Variant report

Variant	rs10009686
Chromosome Location	chr4:86514731-86514732
allele	A/C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr4:86512935..86515242-chr4:86516112..86518859,2	K562	blood:
2	chr4:86513228..86515931-chr4:86524636..86526481,2	K562	blood:
3	chr4:86498940..86503292-chr4:86514616..86519116,5	K562	blood:

Variant related genes	Relation type
ENSG00000138639	Chromatin interaction

Extended variants
information (count: 46 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs10003508	1.00[AMR][1000 genomes]
rs10003616	1.00[AMR][1000 genomes]
rs10006491	1.00[AMR][1000 genomes]
rs10009042	1.00[AMR][1000 genomes]
rs10015628	1.00[AMR][1000 genomes]
rs10016029	1.00[AMR][1000 genomes]
rs10016153	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10020940	1.00[AMR][1000 genomes]
rs10023579	1.00[AMR][1000 genomes]
rs10030914	1.00[AMR][1000 genomes]
rs10031920	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10033604	1.00[AMR][1000 genomes]
rs13434500	1.00[AMR][1000 genomes]
rs13435619	1.00[AMR][1000 genomes]
rs28380594	1.00[AMR][1000 genomes]
rs28385277	1.00[AMR][1000 genomes]
rs28385531	1.00[AMR][1000 genomes]
rs28404254	1.00[AMR][1000 genomes]
rs28416247	1.00[AMR][1000 genomes]
rs28417307	1.00[AMR][1000 genomes]
rs28446374	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28463959	1.00[AMR][1000 genomes]
rs28483739	1.00[AMR][1000 genomes]
rs28493605	1.00[AMR][1000 genomes]
rs28542843	1.00[AMR][1000 genomes]
rs28556771	1.00[AMR][1000 genomes]
rs28568576	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28585433	1.00[AMR][1000 genomes]
rs28607329	1.00[AMR][1000 genomes]
rs28618270	1.00[AMR][1000 genomes]
rs28645081	1.00[AMR][1000 genomes]
rs28652904	1.00[AMR][1000 genomes]
rs28663637	1.00[AMR][1000 genomes]
rs28671522	1.00[AMR][1000 genomes]
rs28708671	1.00[AMR][1000 genomes]
rs28733613	1.00[AMR][1000 genomes]
rs72976713	1.00[AMR][1000 genomes]
rs72976727	1.00[AMR][1000 genomes]
rs9996146	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv519588	chr4:85762385-86591202	Weak transcription Enhancers Strong transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
2	nsv461566	chr4:85988032-86725502	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
3	nsv594747	chr4:85988032-86725502	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
4	nsv470048	chr4:85998783-86720838	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
5	esv3450999	chr4:86485840-86773745	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA	2 gene(s)	inside rSNPs	diseases
6	nsv829999	chr4:86500257-86666019	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Genic enhancers Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA	2 gene(s)	inside rSNPs	diseases
7	esv1803586	chr4:86503425-86516352	Genic enhancers Enhancers Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:86487200-86521200	Weak transcription	HSMMtube	muscle
2	chr4:86492600-86517000	Weak transcription	Adipose Nuclei	Adipose
3	chr4:86495000-86516200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr4:86497400-86516800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr4:86502000-86517200	Weak transcription	HSMM	muscle
6	chr4:86509600-86516000	Weak transcription	Primary B cells from peripheral blood	blood
7	chr4:86513000-86515400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr4:86513000-86516400	Weak transcription	Stomach Mucosa	stomach
9	chr4:86513000-86522600	Weak transcription	Primary B cells from cord blood	blood
10	chr4:86513200-86516200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland

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