Variant report

Variant	rs12136023
Chromosome Location	chr1:86340262-86340263
allele	A/C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 78 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:71)

rs_ID	r²[population]
rs1010058	0.81[EUR][1000 genomes]
rs10873725	0.81[EUR][1000 genomes]
rs11161686	0.81[EUR][1000 genomes]
rs11161687	0.81[EUR][1000 genomes]
rs11161689	0.96[ASN][1000 genomes]
rs11161691	0.96[ASN][1000 genomes]
rs11161692	0.96[ASN][1000 genomes]
rs11161694	0.96[ASN][1000 genomes]
rs11161698	0.96[ASN][1000 genomes]
rs12091504	0.96[ASN][1000 genomes]
rs12119433	1.00[JPT][hapmap]
rs12122234	1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12130385	1.00[JPT][hapmap]
rs12138101	1.00[JPT][hapmap]
rs12240129	0.96[ASN][1000 genomes]
rs12723176	0.96[ASN][1000 genomes]
rs12725203	0.96[ASN][1000 genomes]
rs12725350	0.96[ASN][1000 genomes]
rs12726975	0.96[ASN][1000 genomes]
rs12727503	0.96[ASN][1000 genomes]
rs12731603	0.96[ASN][1000 genomes]
rs12734458	0.96[ASN][1000 genomes]
rs12735496	0.96[ASN][1000 genomes]
rs12736249	0.96[ASN][1000 genomes]
rs12739200	0.96[ASN][1000 genomes]
rs12739425	0.96[ASN][1000 genomes]
rs12739620	0.96[ASN][1000 genomes]
rs12740060	0.96[ASN][1000 genomes]
rs12740827	0.96[ASN][1000 genomes]
rs12740836	0.96[ASN][1000 genomes]
rs12742187	0.85[ASN][1000 genomes]
rs12745489	0.96[ASN][1000 genomes]
rs12746617	0.96[ASN][1000 genomes]
rs12747217	0.96[ASN][1000 genomes]
rs12747420	0.96[ASN][1000 genomes]
rs12749558	0.92[ASN][1000 genomes]
rs12751341	0.96[ASN][1000 genomes]
rs12752474	0.96[ASN][1000 genomes]
rs12753255	0.96[ASN][1000 genomes]
rs12755099	0.96[ASN][1000 genomes]
rs12755570	0.96[ASN][1000 genomes]
rs12757388	0.96[ASN][1000 genomes]
rs12759687	0.96[ASN][1000 genomes]
rs1325260	0.81[EUR][1000 genomes]
rs1564515	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1564517	0.92[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1604567	0.96[ASN][1000 genomes]
rs1962482	1.00[JPT][hapmap]
rs2046158	1.00[JPT][hapmap]
rs2046159	1.00[JPT][hapmap]
rs2086495	0.96[ASN][1000 genomes]
rs2170331	0.92[ASN][1000 genomes]
rs2297744	0.81[EUR][1000 genomes]
rs28415684	0.96[ASN][1000 genomes]
rs28571037	0.96[ASN][1000 genomes]
rs34503069	0.84[ASN][1000 genomes]
rs34589269	0.85[ASN][1000 genomes]
rs35545564	0.96[ASN][1000 genomes]
rs35826410	0.96[ASN][1000 genomes]
rs4912437	0.80[EUR][1000 genomes]
rs4912446	0.81[EUR][1000 genomes]
rs6657706	0.92[ASN][1000 genomes]
rs6665006	0.96[ASN][1000 genomes]
rs6666627	0.92[ASN][1000 genomes]
rs67487620	0.96[ASN][1000 genomes]
rs71078626	0.81[ASN][1000 genomes]
rs7520948	0.96[ASN][1000 genomes]
rs7523196	0.96[ASN][1000 genomes]
rs7530839	0.88[ASN][1000 genomes]
rs7539765	0.96[ASN][1000 genomes]
rs7554796	0.96[ASN][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	nsv817212	chr1:86127851-86658426	Enhancers Weak transcription Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv546721	chr1:86226352-86392577	Weak transcription Strong transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
3	nsv999743	chr1:86241246-86364846	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
4	nsv1011293	chr1:86270649-86416972	Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
5	nsv546722	chr1:86278315-86891073	Enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	9 gene(s)	inside rSNPs	diseases
6	nsv871189	chr1:86315724-86402244	Weak transcription Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
7	esv1810714	chr1:86339811-86392577	Weak transcription Enhancers ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:86331400-86341600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr1:86333200-86343800	Weak transcription	GM12878-XiMat	blood
3	chr1:86339200-86341200	Strong transcription	Fetal Lung	lung
4	chr1:86339400-86342600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr1:86339600-86342400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr1:86339800-86341200	Strong transcription	Primary hematopoietic stem cells	blood
7	chr1:86339800-86342400	Strong transcription	Primary hematopoietic stem cells short term culture	blood

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