Variant report

Variant	rs45486305
Chromosome Location	chr6:70882307-70882308
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	chr6:70877283..70879932-chr6:70881607..70883898,2	K562	blood:
2	chr6:70877239..70879932-chr6:70881607..70883677,2	K562	blood:

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs1200564	0.97[EUR][1000 genomes]
rs1200565	0.97[EUR][1000 genomes]
rs1200566	0.97[EUR][1000 genomes]
rs1200567	0.94[EUR][1000 genomes]
rs1517043	1.00[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs16868641	1.00[EUR][1000 genomes]
rs17690121	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17692231	0.89[AMR][1000 genomes]
rs17692261	0.89[AMR][1000 genomes]
rs17692395	0.89[AMR][1000 genomes]
rs17712342	0.88[EUR][1000 genomes]
rs17747228	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs476026	1.00[EUR][1000 genomes]
rs476740	1.00[EUR][1000 genomes]
rs487928	0.97[EUR][1000 genomes]
rs540654	0.97[EUR][1000 genomes]
rs558856	1.00[EUR][1000 genomes]
rs577010	1.00[EUR][1000 genomes]
rs607716	1.00[EUR][1000 genomes]
rs661521	0.97[EUR][1000 genomes]
rs737331	0.88[EUR][1000 genomes]
rs73746881	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1026151	chr6:70621616-70946967	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv933674	chr6:70663616-70973112	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv932111	chr6:70736835-71633094	Enhancers Active TSS Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
4	nsv886142	chr6:70741209-71251421	Weak transcription Strong transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
5	nsv830683	chr6:70743422-70941190	Bivalent Enhancer Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv1015807	chr6:70874416-70913489	Strong transcription Enhancers Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:70856200-70899400	Weak transcription	Left Ventricle	heart
2	chr6:70875600-70919800	Weak transcription	GM12878-XiMat	blood
3	chr6:70881000-70884200	Strong transcription	Primary B cells from peripheral blood	blood
4	chr6:70881000-70893600	Weak transcription	Fetal Heart	heart
5	chr6:70882200-70882600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr6:70882200-70884000	Strong transcription	Primary B cells from cord blood	blood

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