Variant report

Variant	rs41367045
Chromosome Location	chr4:95858010-95858011
allele	A/C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs11932090	1.00[ASN][1000 genomes]
rs11940026	1.00[ASN][1000 genomes]
rs12512681	1.00[ASN][1000 genomes]
rs13105913	1.00[ASW][hapmap];1.00[CHD][hapmap];0.90[LWK][hapmap];0.87[YRI][hapmap]
rs13119758	0.90[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs13120868	1.00[ASN][1000 genomes]
rs13120952	0.90[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs13122133	0.85[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs13133713	1.00[YRI][hapmap]
rs13138219	1.00[ASN][1000 genomes]
rs13138431	1.00[ASN][1000 genomes]
rs17022671	1.00[CHD][hapmap];1.00[ASN][1000 genomes]
rs17429196	1.00[ASW][hapmap];1.00[CHD][hapmap]
rs17429252	0.87[YRI][hapmap];0.85[AFR][1000 genomes]
rs17501058	1.00[CHD][hapmap]
rs35247579	1.00[ASN][1000 genomes]
rs35716337	1.00[ASN][1000 genomes]
rs35858185	1.00[ASN][1000 genomes]
rs3775009	0.87[ASW][hapmap]
rs67037000	0.85[AFR][1000 genomes]
rs6820744	0.87[ASW][hapmap]
rs6855185	1.00[ASN][1000 genomes]
rs7676775	1.00[ASN][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	nsv932216	chr4:95501261-96109807	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Genic enhancers Strong transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv1003860	chr4:95507683-96120619	Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
3	nsv869528	chr4:95537649-96368018	Weak transcription Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
4	nsv1005816	chr4:95573444-95902704	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
5	nsv492312	chr4:95823124-96128327	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
6	nsv1014420	chr4:95853357-95886153	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
7	nsv537189	chr4:95853357-95886153	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:95849200-95861600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr4:95850800-95861000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr4:95853200-95860800	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr4:95853400-95858200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr4:95856000-95860800	Weak transcription	HUVEC	blood vessel
6	chr4:95856400-95858200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr4:95856400-95858600	Flanking Active TSS	A549	lung
8	chr4:95856600-95858400	Enhancers	Muscle Satellite Cultured Cells	--
9	chr4:95856800-95861200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr4:95857000-95860600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr4:95857000-95860800	Weak transcription	Osteobl	bone
12	chr4:95857400-95858200	Enhancers	Stomach Smooth Muscle	stomach
13	chr4:95857400-95861200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr4:95857800-95858600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr4:95858000-95858400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr4:95858000-95858600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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