Variant report

Variant	rs7001425
Chromosome Location	chr8:91175107-91175108
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr8:91160123..91162835-chr8:91174934..91176685,2	K562	blood:
2	chr8:91152815..91155655-chr8:91173130..91176716,3	K562	blood:
3	chr8:91152980..91155385-chr8:91174154..91176618,2	K562	blood:

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs10504888	0.91[JPT][hapmap]
rs10504891	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12675530	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs16902273	0.91[JPT][hapmap]
rs16902355	0.91[JPT][hapmap]
rs16902558	0.91[JPT][hapmap]
rs16903927	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs16904011	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs16904016	0.84[ASN][1000 genomes]
rs16904073	1.00[CEU][hapmap]
rs1805824	0.81[JPT][hapmap]
rs1805826	0.81[JPT][hapmap]
rs1805837	0.81[JPT][hapmap]
rs1805855	0.91[JPT][hapmap]
rs1805862	0.91[JPT][hapmap]
rs1805880	0.91[JPT][hapmap]
rs1805882	0.91[JPT][hapmap]
rs1805885	0.91[JPT][hapmap]
rs1805888	0.91[JPT][hapmap]
rs1805894	1.00[CEU][hapmap];0.84[CHB][hapmap];0.91[JPT][hapmap]
rs1805901	1.00[CEU][hapmap];0.84[CHB][hapmap];0.91[JPT][hapmap]
rs1805902	1.00[CEU][hapmap];0.84[CHB][hapmap];0.82[JPT][hapmap]
rs1805907	1.00[CEU][hapmap];0.84[CHB][hapmap];0.83[JPT][hapmap]
rs1805911	1.00[CEU][hapmap];0.84[CHB][hapmap];0.91[JPT][hapmap]
rs1805912	1.00[CEU][hapmap];0.91[JPT][hapmap]
rs1805914	1.00[CEU][hapmap];0.84[CHB][hapmap];0.91[JPT][hapmap]
rs1805915	1.00[CEU][hapmap];0.84[CHB][hapmap];0.91[JPT][hapmap]
rs2074594	0.91[JPT][hapmap]
rs2074595	0.91[JPT][hapmap]
rs3026287	1.00[CEU][hapmap];0.84[CHB][hapmap];0.91[JPT][hapmap]
rs35822955	0.84[AFR][1000 genomes]
rs3758145	1.00[CHB][hapmap];0.91[JPT][hapmap];0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4987078	0.84[AFR][1000 genomes]
rs6982611	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6997558	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs769418	0.81[JPT][hapmap]
rs7813378	0.91[JPT][hapmap]
rs7818433	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7822786	0.91[JPT][hapmap]
rs7826471	0.91[JPT][hapmap]
rs7836381	0.96[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7844005	0.91[JPT][hapmap]
rs7845155	0.91[JPT][hapmap]
rs7845669	0.91[JPT][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	esv2758164	chr8:91000786-91329669	Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	esv2759628	chr8:91000786-91329669	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
3	esv2757281	chr8:91090821-91235335	Weak transcription Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
4	esv34347	chr8:91101339-91179126	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
5	nsv470225	chr8:91113616-91229254	Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
6	nsv891184	chr8:91114698-91222654	Active TSS Genic enhancers Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
7	nsv824687	chr8:91144854-91177488	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
8	esv35109	chr8:91150726-91226940	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	8 gene(s)	inside rSNPs	diseases
9	nsv818643	chr8:91153308-91212148	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers	Chromatin interactive region	8 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	chr8:91163200-91176600	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr8:91173000-91176400	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr8:91173600-91176400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr8:91174000-91176400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
5	chr8:91174200-91176400	Weak transcription	Cortex derived primary cultured neurospheres	brain
6	chr8:91174400-91175800	Weak transcription	K562	blood
7	chr8:91174400-91176600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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