Variant report

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10514856	0.95[CEU][hapmap];0.86[EUR][1000 genomes]
rs10514881	0.83[AMR][1000 genomes]
rs10940647	0.88[EUR][1000 genomes]
rs10940648	0.94[CEU][hapmap];0.89[EUR][1000 genomes]
rs11738448	0.85[CEU][hapmap];0.84[AMR][1000 genomes]
rs11741470	0.94[CEU][hapmap];0.85[EUR][1000 genomes]
rs11747378	1.00[CEU][hapmap];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs13164391	0.82[EUR][1000 genomes]
rs13168643	1.00[CEU][hapmap];0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs13177163	0.94[CEU][hapmap];0.82[EUR][1000 genomes]
rs13186779	0.82[EUR][1000 genomes]
rs1504985	0.85[CEU][hapmap];0.84[AMR][1000 genomes]
rs2938782	1.00[CEU][hapmap];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs2938787	0.89[CEU][hapmap];0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2963820	0.95[CEU][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2963823	1.00[CEU][hapmap];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs298056	0.84[CEU][hapmap]
rs298069	0.84[CEU][hapmap]
rs298087	0.82[EUR][1000 genomes]
rs3111174	0.83[CEU][hapmap];0.84[AMR][1000 genomes]
rs35302677	0.82[EUR][1000 genomes]
rs35339176	0.82[EUR][1000 genomes]
rs35526661	0.86[EUR][1000 genomes]
rs59251157	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs62370530	0.83[EUR][1000 genomes]
rs877744	0.94[CEU][hapmap];0.89[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1018015	chr5:58889470-59532667	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
2	nsv537766	chr5:58889470-59532667	Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
3	nsv534614	chr5:58962510-59388525	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	12 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	chr5:59087400-59106000	Weak transcription	Aorta	Aorta
2	chr5:59095400-59097800	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr5:59096000-59098000	Enhancers	Hela-S3	cervix
4	chr5:59096000-59101400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr5:59096400-59106000	Weak transcription	Fetal Brain Male	brain
6	chr5:59096800-59097800	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr5:59096800-59101800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr5:59097200-59098200	Enhancers	Fetal Lung	lung
9	chr5:59097400-59097800	Bivalent Enhancer	HUVEC	blood vessel
10	chr5:59097400-59098000	Enhancers	A549	lung

Quick Search: