Variant report

Variant	rs7189437
Chromosome Location	chr16:80560672-80560673
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

No data

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr16:80560034..80561852-chr16:80885706..80886850,17	MCF-7	breast:
2	chr16:80560536..80561900-chr16:80858338..80859410,14	MCF-7	breast:
3	chr16:79103992..79106685-chr16:80558590..80561152,2	K562	blood:
4	chr16:80559928..80561785-chr16:80653051..80655923,2	MCF-7	breast:
5	chr16:80560059..80562846-chr16:80837762..80839641,2	MCF-7	breast:
6	chr16:80559100..80562719-chr16:80573545..80577468,3	MCF-7	breast:
7	chr16:80559326..80561966-chr16:80751074..80753973,2	MCF-7	breast:
8	chr16:80467020..80469434-chr16:80558552..80560756,2	K562	blood:
9	chr16:80560152..80563115-chr16:80649804..80651965,3	MCF-7	breast:

No data

No data

No data

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs4577099	0.84[ASN][1000 genomes]
rs7190501	0.84[ASN][1000 genomes]
rs8048886	0.85[ASN][1000 genomes]
rs8059886	0.84[ASN][1000 genomes]
rs9806915	0.85[ASN][1000 genomes]
rs9806977	0.84[ASN][1000 genomes]
rs9928594	0.84[ASN][1000 genomes]
rs9935535	0.84[ASN][1000 genomes]
rs9938023	0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv907001	chr16:80405292-80620611	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv833300	chr16:80475066-80601036	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	nsv1060621	chr16:80532848-80980616	Weak transcription Active TSS ZNF genes & repeats Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
4	nsv542989	chr16:80532848-80980616	Enhancers Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:80558800-80561000	Enhancers	Fetal Kidney	kidney
2	chr16:80560200-80560800	Enhancers	Primary T helper cells PMA-I stimulated	--
3	chr16:80560200-80561000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
4	chr16:80560400-80560800	Enhancers	Liver	Liver
5	chr16:80560600-80560800	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr16:80560600-80560800	Enhancers	Adipose Nuclei	Adipose
7	chr16:80560600-80560800	Enhancers	Fetal Intestine Small	intestine
8	chr16:80560600-80560800	Enhancers	Placenta	Placenta
9	chr16:80560600-80561000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
10	chr16:80560600-80561000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr16:80560600-80561000	Enhancers	Duodenum Mucosa	Duodenum
12	chr16:80560600-80561400	Enhancers	Primary T cells fromperipheralblood	blood

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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