Variant report

Variant	rs6863571
Chromosome Location	chr5:17089813-17089814
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 32 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10050750	0.92[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs12109054	0.94[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs12514216	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12519524	0.94[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs12520008	0.94[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs12521131	0.94[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs13189103	0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2086607	0.88[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs2101149	0.81[ASN][1000 genomes]
rs2128311	0.93[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs2128312	0.93[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs2170526	0.88[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs28412452	0.94[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs34398449	0.91[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs34738571	0.84[AMR][1000 genomes]
rs35725865	0.94[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs4702194	0.81[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs6554967	0.84[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs6872871	0.94[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs6874789	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6889105	0.92[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs6896287	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1025225	chr5:16714512-17234866	Enhancers Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
2	nsv1015247	chr5:16748966-17133274	Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Strong transcription Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
3	nsv880277	chr5:16829442-17316288	Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
4	esv3510797	chr5:16966764-17125849	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	esv3510798	chr5:16966764-17125849	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv1017222	chr5:17001819-17133274	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	nsv1021972	chr5:17011758-17091878	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	nsv1026025	chr5:17039665-17195440	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
9	nsv1027435	chr5:17068441-17095350	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
10	nsv969212	chr5:17070735-17098476	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:17082200-17090000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr5:17085000-17090000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr5:17087600-17090000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr5:17087600-17090200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr5:17087600-17093800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr5:17089200-17090200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr5:17089200-17090200	Enhancers	NHEK	skin
8	chr5:17089400-17090400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr5:17089600-17090600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr5:17089600-17090600	Enhancers	Osteobl	bone

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