Variant report

Variant	rs58321514
Chromosome Location	chr3:150934988-150934989
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:150919820..150922068-chr3:150933502..150935019,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000174946	Chromatin interaction

Extended variants
information (count: 58 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:54)

rs_ID	r²[population]
rs10935846	1.00[ASN][1000 genomes]
rs12106682	1.00[EUR][1000 genomes]
rs12631155	1.00[EUR][1000 genomes]
rs16863173	1.00[EUR][1000 genomes]
rs16863219	1.00[EUR][1000 genomes]
rs16863248	1.00[EUR][1000 genomes]
rs16863250	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1873620	1.00[ASN][1000 genomes]
rs1873623	1.00[ASN][1000 genomes]
rs2870415	1.00[EUR][1000 genomes]
rs35291743	1.00[ASN][1000 genomes]
rs3821666	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs3960212	1.00[EUR][1000 genomes]
rs41526246	0.88[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs41526349	1.00[EUR][1000 genomes]
rs60356898	1.00[ASN][1000 genomes]
rs60620665	1.00[EUR][1000 genomes]
rs60816259	0.83[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60966250	1.00[EUR][1000 genomes]
rs61736003	1.00[ASN][1000 genomes]
rs6440723	1.00[EUR][1000 genomes]
rs6440725	0.89[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6767615	1.00[EUR][1000 genomes]
rs6774659	1.00[EUR][1000 genomes]
rs6776934	0.89[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6777211	0.89[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6787551	1.00[EUR][1000 genomes]
rs6790244	1.00[EUR][1000 genomes]
rs6790349	1.00[EUR][1000 genomes]
rs6794447	1.00[EUR][1000 genomes]
rs73009177	1.00[EUR][1000 genomes]
rs73012977	1.00[EUR][1000 genomes]
rs73012978	1.00[EUR][1000 genomes]
rs73012986	1.00[EUR][1000 genomes]
rs73012988	1.00[EUR][1000 genomes]
rs73012992	1.00[EUR][1000 genomes]
rs73013000	1.00[EUR][1000 genomes]
rs73014806	1.00[EUR][1000 genomes]
rs73014871	1.00[EUR][1000 genomes]
rs73014873	1.00[EUR][1000 genomes]
rs73016712	1.00[EUR][1000 genomes]
rs73016789	1.00[EUR][1000 genomes]
rs73018620	1.00[EUR][1000 genomes]
rs73019093	0.88[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73019099	0.83[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73021108	0.88[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73021116	1.00[EUR][1000 genomes]
rs73021129	1.00[EUR][1000 genomes]
rs73021144	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7618087	1.00[EUR][1000 genomes]
rs7638986	1.00[EUR][1000 genomes]
rs7653225	0.85[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs937121	1.00[ASN][1000 genomes]
rs937122	1.00[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	nsv460894	chr3:150770614-151095093	Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv592045	chr3:150770614-151095093	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
3	esv2757897	chr3:150791625-150957485	ZNF genes & repeats Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	esv2759188	chr3:150791625-150957485	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:150878000-150946000	Weak transcription	Placenta	Placenta
2	chr3:150928200-150936000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr3:150928800-150943800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr3:150928800-150946200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr3:150928800-150952800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr3:150928800-150953000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr3:150929000-150935000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr3:150929000-150938200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
9	chr3:150929000-150943200	Weak transcription	Psoas Muscle	Psoas
10	chr3:150929000-150945200	Weak transcription	Primary B cells from peripheral blood	blood
11	chr3:150929200-150935000	Weak transcription	HUES64 Cell Line	embryonic stem cell
12	chr3:150929200-150938000	Weak transcription	HUES6 Cell Line	embryonic stem cell
13	chr3:150929200-150945400	Weak transcription	HUES48 Cell Line	embryonic stem cell
14	chr3:150929600-150939200	Weak transcription	Primary hematopoietic stem cells	blood
15	chr3:150929800-150935200	Weak transcription	Liver	Liver
16	chr3:150931400-150936000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr3:150932200-150935000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr3:150932200-150936800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr3:150932200-150942800	Weak transcription	Primary neutrophils fromperipheralblood	blood
20	chr3:150932400-150937400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr3:150932400-150938200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr3:150932600-150946200	Weak transcription	H9 Cell Line	embryonic stem cell
23	chr3:150933200-150935600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr3:150933400-150937200	Strong transcription	Primary B cells from cord blood	blood
25	chr3:150933400-150937600	Enhancers	NHDF-Ad	bronchial
26	chr3:150933400-150937800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr3:150933600-150935400	Enhancers	Adipose Nuclei	Adipose
28	chr3:150933600-150937200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr3:150933600-150937400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr3:150933600-150937600	Enhancers	NH-A	brain
31	chr3:150933600-150937600	Enhancers	NHLF	lung
32	chr3:150933800-150935000	Weak transcription	Left Ventricle	heart
33	chr3:150933800-150936800	Weak transcription	Skeletal Muscle Female	skeletal muscle
34	chr3:150934000-150935400	Enhancers	Brain Anterior Caudate	brain
35	chr3:150934200-150935400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr3:150934200-150935600	Enhancers	Muscle Satellite Cultured Cells	--
37	chr3:150934200-150937400	Enhancers	Osteobl	bone
38	chr3:150934400-150935000	Enhancers	Colon Smooth Muscle	Colon
39	chr3:150934400-150935400	Enhancers	iPS-18 Cell Line	embryonic stem cell
40	chr3:150934400-150935800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr3:150934600-150935200	Enhancers	Stomach Smooth Muscle	stomach
42	chr3:150934600-150935400	Enhancers	Aorta	Aorta
43	chr3:150934600-150935400	Enhancers	Rectal Smooth Muscle	rectum
44	chr3:150934600-150935600	Enhancers	Fetal Stomach	stomach
45	chr3:150934600-150937000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
46	chr3:150934600-150937200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr3:150934600-150939000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
48	chr3:150934800-150935000	Flanking Active TSS	Fetal Heart	heart
49	chr3:150934800-150935400	Enhancers	HSMMtube	muscle
50	chr3:150934800-150936000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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