Variant report

Variant	rs7698964
Chromosome Location	chr4:95856974-95856975
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 49 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs10488912	0.86[CEU][hapmap]
rs11097447	1.00[CEU][hapmap];0.86[EUR][1000 genomes]
rs11097448	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11930676	0.89[EUR][1000 genomes]
rs11932930	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11939949	1.00[CEU][hapmap];0.89[EUR][1000 genomes]
rs11944292	0.85[CEU][hapmap]
rs11945215	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11946484	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12501965	1.00[JPT][hapmap]
rs12510047	0.86[CEU][hapmap]
rs12511697	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12511896	0.85[CEU][hapmap]
rs12511962	0.86[CEU][hapmap]
rs12512679	0.86[CEU][hapmap]
rs1348606	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17401285	0.86[CEU][hapmap]
rs17428494	0.85[CEU][hapmap]
rs17428501	0.85[CEU][hapmap]
rs17428550	0.80[CEU][hapmap]
rs17428564	0.85[CEU][hapmap]
rs17428830	0.86[CEU][hapmap]
rs17429175	0.86[CEU][hapmap]
rs17500351	0.86[CEU][hapmap]
rs17500892	0.85[CEU][hapmap]
rs17500926	0.86[CEU][hapmap]
rs17501107	0.85[CEU][hapmap]
rs2023836	0.86[CEU][hapmap]
rs2865411	0.86[CEU][hapmap]
rs4455423	1.00[JPT][hapmap]
rs4623010	0.86[CEU][hapmap]
rs58221294	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58250445	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs59346137	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59753663	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs60017378	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73838611	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs73838612	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs73838615	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7684060	1.00[JPT][hapmap]
rs7699554	0.85[CEU][hapmap]
rs916875	0.86[CEU][hapmap]

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:18 , 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	chr4:95853600-95857800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr4:95855400-95857000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr4:95855600-95858000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr4:95855800-95857000	Enhancers	Osteobl	bone
9	chr4:95855800-95858000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr4:95856000-95860800	Weak transcription	HUVEC	blood vessel
11	chr4:95856200-95857000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr4:95856400-95857600	Enhancers	Aorta	Aorta
13	chr4:95856400-95858200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr4:95856400-95858600	Flanking Active TSS	A549	lung
15	chr4:95856600-95858400	Enhancers	Muscle Satellite Cultured Cells	--
16	chr4:95856800-95857000	Enhancers	Placenta Amnion	Placenta Amnion
17	chr4:95856800-95857200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr4:95856800-95861200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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