Variant report

Variant	rs7684060
Chromosome Location	chr4:95699398-95699399
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:95689034..95690776-chr4:95698593..95701068,2	K562	blood:

Extended variants
information (count: 58 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:54)

rs_ID	r²[population]
rs10516954	0.87[CEU][hapmap];0.89[EUR][1000 genomes]
rs11929751	0.86[CEU][hapmap];0.91[EUR][1000 genomes]
rs11932119	1.00[YRI][hapmap];0.83[AFR][1000 genomes]
rs11943082	0.86[CEU][hapmap];0.91[EUR][1000 genomes]
rs12501965	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13106939	0.87[EUR][1000 genomes]
rs13113279	1.00[ASN][1000 genomes]
rs13130042	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs13138560	0.89[EUR][1000 genomes]
rs13140820	0.89[EUR][1000 genomes]
rs13141292	0.89[EUR][1000 genomes]
rs13141832	0.86[AFR][1000 genomes];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13146661	0.89[EUR][1000 genomes]
rs13149911	0.86[CEU][hapmap];0.89[EUR][1000 genomes]
rs1348606	1.00[JPT][hapmap]
rs1472964	0.87[CEU][hapmap];0.91[EUR][1000 genomes]
rs1509619	0.91[CEU][hapmap];0.87[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs17022181	0.92[EUR][1000 genomes]
rs17022183	0.91[CEU][hapmap];0.81[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs17022258	0.95[CEU][hapmap]
rs28427211	0.91[EUR][1000 genomes]
rs34051091	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34618938	0.88[EUR][1000 genomes]
rs34752274	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs35070714	0.91[EUR][1000 genomes]
rs35271777	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs35288991	0.89[EUR][1000 genomes]
rs35501794	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs35575650	0.85[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35627971	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs35965331	0.89[EUR][1000 genomes]
rs35966527	1.00[ASN][1000 genomes]
rs4374630	1.00[CHB][hapmap]
rs4455423	1.00[JPT][hapmap]
rs60213345	1.00[ASN][1000 genomes]
rs62316513	0.92[EUR][1000 genomes]
rs6532507	0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6817189	0.81[AFR][1000 genomes]
rs6819188	0.82[CEU][hapmap]
rs6837341	0.92[EUR][1000 genomes]
rs6838436	0.92[EUR][1000 genomes]
rs6842692	0.82[YRI][hapmap]
rs7667095	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7667584	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7677261	0.86[CEU][hapmap];0.89[EUR][1000 genomes]
rs7677422	0.89[EUR][1000 genomes]
rs7693277	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7698964	1.00[JPT][hapmap]
rs925282	0.91[CEU][hapmap];0.85[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs925283	0.91[CEU][hapmap];0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs9307147	1.00[YRI][hapmap];0.83[AFR][1000 genomes]
rs955735	0.89[EUR][1000 genomes]
rs997902	0.87[CEU][hapmap];0.89[EUR][1000 genomes]
rs997903	0.89[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 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

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:95683000-95703600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr4:95698400-95699800	Weak transcription	A549	lung

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