Variant report

Variant	rs11623609
Chromosome Location	chr14:106083044-106083045
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:106081494..106086015-chr14:106227927..106231140,4	MCF-7	breast:
2	chr14:106082136..106084046-chr14:106227930..106229438,2	MCF-7	breast:

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs10130064	1.00[EUR][1000 genomes]
rs10140012	1.00[EUR][1000 genomes]
rs10147883	1.00[EUR][1000 genomes]
rs11552998	1.00[EUR][1000 genomes]
rs11845835	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11848125	1.00[EUR][1000 genomes]
rs11850206	0.90[AFR][1000 genomes]
rs11851505	1.00[EUR][1000 genomes]
rs12431652	1.00[EUR][1000 genomes]
rs12431653	1.00[EUR][1000 genomes]
rs13000	1.00[EUR][1000 genomes]
rs2104053	1.00[EUR][1000 genomes]
rs2753508	1.00[EUR][1000 genomes]
rs2753557	1.00[EUR][1000 genomes]
rs28379859	1.00[EUR][1000 genomes]
rs28539800	0.82[AFR][1000 genomes]
rs28578923	1.00[EUR][1000 genomes]
rs28581525	1.00[EUR][1000 genomes]
rs28582906	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28627103	1.00[EUR][1000 genomes]
rs28719009	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs3923867	1.00[EUR][1000 genomes]
rs4983362	1.00[EUR][1000 genomes]
rs4983477	1.00[EUR][1000 genomes]
rs4983481	1.00[EUR][1000 genomes]
rs58503622	1.00[EUR][1000 genomes]
rs60701849	1.00[EUR][1000 genomes]
rs61985562	0.95[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs61986371	1.00[EUR][1000 genomes]
rs6576114	1.00[EUR][1000 genomes]
rs6576116	0.86[AFR][1000 genomes]
rs6576119	1.00[EUR][1000 genomes]
rs6576121	1.00[EUR][1000 genomes]
rs7143643	1.00[EUR][1000 genomes]
rs7151762	1.00[EUR][1000 genomes]
rs7152374	0.90[AFR][1000 genomes]
rs7152602	0.96[AFR][1000 genomes]
rs7152890	0.95[AFR][1000 genomes]
rs7494106	1.00[EUR][1000 genomes]
rs9671515	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9671964	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9672055	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9672072	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];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	nsv530813	chr14:105607701-106453697	Strong transcription Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	149 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:106080800-106083600	Weak transcription	Primary B cells from peripheral blood	blood
2	chr14:106082400-106084200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr14:106082600-106084200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr14:106082600-106084200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr14:106082600-106084200	ZNF genes & repeats	Pancreas	Pancrea
6	chr14:106082600-106084200	ZNF genes & repeats	Spleen	Spleen
7	chr14:106082800-106083200	Weak transcription	Gastric	stomach
8	chr14:106082800-106083400	Weak transcription	Esophagus	oesophagus
9	chr14:106082800-106083800	Bivalent Enhancer	Placenta	Placenta
10	chr14:106083000-106083800	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr14:106083000-106084000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived

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