Variant report

Variant	rs16868809
Chromosome Location	chr5:89884802-89884803
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr5:89881685..89883243-chr5:89883707..89886332,2	K562	blood:
2	chr5:89702901..89704875-chr5:89883811..89886789,2	K562	blood:
3	chr5:89852793..89854346-chr5:89883740..89885331,2	MCF-7	breast:
4	chr5:89883022..89885296-chr5:89901095..89903175,2	K562	blood:

Variant related genes	Relation type
ENSG00000153140	Chromatin interaction

Extended variants
information (count: 27 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10514330	0.86[AFR][1000 genomes]
rs11738461	0.86[AFR][1000 genomes]
rs11745908	0.86[AFR][1000 genomes]
rs11749693	0.86[AFR][1000 genomes]
rs13159048	0.86[AFR][1000 genomes]
rs13167847	0.86[AFR][1000 genomes]
rs13190272	0.86[AFR][1000 genomes]
rs16868841	0.86[AFR][1000 genomes]
rs16868935	0.86[AFR][1000 genomes]
rs17541517	0.86[AFR][1000 genomes]
rs17541704	0.86[AFR][1000 genomes]
rs17541912	0.86[AFR][1000 genomes]
rs17542086	0.86[AFR][1000 genomes]
rs17542921	0.86[AFR][1000 genomes]
rs17614588	0.86[AFR][1000 genomes]
rs28399862	0.86[AFR][1000 genomes]
rs34301936	0.86[AFR][1000 genomes]
rs34719862	0.86[AFR][1000 genomes]
rs66683260	0.86[AFR][1000 genomes]
rs71637308	0.86[AFR][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	nsv1021142	chr5:89102893-89897826	Active TSS Weak transcription Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
2	nsv537804	chr5:89102893-89897826	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
3	nsv432750	chr5:89410113-90137144	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
4	nsv432751	chr5:89457044-90090444	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
5	nsv529544	chr5:89523963-90412409	Weak transcription Enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
6	nsv882366	chr5:89826726-89894564	Bivalent/Poised TSS Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
7	nsv933668	chr5:89854253-89999672	Strong transcription Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:89867400-89889200	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr5:89882000-89887600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr5:89882600-89886000	Weak transcription	Placenta	Placenta
4	chr5:89882600-89887400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
5	chr5:89882800-89888800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr5:89883000-89887400	Weak transcription	HUES48 Cell Line	embryonic stem cell
7	chr5:89884600-89890400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr5:89884800-89885800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr5:89884800-89886400	Enhancers	K562	blood

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