000 genomes] |
rs2548792 | 1.00[YRI][hapmap];0.94[AFR][1000 genomes] |
rs28447222 | 0.90[AFR][1000 genomes] |
rs305984 | 0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs58285195 | 0.90[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1065684 | chr19:41516389-41644542 | Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 11 gene(s) | inside rSNPs | diseases |
No data |