Variant report

Variant	rs2893235
Chromosome Location	chr7:26034676-26034677
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:26034062..26036742-chr7:26049058..26051711,2	K562	blood:

Extended variants
information (count: 33 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10247102	0.93[ASN][1000 genomes]
rs10249225	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10252380	0.88[EUR][1000 genomes]
rs10267565	0.96[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12535387	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2076881	0.83[CEU][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2391175	1.00[CHB][hapmap];1.00[YRI][hapmap]
rs2391213	0.93[AFR][1000 genomes];0.93[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs28360688	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4515452	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4640955	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4719843	0.88[EUR][1000 genomes]
rs4719844	0.88[EUR][1000 genomes]
rs4722545	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4722548	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4722551	1.00[CHB][hapmap];1.00[YRI][hapmap]
rs4722552	0.86[AFR][1000 genomes];0.94[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4722561	0.88[EUR][1000 genomes]
rs6946189	0.86[AFR][1000 genomes];0.94[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6963094	1.00[CHB][hapmap]
rs6968046	0.86[EUR][1000 genomes]
rs6977848	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs73089457	0.83[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs766839	0.89[EUR][1000 genomes]
rs9638829	0.89[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1016813	chr7:25405859-26150509	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	108 gene(s)	inside rSNPs	diseases
2	nsv538803	chr7:25405859-26150509	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	108 gene(s)	inside rSNPs	diseases
3	nsv606432	chr7:25988185-26223294	Enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	102 gene(s)	inside rSNPs	diseases
4	nsv887848	chr7:26000137-26059739	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv606433	chr7:26007582-26050920	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
6	nsv470188	chr7:26013958-26075094	Enhancers ZNF genes & repeats Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	nsv464412	chr7:26013959-26073411	Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	nsv606434	chr7:26013959-26073411	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Active TSS	Chromatin interactive region lncRNA	3 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	chr7:26034400-26035000	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
2	chr7:26034400-26035000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
3	chr7:26034400-26035200	Enhancers	Pancreas	Pancrea
4	chr7:26034400-26036400	Enhancers	HepG2	liver
5	chr7:26034400-26036800	Enhancers	Fetal Intestine Small	intestine
6	chr7:26034400-26037000	Enhancers	Stomach Mucosa	stomach
7	chr7:26034600-26034800	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr7:26034600-26035000	Enhancers	Gastric	stomach
9	chr7:26034600-26037200	Enhancers	Fetal Intestine Large	intestine

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