Variant report

Variant	rs11780484
Chromosome Location	chr8:39684680-39684681
allele	A/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:16)

rs_ID	r²[population]
rs10090488	0.82[ASN][1000 genomes]
rs10099876	1.00[CHB][hapmap]
rs10104554	1.00[CHB][hapmap]
rs11775094	0.92[EUR][1000 genomes]
rs11779433	0.86[EUR][1000 genomes]
rs62511208	0.90[EUR][1000 genomes]
rs62511246	0.92[EUR][1000 genomes]
rs6988758	0.81[CEU][hapmap]
rs73615878	1.00[ASN][1000 genomes]
rs73673810	0.91[ASN][1000 genomes]
rs73673831	1.00[ASN][1000 genomes]
rs73673836	1.00[ASN][1000 genomes]
rs73674773	0.91[ASN][1000 genomes]
rs7816926	1.00[ASN][1000 genomes]
rs7823566	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs7833334	0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1015907	chr8:38967169-39718559	Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv539550	chr8:38967169-39718559	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
3	nsv539555	chr8:39683857-40673606	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:39684600-39685000	Enhancers	Colon Smooth Muscle	Colon

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

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