Variant report

Variant	rs62308210
Chromosome Location	chr4:94019322-94019323
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs10011751	0.90[ASN][1000 genomes]
rs11724865	0.92[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs11725186	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11730324	0.82[ASN][1000 genomes]
rs11733088	0.92[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs12108474	0.97[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs13105522	0.92[ASN][1000 genomes]
rs1847262	0.92[ASN][1000 genomes]
rs28513308	0.92[AMR][1000 genomes]
rs34829716	0.92[ASN][1000 genomes]
rs35764687	0.92[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs4373126	0.92[ASN][1000 genomes]
rs56011292	0.92[ASN][1000 genomes]
rs58129862	0.84[ASN][1000 genomes]
rs59397055	0.87[ASN][1000 genomes]
rs62308172	0.82[ASN][1000 genomes]
rs62308200	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs62308201	0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs62308202	0.92[ASN][1000 genomes]
rs62308203	0.92[EUR][1000 genomes]
rs62308204	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs62308207	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs62308209	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs62308212	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs62308213	0.84[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs62308214	0.90[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs6849575	0.92[ASN][1000 genomes]
rs72665250	0.92[ASN][1000 genomes]
rs72665251	0.92[ASN][1000 genomes]
rs72665274	0.92[ASN][1000 genomes]
rs72665276	0.92[ASN][1000 genomes]
rs72887689	0.84[ASN][1000 genomes]
rs72887690	0.84[ASN][1000 genomes]
rs72887694	0.84[ASN][1000 genomes]
rs72887698	0.92[AMR][1000 genomes]
rs72889639	0.92[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs72889671	0.85[AMR][1000 genomes]

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	nsv1007177	chr4:93834536-94155349	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv537186	chr4:93834536-94155349	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv931937	chr4:93869856-94155348	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv1011740	chr4:93904073-94073963	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
5	esv3374790	chr4:93959718-94063251	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv999660	chr4:93982635-94107714	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
7	esv3444894	chr4:94019290-94019464	Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:94008000-94037400	Weak transcription	HUES48 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links