Variant report

Variant	rs4567609
Chromosome Location	chr13:47853307-47853308
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs11841943	0.83[ASN][1000 genomes]
rs2406324	0.87[ASN][1000 genomes]
rs2406325	0.87[ASN][1000 genomes]
rs2406326	0.88[ASN][1000 genomes]
rs2406327	0.88[ASN][1000 genomes]
rs4531630	0.90[ASN][1000 genomes]
rs7320852	0.88[ASN][1000 genomes]
rs8001945	0.83[ASN][1000 genomes]
rs9526300	0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9526301	0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9526304	0.89[ASN][1000 genomes]
rs9526306	0.88[ASN][1000 genomes]
rs9526307	0.88[ASN][1000 genomes]
rs9534581	0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9567825	0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2763019	chr13:47348229-48123447	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
2	esv3394678	chr13:47678184-48039379	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv832599	chr13:47703075-47873855	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
4	nsv1046560	chr13:47826023-47854425	Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:47852000-47853400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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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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