Variant report

Variant	rs73238314
Chromosome Location	chr4:56609315-56609316
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs11726168	0.99[EUR][1000 genomes]
rs11726921	0.91[EUR][1000 genomes]
rs11737856	0.95[EUR][1000 genomes]
rs55767063	0.86[EUR][1000 genomes]
rs66825111	0.82[EUR][1000 genomes]
rs73236191	0.87[EUR][1000 genomes]
rs73236192	0.89[EUR][1000 genomes]
rs73236193	0.91[EUR][1000 genomes]
rs73236200	0.94[EUR][1000 genomes]
rs73236201	0.94[EUR][1000 genomes]
rs73238305	0.95[EUR][1000 genomes]
rs73238306	0.93[EUR][1000 genomes]
rs73238309	0.99[EUR][1000 genomes]
rs73238311	0.99[EUR][1000 genomes]
rs73238312	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73238320	0.98[EUR][1000 genomes]
rs73238321	0.87[EUR][1000 genomes]
rs73238323	0.82[EUR][1000 genomes]
rs9684463	0.92[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2755990	chr4:56317136-57143037	Strong transcription Weak transcription Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
2	nsv10496	chr4:56336946-56841137	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
3	nsv998179	chr4:56425126-56694339	Flanking Active TSS Bivalent/Poised TSS Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	nsv932636	chr4:56438618-56667329	Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	nsv879021	chr4:56482750-56648713	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	nsv1005845	chr4:56522075-56980357	Active TSS Bivalent Enhancer Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
7	esv3406311	chr4:56580578-56840877	ZNF genes & repeats Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:56608800-56609400	Enhancers	Muscle Satellite Cultured Cells	--
2	chr4:56608800-56609400	Enhancers	Ovary	ovary
3	chr4:56608800-56609400	Enhancers	HMEC	breast
4	chr4:56608800-56609400	Enhancers	K562	blood
5	chr4:56608800-56609600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr4:56609000-56609400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr4:56609000-56609600	Enhancers	Fetal Stomach	stomach
8	chr4:56609200-56609400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr4:56609200-56609600	Enhancers	Fetal Muscle Trunk	muscle
10	chr4:56609200-56609600	Enhancers	Fetal Muscle Leg	muscle

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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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