Variant report

Variant	rs58361598
Chromosome Location	chr11:71871788-71871789
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:71823336..71825069-chr11:71869762..71871942,2	K562	blood:
2	chr11:71855220..71857768-chr11:71870927..71873588,3	K562	blood:
3	chr11:71870250..71872525-chr11:71873469..71876026,2	K562	blood:

Variant related genes	Relation type
ENSG00000110200	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs55649541	1.00[AFR][1000 genomes]
rs55673306	0.83[AFR][1000 genomes]
rs55680751	1.00[AFR][1000 genomes]
rs55804025	1.00[AFR][1000 genomes]
rs55837642	1.00[AFR][1000 genomes]
rs55860698	1.00[AFR][1000 genomes]
rs55922008	1.00[AFR][1000 genomes]
rs56160537	0.83[AFR][1000 genomes]
rs56270043	1.00[AFR][1000 genomes]
rs56666776	1.00[AFR][1000 genomes]
rs57927868	1.00[AFR][1000 genomes]
rs58219059	1.00[AFR][1000 genomes]
rs58408933	0.83[AFR][1000 genomes]
rs58724377	1.00[AFR][1000 genomes]
rs59382154	1.00[AFR][1000 genomes]
rs59487998	1.00[AFR][1000 genomes]
rs59564576	1.00[AFR][1000 genomes]
rs59782279	0.83[AFR][1000 genomes]
rs60381558	1.00[AFR][1000 genomes]
rs60700557	1.00[AFR][1000 genomes]
rs60909653	1.00[AFR][1000 genomes]
rs61318449	1.00[AFR][1000 genomes]
rs61378805	1.00[AFR][1000 genomes]
rs61559889	1.00[AFR][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	nsv530623	chr11:71088949-72020418	Enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	134 gene(s)	inside rSNPs	diseases
2	nsv1054858	chr11:71847797-71880291	Enhancers Flanking Active TSS Genic enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	esv3493111	chr11:71850822-71893073	Weak transcription Genic enhancers Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	esv3493112	chr11:71850822-71893073	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
5	nsv435918	chr11:71851427-71890983	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
6	esv5948	chr11:71851479-71890582	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
7	esv3359634	chr11:71851533-71892403	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
8	esv2513904	chr11:71852934-71892793	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
9	nsv526086	chr11:71867167-71872777	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 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	chr11:71868400-71874000	Weak transcription	K562	blood
2	chr11:71868600-71873200	Weak transcription	NHEK	skin
3	chr11:71871200-71871800	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr11:71871400-71871800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr11:71871600-71871800	Enhancers	NHLF	lung
6	chr11:71871600-71874000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr11:71871600-71874800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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