Variant report

Variant	rs769079
Chromosome Location	chr2:149319042-149319043
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 50 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs10165986	0.95[ASN][1000 genomes]
rs10171728	0.92[ASN][1000 genomes]
rs10177983	1.00[CHB][hapmap];0.92[JPT][hapmap];0.86[ASN][1000 genomes]
rs10181555	1.00[CHB][hapmap];0.92[JPT][hapmap];0.89[ASN][1000 genomes]
rs10181614	1.00[CHB][hapmap];0.92[JPT][hapmap];0.86[ASN][1000 genomes]
rs10190474	0.97[ASN][1000 genomes]
rs10200061	0.93[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs10204718	0.86[ASN][1000 genomes]
rs10497035	0.98[ASN][1000 genomes]
rs10928401	0.98[ASN][1000 genomes]
rs10928402	0.98[ASN][1000 genomes]
rs10928408	1.00[CHB][hapmap];0.92[JPT][hapmap];0.92[ASN][1000 genomes]
rs11687034	1.00[CHB][hapmap];0.92[JPT][hapmap];0.86[ASN][1000 genomes]
rs11687783	0.89[ASN][1000 genomes]
rs11688979	1.00[CHB][hapmap];1.00[CHD][hapmap];0.84[GIH][hapmap];0.85[JPT][hapmap];0.80[MEX][hapmap];0.85[ASN][1000 genomes]
rs12691801	1.00[ASN][1000 genomes]
rs13016446	1.00[CHB][hapmap];0.92[JPT][hapmap];0.89[ASN][1000 genomes]
rs13407240	0.85[ASN][1000 genomes]
rs13427633	1.00[ASN][1000 genomes]
rs16828908	1.00[ASN][1000 genomes]
rs16828910	0.82[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs2382230	0.98[ASN][1000 genomes]
rs28533220	0.89[ASN][1000 genomes]
rs3936439	0.98[ASN][1000 genomes]
rs4450539	0.92[ASN][1000 genomes]
rs4624325	0.89[ASN][1000 genomes]
rs4972282	0.83[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs4972374	1.00[ASN][1000 genomes]
rs6430322	0.93[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs6430324	0.86[AFR][1000 genomes]
rs6430326	1.00[ASN][1000 genomes]
rs6716704	1.00[CHB][hapmap];1.00[CHD][hapmap];0.84[GIH][hapmap];0.92[JPT][hapmap];0.80[MEX][hapmap];0.86[ASN][1000 genomes]
rs6736226	0.93[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs6736270	1.00[ASN][1000 genomes]
rs6736369	1.00[ASN][1000 genomes]
rs6739607	0.93[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs6747262	1.00[ASN][1000 genomes]
rs6750878	0.93[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs7574168	1.00[CHB][hapmap];0.92[JPT][hapmap];0.86[ASN][1000 genomes]
rs7574666	1.00[CHB][hapmap];1.00[CHD][hapmap];0.82[GIH][hapmap];1.00[JPT][hapmap];0.80[MEX][hapmap];0.86[ASN][1000 genomes]
rs921242	1.00[ASN][1000 genomes]
rs921243	1.00[ASN][1000 genomes]
rs9636222	1.00[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	esv2751831	chr2:149151358-150105603	Weak transcription Flanking Bivalent TSS/Enh Strong transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
2	nsv1000101	chr2:149165813-149361220	Enhancers Strong transcription Genic enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv868861	chr2:149198443-149434604	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
4	nsv917109	chr2:149198443-149948302	ZNF genes & repeats Weak transcription Flanking Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
5	nsv1004663	chr2:149214090-149373061	Enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	esv2762913	chr2:149249683-149345487	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	nsv527539	chr2:149283070-149330251	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	Chromatin interactive region	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	chr2:149312600-149319400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr2:149317200-149319800	Enhancers	Fetal Lung	lung
3	chr2:149317400-149319200	Enhancers	Placenta	Placenta
4	chr2:149318000-149320200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr2:149318200-149319600	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr2:149318400-149319200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr2:149318800-149319400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr2:149318800-149319400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr2:149318800-149319400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr2:149318800-149319600	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr2:149318800-149319600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr2:149319000-149319400	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr2:149319000-149319400	Active TSS	K562	blood

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