Variant report

Variant	rs11690292
Chromosome Location	chr2:40455984-40455985
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs10490208	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11674102	0.81[CHB][hapmap];0.89[JPT][hapmap]
rs11682111	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11682470	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11691096	0.84[AMR][1000 genomes]
rs12104840	0.93[CHB][hapmap]
rs12474968	0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1428579	0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs17504446	0.81[CHB][hapmap];0.89[JPT][hapmap];0.83[AMR][1000 genomes]
rs17504670	0.88[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1985526	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2540904	0.80[CEU][hapmap]
rs35113834	0.87[AFR][1000 genomes];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs371492	0.81[CEU][hapmap]
rs404226	0.82[CEU][hapmap]
rs4581943	0.88[CHB][hapmap];0.85[JPT][hapmap]
rs4952401	0.88[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4952591	0.83[JPT][hapmap]
rs4952594	0.96[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.85[YRI][hapmap];0.89[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4952599	0.87[CHB][hapmap];0.84[JPT][hapmap]
rs6736607	0.92[ASN][1000 genomes]
rs7588446	0.92[ASN][1000 genomes]
rs7602176	0.87[CHB][hapmap];0.84[JPT][hapmap]
rs877099	0.88[CHB][hapmap];0.85[JPT][hapmap]
rs918050	0.80[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv529606	chr2:40206280-40896881	Flanking Active TSS Enhancers Active TSS Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv873902	chr2:40231282-40466268	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv1000572	chr2:40271958-40458911	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv535654	chr2:40271958-40458911	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv581502	chr2:40273903-40459645	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv873904	chr2:40292289-40466268	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv873910	chr2:40391907-40466268	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	esv1851152	chr2:40393223-40512023	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
9	nsv873911	chr2:40423454-41161464	ZNF genes & repeats Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
10	nsv1008190	chr2:40429442-40506772	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
11	esv34071	chr2:40435231-40578229	Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
12	nsv524586	chr2:40447587-40497501	Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:24 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:40447800-40457600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr2:40448000-40487400	Weak transcription	Monocytes-CD14+_RO01746	blood
3	chr2:40451400-40490000	Weak transcription	Dnd41	blood
4	chr2:40453600-40457200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr2:40453600-40457200	Weak transcription	Duodenum Smooth Muscle	Duodenum
6	chr2:40453600-40459400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr2:40453800-40471000	Weak transcription	Right Ventricle	heart
8	chr2:40453800-40471400	Weak transcription	Right Atrium	heart
9	chr2:40454200-40458000	Weak transcription	Stomach Smooth Muscle	stomach
10	chr2:40454400-40458200	Weak transcription	Rectal Smooth Muscle	rectum
11	chr2:40454600-40457400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
12	chr2:40454600-40459200	Enhancers	Fetal Heart	heart
13	chr2:40455000-40456400	Enhancers	Brain Germinal Matrix	brain
14	chr2:40455400-40456000	Enhancers	Left Ventricle	heart
15	chr2:40455400-40456000	Enhancers	HSMMtube	muscle
16	chr2:40455400-40456400	Enhancers	HSMM	muscle
17	chr2:40455600-40456000	Enhancers	Fetal Brain Male	brain
18	chr2:40455600-40456000	Enhancers	Fetal Muscle Leg	muscle
19	chr2:40455600-40456000	Enhancers	Skeletal Muscle Female	skeletal muscle
20	chr2:40455600-40458000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr2:40455600-40466600	Weak transcription	Muscle Satellite Cultured Cells	--
22	chr2:40455800-40456000	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr2:40455800-40456200	Weak transcription	Aorta	Aorta
24	chr2:40455800-40457200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain

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