Variant report

Variant	rs4694490
Chromosome Location	chr4:69859702-69859703
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 88 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:79)

rs_ID	r²[population]
rs10006595	0.84[EUR][1000 genomes]
rs10019619	0.98[EUR][1000 genomes]
rs10027817	0.83[EUR][1000 genomes]
rs10030220	0.89[EUR][1000 genomes]
rs11249517	0.83[EUR][1000 genomes]
rs11249518	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11249520	0.91[EUR][1000 genomes]
rs11725519	0.89[EUR][1000 genomes]
rs12501837	0.86[EUR][1000 genomes]
rs12505263	0.82[EUR][1000 genomes]
rs12509175	0.89[EUR][1000 genomes]
rs12512098	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12719832	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12719833	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12719834	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12719835	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs13102620	0.88[EUR][1000 genomes]
rs13108709	0.88[EUR][1000 genomes]
rs13116752	0.86[EUR][1000 genomes]
rs13127081	0.91[EUR][1000 genomes]
rs13128177	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13140844	0.91[TSI][hapmap];0.86[EUR][1000 genomes]
rs13145165	0.98[EUR][1000 genomes]
rs13145304	0.88[EUR][1000 genomes]
rs13147569	0.86[EUR][1000 genomes]
rs13147648	0.91[TSI][hapmap];0.88[EUR][1000 genomes]
rs1458229	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1458230	0.84[EUR][1000 genomes]
rs1598903	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1841055	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1902923	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1902936	0.83[EUR][1000 genomes]
rs1962952	0.83[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs2011000	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2013866	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2199039	0.82[EUR][1000 genomes]
rs2199040	0.83[EUR][1000 genomes]
rs2331627	0.98[EUR][1000 genomes]
rs28386872	0.87[EUR][1000 genomes]
rs28485675	0.84[EUR][1000 genomes]
rs3886642	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs3886643	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs4088518	0.94[ASN][1000 genomes]
rs4146121	0.83[EUR][1000 genomes]
rs4235106	1.00[CEU][hapmap];0.91[EUR][1000 genomes]
rs4235108	0.91[TSI][hapmap];0.89[EUR][1000 genomes]
rs4235111	0.86[EUR][1000 genomes]
rs4235112	0.86[EUR][1000 genomes]
rs4299665	0.86[EUR][1000 genomes]
rs4299666	0.91[TSI][hapmap];0.86[EUR][1000 genomes]
rs4304032	0.91[EUR][1000 genomes]
rs4305590	0.91[TSI][hapmap];0.89[EUR][1000 genomes]
rs4312824	0.86[EUR][1000 genomes]
rs4353969	0.88[EUR][1000 genomes]
rs4365792	0.86[EUR][1000 genomes]
rs4440295	0.93[CEU][hapmap];0.85[GIH][hapmap];0.91[TSI][hapmap];0.88[EUR][1000 genomes]
rs4487432	0.83[EUR][1000 genomes]
rs4495114	0.88[EUR][1000 genomes]
rs4591680	0.86[EUR][1000 genomes]
rs4694491	0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4694551	0.87[EUR][1000 genomes]
rs6812186	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6812415	0.85[EUR][1000 genomes]
rs6827511	0.91[TSI][hapmap];0.89[EUR][1000 genomes]
rs6828317	0.87[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs6831147	0.95[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6837000	0.95[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6839405	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6843788	0.87[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs6847948	0.85[EUR][1000 genomes]
rs7441736	0.89[EUR][1000 genomes]
rs7673174	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7679122	0.80[EUR][1000 genomes]
rs7690181	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7691258	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7691445	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7695476	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs988887	0.84[EUR][1000 genomes]
rs9998014	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1005513	chr4:69446718-69890307	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
2	nsv999654	chr4:69661415-70132110	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
3	esv3420586	chr4:69680878-70322918	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
4	nsv1067773	chr4:69718248-70715727	ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
5	esv3468151	chr4:69718675-70322776	Enhancers Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
6	esv3468153	chr4:69718675-70322776	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
7	nsv967758	chr4:69780530-69870183	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
8	nsv829962	chr4:69786869-69910283	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
9	nsv594582	chr4:69827340-69988378	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:69858800-69860000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links