Variant report

Variant	rs11716284
Chromosome Location	chr3:54229165-54229166
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs11707387	0.87[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs11716674	1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs12493260	1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs12630117	1.00[JPT][hapmap]
rs1449336	1.00[JPT][hapmap]
rs4076707	1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs4076709	1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs4373100	1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs4927998	1.00[JPT][hapmap]
rs4928001	1.00[JPT][hapmap]
rs6809942	1.00[JPT][hapmap]
rs73085988	0.87[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs9880023	1.00[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1003621	chr3:53448934-54425322	Active TSS Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
2	nsv1006990	chr3:53849510-54285212	Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
3	nsv1014595	chr3:53944473-54846754	Enhancers Bivalent Enhancer Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv1014157	chr3:54168755-54332321	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv518483	chr3:54212182-54259801	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:54227200-54232200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr3:54227600-54232600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr3:54227800-54232600	Weak transcription	HUES6 Cell Line	embryonic stem cell
4	chr3:54228000-54232200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr3:54229000-54229400	Weak transcription	Brain Germinal Matrix	brain

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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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