Variant report

No.	Distal block	Cell Line	Cell type
1	chr8:96014207..96016501-chr8:96023087..96024953,2	MCF-7	breast:
2	chr8:96010656..96013460-chr8:96013847..96015745,3	K562	blood:
3	chr8:95952618..95955139-chr8:96012632..96015406,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000164938	Chromatin interaction

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs1320165	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2459968	1.00[AMR][1000 genomes]
rs2599717	1.00[YRI][hapmap]
rs2678830	1.00[YRI][hapmap]
rs297553	1.00[YRI][hapmap]
rs297558	1.00[YRI][hapmap]
rs297560	1.00[YRI][hapmap]
rs3110161	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs471691	1.00[YRI][hapmap]
rs538963	1.00[YRI][hapmap]

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	nsv1017301	chr8:95273503-96248352	Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
2	nsv539680	chr8:95273503-96248352	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
3	nsv508520	chr8:95939373-96140068	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
4	nsv524876	chr8:96000919-96027306	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:95977400-96024200	Weak transcription	Aorta	Aorta
2	chr8:95987000-96019600	Weak transcription	Lung	lung
3	chr8:95987200-96018800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr8:95997400-96018000	Weak transcription	HSMMtube	muscle
5	chr8:96001200-96023400	Weak transcription	Liver	Liver
6	chr8:96003200-96032600	Weak transcription	Gastric	stomach
7	chr8:96009000-96036400	Weak transcription	Spleen	Spleen
8	chr8:96009600-96016200	Weak transcription	Pancreas	Pancrea
9	chr8:96009800-96023000	Weak transcription	Adipose Nuclei	Adipose
10	chr8:96010400-96015400	Weak transcription	Fetal Heart	heart
11	chr8:96011200-96016000	Weak transcription	Brain Germinal Matrix	brain
12	chr8:96012000-96016000	Enhancers	Primary B cells from cord blood	blood
13	chr8:96012200-96018800	Enhancers	Primary monocytes fromperipheralblood	blood
14	chr8:96013400-96015600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr8:96013600-96014600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr8:96013600-96016000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr8:96013600-96016200	Enhancers	Primary hematopoietic stem cells	blood
18	chr8:96013600-96016400	Enhancers	Primary hematopoietic stem cells short term culture	blood
19	chr8:96013800-96015000	Enhancers	Primary neutrophils fromperipheralblood	blood
20	chr8:96014200-96014800	Enhancers	Monocytes-CD14+_RO01746	blood
21	chr8:96014200-96015800	Weak transcription	K562	blood

Quick Search: