Variant report

Variant	rs6806589
Chromosome Location	chr3:76148360-76148361
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 61 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs10511039	0.83[ASN][1000 genomes]
rs12714848	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1489090	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1489091	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1489092	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1489093	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1489096	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1489097	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1489098	0.83[AMR][1000 genomes]
rs1489099	0.82[AMR][1000 genomes]
rs1903731	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1968951	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2126537	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2171638	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2324470	0.83[AMR][1000 genomes]
rs2324471	0.83[AMR][1000 genomes]
rs4260451	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4306863	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4449327	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4484199	0.81[AMR][1000 genomes]
rs4566540	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs4624567	0.82[AMR][1000 genomes]
rs4855969	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6549831	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs6549832	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6770732	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6776686	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6776915	0.83[AMR][1000 genomes]
rs6778177	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6778933	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6779552	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6780479	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6780798	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6782618	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6786288	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6788637	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6802647	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7620001	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7632524	0.82[ASN][1000 genomes]
rs7643807	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7653310	0.83[AMR][1000 genomes]
rs9754680	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9755934	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9755939	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9815472	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9815982	0.87[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs9824924	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs9833153	0.84[EUR][1000 genomes]
rs9840618	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9841567	0.92[ASN][1000 genomes]
rs9852030	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs9853890	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9879542	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1012705	chr3:76047819-76276542	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv998038	chr3:76053664-76218646	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv536591	chr3:76053664-76218646	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv1007586	chr3:76053664-76280612	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv999868	chr3:76068393-76274977	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
6	esv2757876	chr3:76077290-76167295	Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv1004976	chr3:76098108-76218646	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	n/a	n/a	inside rSNPs	diseases
8	nsv963334	chr3:76144827-76201280	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs6806589	RYBP	cis	cerebellum	SCAN
rs6806589	EBLN2	cis	cerebellum	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:76143800-76148400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr3:76147600-76148400	Weak transcription	HUES48 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links