Variant report

Variant	rs4679786
Chromosome Location	chr3:150435684-150435685
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:150320682..150323367-chr3:150434983..150438728,4	MCF-7	breast:
2	chr3:150433681..150449199-chr3:150473254..150487048,35	MCF-7	breast:

Variant related genes	Relation type
ENSG00000120742	Chromatin interaction
ENSG00000181788	Chromatin interaction
ENSG00000198843	Chromatin interaction
ENSG00000244265	Chromatin interaction

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs11713173	0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12630268	0.98[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1897488	0.93[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1897490	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1897492	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1897493	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2116688	0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2116689	0.98[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2869474	0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2869475	0.82[AFR][1000 genomes]
rs2904115	0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4234312	0.95[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4679799	0.97[EUR][1000 genomes]
rs4680240	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6795266	0.86[CHB][hapmap];0.83[CHD][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs7427065	0.98[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7631055	0.93[CEU][hapmap];1.00[JPT][hapmap];0.88[EUR][1000 genomes]
rs7652598	1.00[CEU][hapmap];0.85[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9682304	0.93[AFR][1000 genomes];0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9823709	0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9832682	0.93[CEU][hapmap];1.00[JPT][hapmap];0.93[TSI][hapmap];0.88[EUR][1000 genomes]
rs9841228	0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9859732	0.86[CHB][hapmap];0.83[CHD][hapmap];1.00[JPT][hapmap];0.81[TSI][hapmap];0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9876907	0.92[AFR][1000 genomes];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.85[ASN][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	nsv532662	chr3:150180747-150633414	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	101 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:25 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:150422200-150439400	Weak transcription	Ovary	ovary
2	chr3:150422200-150443200	Weak transcription	Lung	lung
3	chr3:150422400-150443000	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr3:150422600-150439200	Weak transcription	Primary B cells from peripheral blood	blood
5	chr3:150422600-150439200	Weak transcription	Fetal Intestine Small	intestine
6	chr3:150422600-150439400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr3:150422600-150439400	Weak transcription	Adipose Nuclei	Adipose
8	chr3:150422600-150441800	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr3:150423200-150451600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
10	chr3:150423600-150439400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
11	chr3:150423800-150439400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
12	chr3:150428400-150439600	Weak transcription	Left Ventricle	heart
13	chr3:150428600-150439200	Weak transcription	Fetal Kidney	kidney
14	chr3:150428800-150439000	Weak transcription	Brain Anterior Caudate	brain
15	chr3:150428800-150439200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr3:150429000-150439400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr3:150429200-150439400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr3:150429200-150439400	Weak transcription	Primary T cells fromperipheralblood	blood
19	chr3:150429200-150439400	Weak transcription	Primary hematopoietic stem cells	blood
20	chr3:150429200-150444600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
21	chr3:150429200-150457600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
22	chr3:150430000-150455000	Weak transcription	Primary T cells from cord blood	blood
23	chr3:150430200-150439400	Weak transcription	Fetal Thymus	thymus
24	chr3:150430400-150441600	Weak transcription	Thymus	Thymus
25	chr3:150430800-150454000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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