Variant report
Variant | rs2023548 |
---|---|
Chromosome Location | chr7:99417324-99417325 |
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 | chr7:99415648..99420194-chr7:99515880..99518686,4 | MCF-7 | breast: |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000146833 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs1036374 | 0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs11734 | 1.00[TSI][hapmap] |
rs12535293 | 1.00[GIH][hapmap] |
rs12535919 | 1.00[GIH][hapmap] |
rs17161937 | 1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];0.91[LWK][hapmap];1.00[MEX][hapmap];0.95[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs17161971 | 1.00[GIH][hapmap] |
rs17161974 | 1.00[GIH][hapmap] |
rs17161981 | 1.00[GIH][hapmap] |
rs17161983 | 1.00[GIH][hapmap] |
rs1851426 | 1.00[CEU][hapmap];0.91[EUR][1000 genomes] |
rs2103030 | 0.91[EUR][1000 genomes] |
rs2461610 | 0.91[EUR][1000 genomes] |
rs2687105 | 1.00[CEU][hapmap];0.81[EUR][1000 genomes] |
rs2687116 | 0.87[EUR][1000 genomes] |
rs2738262 | 0.91[EUR][1000 genomes] |
rs2740566 | 1.00[CEU][hapmap];1.00[GIH][hapmap];0.91[EUR][1000 genomes] |
rs2740574 | 0.91[EUR][1000 genomes] |
rs28988583 | 0.95[EUR][1000 genomes] |
rs4281055 | 0.87[EUR][1000 genomes] |
rs6956305 | 1.00[TSI][hapmap] |
rs6976017 | 1.00[TSI][hapmap] |
rs73393660 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs892753 | 0.90[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv1827709 | chr7:99353500-99440051 | Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 10 gene(s) | inside rSNPs | diseases |
2 | nsv970418 | chr7:99413271-99420442 | Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer | TF binding regionChromatin interactive region | 4 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr7:99415600-99417400 | Weak transcription | HepG2 | liver |
2 | chr7:99416600-99420000 | Weak transcription | Adipose Nuclei | Adipose |