Variant report

Variant	rs7630937
Chromosome Location	chr3:76126167-76126168
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 55 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs11922976	0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11923013	0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12714847	0.94[ASN][1000 genomes]
rs1489090	0.96[ASN][1000 genomes]
rs1489091	0.96[ASN][1000 genomes]
rs1489092	0.96[ASN][1000 genomes]
rs1489093	0.95[ASN][1000 genomes]
rs1489096	0.96[ASN][1000 genomes]
rs1489097	0.95[ASN][1000 genomes]
rs1489098	0.96[ASN][1000 genomes]
rs1968951	0.96[ASN][1000 genomes]
rs2324470	0.95[ASN][1000 genomes]
rs2324471	0.96[ASN][1000 genomes]
rs4260451	0.96[ASN][1000 genomes]
rs4306863	0.96[ASN][1000 genomes]
rs4566540	0.96[ASN][1000 genomes]
rs4855969	0.99[ASN][1000 genomes]
rs57114044	0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6549832	0.96[ASN][1000 genomes]
rs6776686	0.95[ASN][1000 genomes]
rs6778177	0.96[ASN][1000 genomes]
rs6778933	0.99[ASN][1000 genomes]
rs6779552	0.99[ASN][1000 genomes]
rs6780227	0.93[ASN][1000 genomes]
rs6780479	0.95[ASN][1000 genomes]
rs6780798	0.96[ASN][1000 genomes]
rs6783384	0.96[ASN][1000 genomes]
rs6802647	0.99[ASN][1000 genomes]
rs7620001	0.88[ASN][1000 genomes]
rs7625148	0.84[ASN][1000 genomes]
rs7631220	0.84[AFR][1000 genomes];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7642285	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7642499	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7653310	0.96[ASN][1000 genomes]
rs9754680	0.98[ASN][1000 genomes]
rs9755934	0.98[ASN][1000 genomes]
rs9755939	0.98[ASN][1000 genomes]
rs9812834	0.94[ASN][1000 genomes]
rs9824924	0.95[ASN][1000 genomes]
rs9833136	0.96[ASN][1000 genomes]
rs9833153	0.96[ASN][1000 genomes]
rs9840618	0.99[ASN][1000 genomes]
rs9841567	0.84[EUR][1000 genomes]
rs9853890	0.99[ASN][1000 genomes]
rs9879542	0.95[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 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	nsv979847	chr3:76058868-76143057	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
6	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
7	nsv869827	chr3:76074846-76142916	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
8	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
9	nsv876996	chr3:76094221-76131251	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
10	nsv1004976	chr3:76098108-76218646	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	n/a	n/a	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs7630937	EBLN2	cis	cerebellum	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:76116600-76129400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links