Variant report

Variant	rs8114866
Chromosome Location	chr20:52715640-52715641
allele	A/C
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:14)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

No data

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr20:52709593..52716717-chr20:52810616..52817994,186	MCF-7	breast:
2	chr17:59476097..59478006-chr20:52714610..52716601,2	MCF-7	breast:
3	chr17:57861820..57864479-chr20:52713391..52716346,2	MCF-7	breast:
4	chr17:56706304..56710637-chr20:52708902..52722942,22	MCF-7	breast:
5	chr20:46410730..46421216-chr20:52711028..52724253,28	MCF-7	breast:
6	chr20:52210459..52212197-chr20:52714277..52716072,2	MCF-7	breast:
7	chr20:52714890..52716728-chr9:110512982..110515116,2	MCF-7	breast:
8	chr20:52711537..52718198-chr20:52810789..52818597,362	MCF-7	breast:
9	chr17:57919102..57921149-chr20:52714565..52717562,3	MCF-7	breast:
10	chr17:56735171..56737953-chr20:52710895..52716530,6	MCF-7	breast:
11	chr17:57915689..57917658-chr20:52715520..52717034,2	MCF-7	breast:
12	chr20:52714952..52716955-chr22:39922011..39924264,2	MCF-7	breast:
13	chr17:56734263..56738304-chr20:52709856..52719047,15	MCF-7	breast:
14	chr17:56703018..56712407-chr20:52697460..52725685,93	MCF-7	breast:

No data

No data

No data

Variant related genes	Relation type
ENSG00000212195	Chromatin interaction
ENSG00000121068	Chromatin interaction
ENSG00000267280	Chromatin interaction
ENSG00000202077	Chromatin interaction
ENSG00000267131	Chromatin interaction
ENSG00000267637	Chromatin interaction
ENSG00000196562	Chromatin interaction

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs55972874	1.00[EUR][1000 genomes]
rs57886257	1.00[EUR][1000 genomes]
rs59046998	1.00[EUR][1000 genomes]
rs6022993	1.00[EUR][1000 genomes]
rs6022994	1.00[EUR][1000 genomes]
rs73914434	1.00[EUR][1000 genomes]
rs8114189	1.00[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv586224	chr20:52474850-53279490	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	338 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:52713200-52716800	Enhancers	HepG2	liver
2	chr20:52713800-52716600	Enhancers	A549	lung
3	chr20:52714000-52718000	Weak transcription	Placenta	Placenta
4	chr20:52714000-52721200	Weak transcription	HMEC	breast
5	chr20:52714000-52721800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr20:52714400-52715800	Enhancers	Primary neutrophils fromperipheralblood	blood

Quick Search:

Input of quick search could be:

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

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