Variant report

Variant	rs7011930
Chromosome Location	chr8:91176950-91176951
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:91176914..91178549-chr8:91234676..91237074,2	K562	blood:
2	chr8:91175219..91178633-chr8:91184019..91187268,3	K562	blood:

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10104321	0.85[JPT][hapmap]
rs10106310	0.91[AFR][1000 genomes];0.81[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs10956500	0.82[EUR][1000 genomes]
rs11782032	0.85[JPT][hapmap]
rs12549107	0.85[JPT][hapmap]
rs1800645	0.85[JPT][hapmap]
rs2023555	0.84[EUR][1000 genomes]
rs2023848	0.84[CEU][hapmap];0.85[EUR][1000 genomes]
rs4961177	0.85[EUR][1000 genomes]
rs6470671	0.85[JPT][hapmap]
rs6470713	0.85[JPT][hapmap]
rs6988013	0.80[JPT][hapmap]
rs6994202	0.85[JPT][hapmap]
rs7001759	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7459577	0.85[JPT][hapmap]
rs7461859	0.84[JPT][hapmap]
rs7815279	0.85[JPT][hapmap]
rs7816237	0.84[CEU][hapmap];0.83[EUR][1000 genomes]
rs7817302	0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs988851	0.84[CEU][hapmap];0.86[TSI][hapmap];0.85[EUR][1000 genomes]

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:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:91175800-91177400	Enhancers	K562	blood
2	chr8:91175800-91178800	Enhancers	Fetal Intestine Large	intestine
3	chr8:91176200-91177800	Enhancers	HepG2	liver
4	chr8:91176400-91177000	Enhancers	H9 Cell Line	embryonic stem cell
5	chr8:91176400-91177000	Enhancers	Cortex derived primary cultured neurospheres	brain
6	chr8:91176400-91177400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr8:91176400-91177400	Enhancers	A549	lung
8	chr8:91176400-91178000	Enhancers	Fetal Heart	heart
9	chr8:91176400-91178600	Enhancers	Fetal Intestine Small	intestine
10	chr8:91176600-91177000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr8:91176800-91178200	Enhancers	Left Ventricle	heart
12	chr8:91176800-91180600	Enhancers	Ovary	ovary

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