Variant report

Variant	rs35946366
Chromosome Location	chr4:62702002-62702003
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 57 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10000772	0.84[ASN][1000 genomes]
rs10004644	0.92[EUR][1000 genomes]
rs10021525	0.91[EUR][1000 genomes]
rs10021694	0.91[EUR][1000 genomes]
rs11734607	1.00[ASN][1000 genomes]
rs12509742	0.88[ASN][1000 genomes]
rs12641643	0.92[EUR][1000 genomes]
rs12651006	0.92[EUR][1000 genomes]
rs1551096	0.92[EUR][1000 genomes]
rs17090543	0.98[ASN][1000 genomes]
rs17292058	0.81[EUR][1000 genomes]
rs1817052	0.93[ASN][1000 genomes]
rs1839614	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1868789	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1868790	1.00[ASN][1000 genomes]
rs1901222	1.00[ASN][1000 genomes]
rs1901223	0.87[ASN][1000 genomes]
rs2013374	0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2122641	0.93[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2122642	0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2167280	0.88[ASN][1000 genomes]
rs2198056	0.98[ASN][1000 genomes]
rs2345041	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs28421285	0.81[EUR][1000 genomes]
rs28534995	0.98[ASN][1000 genomes]
rs28587627	0.84[ASN][1000 genomes]
rs2881027	0.98[ASN][1000 genomes]
rs34637663	1.00[ASN][1000 genomes]
rs34764145	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs34907045	0.98[ASN][1000 genomes]
rs3860623	0.84[EUR][1000 genomes]
rs4467601	0.96[ASN][1000 genomes]
rs4487384	0.84[ASN][1000 genomes]
rs4860434	0.88[ASN][1000 genomes]
rs4860436	0.93[EUR][1000 genomes]
rs62304373	0.98[ASN][1000 genomes]
rs6551658	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6551659	0.93[EUR][1000 genomes]
rs6551660	0.92[EUR][1000 genomes]
rs6551662	0.85[EUR][1000 genomes]
rs6832443	0.92[EUR][1000 genomes]
rs6845019	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6855424	0.84[ASN][1000 genomes]
rs7437698	0.92[EUR][1000 genomes]
rs7665141	0.93[EUR][1000 genomes]
rs7676289	0.88[ASN][1000 genomes]
rs7679793	0.98[ASN][1000 genomes]
rs7695134	0.93[EUR][1000 genomes]
rs9790538	1.00[ASN][1000 genomes]
rs9884313	0.99[ASN][1000 genomes]
rs990640	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9942184	0.99[ASN][1000 genomes]
rs9990553	0.91[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	nsv461377	chr4:62368762-62883431	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv594328	chr4:62368762-62883431	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv829949	chr4:62615637-62761629	Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv428760	chr4:62649399-62824542	Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:62695000-62704000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr4:62698000-62703600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr4:62700200-62702400	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr4:62700200-62704200	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr4:62700400-62703000	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr4:62700400-62704200	Enhancers	HUES6 Cell Line	embryonic stem cell
7	chr4:62700400-62704800	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr4:62700800-62702600	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr4:62701600-62702200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr4:62701600-62703600	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr4:62701800-62703000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr4:62701800-62703200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr4:62701800-62707000	Weak transcription	H1 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links