Variant report

Variant	rs1420835
Chromosome Location	chr8:5149892-5149893
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 90 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:82)

rs_ID	r²[population]
rs10100035	0.91[AFR][1000 genomes];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10100174	0.91[AFR][1000 genomes];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10100197	0.91[AFR][1000 genomes];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10104304	0.93[ASN][1000 genomes]
rs10107440	0.98[ASN][1000 genomes]
rs11136851	0.94[ASN][1000 genomes]
rs11780928	0.93[ASN][1000 genomes]
rs11782726	0.98[ASN][1000 genomes]
rs11782756	0.93[ASN][1000 genomes]
rs11783530	0.94[ASN][1000 genomes]
rs11787485	0.91[ASN][1000 genomes]
rs11989368	0.82[ASN][1000 genomes]
rs11990192	0.85[EUR][1000 genomes]
rs12546222	0.91[AFR][1000 genomes];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12548405	0.98[ASN][1000 genomes]
rs12549479	0.82[ASN][1000 genomes]
rs12678557	0.93[AFR][1000 genomes];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12678576	0.92[AFR][1000 genomes];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12679623	0.94[ASN][1000 genomes]
rs12679657	0.94[ASN][1000 genomes]
rs12681537	0.93[ASN][1000 genomes]
rs12716627	0.99[ASN][1000 genomes]
rs12716628	0.99[ASN][1000 genomes]
rs12716629	0.88[ASN][1000 genomes]
rs12716630	0.91[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs12716631	0.93[AFR][1000 genomes];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13249114	0.91[ASN][1000 genomes]
rs13249604	0.91[ASN][1000 genomes]
rs13251656	0.93[ASN][1000 genomes]
rs13275405	0.93[ASN][1000 genomes]
rs13276499	0.93[ASN][1000 genomes]
rs1362681	0.92[AFR][1000 genomes];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1420836	1.00[ASN][1000 genomes]
rs1420837	0.91[AFR][1000 genomes];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1420838	0.99[ASN][1000 genomes]
rs1420839	0.98[ASN][1000 genomes]
rs1420840	0.98[ASN][1000 genomes]
rs1420841	0.98[ASN][1000 genomes]
rs17351612	0.85[EUR][1000 genomes]
rs17351653	0.85[EUR][1000 genomes]
rs17436160	0.85[EUR][1000 genomes]
rs2111420	0.94[ASN][1000 genomes]
rs2111421	0.94[ASN][1000 genomes]
rs2193429	0.93[ASN][1000 genomes]
rs2216312	0.93[ASN][1000 genomes]
rs2407956	0.93[ASN][1000 genomes]
rs2407957	0.93[ASN][1000 genomes]
rs2407958	0.94[ASN][1000 genomes]
rs2407960	0.94[ASN][1000 genomes]
rs4270986	0.94[ASN][1000 genomes]
rs4369005	0.94[ASN][1000 genomes]
rs4375025	0.94[ASN][1000 genomes]
rs4386997	0.82[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs4449817	0.94[ASN][1000 genomes]
rs4552921	0.94[ASN][1000 genomes]
rs4552922	0.94[ASN][1000 genomes]
rs4552923	0.94[ASN][1000 genomes]
rs4598272	0.94[ASN][1000 genomes]
rs4875492	0.94[ASN][1000 genomes]
rs4875493	0.94[ASN][1000 genomes]
rs4875494	0.94[ASN][1000 genomes]
rs62493298	0.93[ASN][1000 genomes]
rs62493299	0.91[ASN][1000 genomes]
rs6990899	0.98[ASN][1000 genomes]
rs6991097	0.85[EUR][1000 genomes]
rs6994845	0.98[ASN][1000 genomes]
rs6995158	0.92[AFR][1000 genomes];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7014631	1.00[ASN][1000 genomes]
rs7815253	0.93[AFR][1000 genomes];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7823730	0.94[ASN][1000 genomes]
rs888252	0.98[ASN][1000 genomes]
rs9657410	0.92[AFR][1000 genomes];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9657412	0.92[AFR][1000 genomes];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9657413	0.92[AFR][1000 genomes];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9657414	0.93[AFR][1000 genomes];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs966354	0.94[ASN][1000 genomes]
rs966355	0.94[ASN][1000 genomes]
rs966356	0.94[ASN][1000 genomes]
rs985109	0.93[AFR][1000 genomes];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs985110	0.96[ASN][1000 genomes]
rs985111	0.88[AFR][1000 genomes];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs985112	0.92[AFR][1000 genomes];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][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	nsv498130	chr8:4532988-5176376	Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Weak transcription Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv889978	chr8:4853197-5460166	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv831217	chr8:5007449-5210093	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv609902	chr8:5088786-5533605	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv889982	chr8:5119564-5150113	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases
6	nsv889983	chr8:5119564-5154026	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
7	nsv889984	chr8:5119564-5157363	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases
8	nsv1031427	chr8:5129076-5603378	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:5148800-5150000	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr8:5149600-5150200	Enhancers	HUES64 Cell Line	embryonic stem cell
3	chr8:5149800-5150400	Enhancers	HUES48 Cell Line	embryonic stem cell

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