Variant report

Variant	rs7863698
Chromosome Location	chr9:105162733-105162734
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs61519830	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73506621	1.00[EUR][1000 genomes]
rs73506631	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1048227	chr9:104546761-105162810	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv831675	chr9:105013834-105184661	Weak transcription Enhancers Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv428541	chr9:105044345-105201140	Weak transcription Enhancers Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	esv2263190	chr9:105162303-105162862	Enhancers	n/a	n/a	inside rSNPs	diseases
5	esv5305	chr9:105162380-105162783	Enhancers	n/a	n/a	inside rSNPs	diseases
6	esv3523369	chr9:105162382-105162774	Enhancers	n/a	n/a	inside rSNPs	diseases
7	esv3523370	chr9:105162412-105162750	Enhancers	n/a	n/a	inside rSNPs	diseases
8	esv3482611	chr9:105162413-105162740	Enhancers	n/a	n/a	inside rSNPs	diseases
9	esv3482610	chr9:105162452-105162737	Enhancers	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:105161800-105163000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr9:105162200-105163000	Enhancers	Breast Myoepithelial Primary Cells	Breast

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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