Variant report

Variant	rs1017047
Chromosome Location	chr7:71448155-71448156
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 62 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs1003685	0.82[ASN][1000 genomes]
rs10229928	0.85[CHB][hapmap]
rs10231062	1.00[CHB][hapmap];0.95[JPT][hapmap];0.86[ASN][1000 genomes]
rs10252249	0.85[ASN][1000 genomes]
rs10258507	0.86[CHB][hapmap]
rs10265141	1.00[CHB][hapmap];0.95[JPT][hapmap];0.86[ASN][1000 genomes]
rs10273495	1.00[CHB][hapmap];0.95[JPT][hapmap];0.86[ASN][1000 genomes]
rs10280279	1.00[CHB][hapmap];0.95[JPT][hapmap];0.86[ASN][1000 genomes]
rs10280568	0.83[CHB][hapmap];0.95[JPT][hapmap]
rs1034806	0.90[CHB][hapmap];0.83[JPT][hapmap];0.81[ASN][1000 genomes]
rs1099451	0.90[CHB][hapmap]
rs12666489	0.90[ASN][1000 genomes]
rs12666891	0.86[ASN][1000 genomes]
rs12671441	0.86[ASN][1000 genomes]
rs17137604	0.90[CHB][hapmap];0.83[JPT][hapmap]
rs17137608	0.90[CHB][hapmap]
rs17144164	0.90[CHB][hapmap]
rs17144232	1.00[CHB][hapmap];0.95[JPT][hapmap];0.86[ASN][1000 genomes]
rs17144240	1.00[CHB][hapmap];0.95[JPT][hapmap];0.92[ASN][1000 genomes]
rs17144279	0.89[JPT][hapmap]
rs17144283	0.87[JPT][hapmap]
rs2867564	0.90[CHB][hapmap];0.83[JPT][hapmap];0.81[ASN][1000 genomes]
rs2867565	0.81[ASN][1000 genomes]
rs35720869	0.84[ASN][1000 genomes]
rs57375990	0.97[ASN][1000 genomes]
rs58064021	0.86[ASN][1000 genomes]
rs58173010	0.97[ASN][1000 genomes]
rs58251256	0.96[ASN][1000 genomes]
rs6955049	0.83[CHB][hapmap];0.91[JPT][hapmap]
rs6965309	0.95[CHB][hapmap];0.95[JPT][hapmap];0.82[ASN][1000 genomes]
rs6980132	0.90[CHB][hapmap];0.83[JPT][hapmap];0.83[ASN][1000 genomes]
rs72506800	0.95[ASN][1000 genomes]
rs72506801	0.94[ASN][1000 genomes]
rs844684	0.85[CHB][hapmap]
rs844691	0.81[ASN][1000 genomes]
rs844692	0.90[CHB][hapmap];0.82[ASN][1000 genomes]
rs844693	0.90[CHB][hapmap];0.82[ASN][1000 genomes]
rs844694	0.90[CHB][hapmap];0.82[ASN][1000 genomes]
rs844695	0.83[ASN][1000 genomes]
rs844696	0.82[ASN][1000 genomes]
rs844698	0.81[ASN][1000 genomes]
rs844699	0.90[CHB][hapmap];0.84[ASN][1000 genomes]
rs844701	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs844702	0.82[ASN][1000 genomes]
rs844705	0.90[CHB][hapmap]
rs844712	0.84[ASN][1000 genomes]
rs844790	0.90[CHB][hapmap]
rs844791	0.95[CHB][hapmap]
rs844793	0.90[CHB][hapmap]
rs844795	0.90[CHB][hapmap]
rs844796	0.90[CHB][hapmap]
rs844797	0.84[ASN][1000 genomes]
rs917209	0.82[CHB][hapmap]

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	nsv1026896	chr7:71003462-71721516	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv1027496	chr7:71162362-71575116	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv916220	chr7:71200006-71708048	Strong transcription Flanking Active TSS ZNF genes & repeats Enhancers Weak transcription Genic enhancers Bivalent/Poised TSS Active TSS Bivalent Enhancer 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
4	nsv531372	chr7:71300090-71909517	Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
5	nsv1017367	chr7:71339782-71476575	ZNF genes & repeats Active TSS Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
6	nsv888344	chr7:71406392-71488833	ZNF genes & repeats Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
7	nsv888345	chr7:71408360-71485245	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
8	nsv491610	chr7:71422560-71803630	Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS 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	4 gene(s)	inside rSNPs	diseases
9	nsv831023	chr7:71443549-71588033	Enhancers Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:71441400-71452800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr7:71445800-71448400	Enhancers	Dnd41	blood
3	chr7:71445800-71448600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr7:71447200-71448400	Enhancers	Fetal Thymus	thymus
5	chr7:71447200-71449800	Weak transcription	Thymus	Thymus
6	chr7:71447200-71452400	Weak transcription	Primary hematopoietic stem cells	blood
7	chr7:71447800-71448600	Enhancers	Primary T cells from cord blood	blood
8	chr7:71448000-71448600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr7:71448000-71452000	Weak transcription	Primary hematopoietic stem cells short term culture	blood

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