Variant report

Variant	rs35254904
Chromosome Location	chr4:95858762-95858763
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 64 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:57)

rs_ID	r²[population]
rs10516956	0.97[ASN][1000 genomes]
rs11722010	0.85[ASN][1000 genomes]
rs11934132	0.97[ASN][1000 genomes]
rs11946254	0.90[ASN][1000 genomes]
rs12505736	0.90[ASN][1000 genomes]
rs12505819	0.85[ASN][1000 genomes]
rs12513378	0.90[ASN][1000 genomes]
rs12640910	0.93[ASN][1000 genomes]
rs12642960	0.88[ASN][1000 genomes]
rs12643902	0.88[ASN][1000 genomes]
rs13103598	0.88[ASN][1000 genomes]
rs13106009	0.85[ASN][1000 genomes]
rs13110508	0.88[ASN][1000 genomes]
rs13118309	0.90[ASN][1000 genomes]
rs13127704	0.88[ASN][1000 genomes]
rs13143626	0.90[ASN][1000 genomes]
rs13144086	0.88[ASN][1000 genomes]
rs13149539	0.90[ASN][1000 genomes]
rs1373648	0.83[ASN][1000 genomes]
rs1373649	0.85[ASN][1000 genomes]
rs1373651	0.86[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs1444924	0.97[ASN][1000 genomes]
rs1444925	0.90[ASN][1000 genomes]
rs1444927	0.90[ASN][1000 genomes]
rs1444928	0.96[ASN][1000 genomes]
rs17401411	0.88[ASN][1000 genomes]
rs17401571	0.88[ASN][1000 genomes]
rs1992650	0.88[ASN][1000 genomes]
rs1992651	0.88[ASN][1000 genomes]
rs2120835	0.81[ASN][1000 genomes]
rs34340033	0.88[ASN][1000 genomes]
rs3775030	0.81[ASN][1000 genomes]
rs3796410	0.81[ASN][1000 genomes]
rs3796411	0.96[ASN][1000 genomes]
rs3796413	0.88[ASN][1000 genomes]
rs3796417	0.90[ASN][1000 genomes]
rs3796418	0.90[ASN][1000 genomes]
rs3796419	0.90[ASN][1000 genomes]
rs3796422	0.90[ASN][1000 genomes]
rs3796423	0.90[ASN][1000 genomes]
rs3796424	0.88[ASN][1000 genomes]
rs3796425	0.90[ASN][1000 genomes]
rs3821963	0.98[ASN][1000 genomes]
rs62316224	0.88[ASN][1000 genomes]
rs6823752	0.97[ASN][1000 genomes]
rs7655484	0.86[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs7658478	0.90[ASN][1000 genomes]
rs7661049	0.97[ASN][1000 genomes]
rs7671870	0.90[ASN][1000 genomes]
rs7673752	0.90[ASN][1000 genomes]
rs7673943	0.90[ASN][1000 genomes]
rs7691748	0.88[ASN][1000 genomes]
rs7699472	0.90[ASN][1000 genomes]
rs930581	0.88[ASN][1000 genomes]
rs9307150	0.88[ASN][1000 genomes]
rs9684200	0.88[ASN][1000 genomes]
rs9684808	0.88[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:12 , 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	chr4:95856000-95860800	Weak transcription	HUVEC	blood vessel
5	chr4:95856800-95861200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr4:95857000-95860600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr4:95857000-95860800	Weak transcription	Osteobl	bone
8	chr4:95857400-95861200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr4:95858400-95860200	Weak transcription	Muscle Satellite Cultured Cells	--
10	chr4:95858600-95858800	Enhancers	A549	lung
11	chr4:95858600-95860800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr4:95858600-95861400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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