Variant report

Variant	rs34682370
Chromosome Location	chr2:40667872-40667873
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	chr2:40662045..40663958-chr2:40665740..40668580,2	MCF-7	breast:

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs12999886	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs13031545	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13031785	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13031843	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13031849	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13035085	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17025999	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17026001	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17026003	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17026005	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17026009	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17026011	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17026012	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17026014	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17026018	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs34038561	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs35321042	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs35478019	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35797248	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs35923316	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4993292	0.98[ASN][1000 genomes]
rs57193459	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs61629255	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs71439297	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs71439298	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs71439299	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv529606	chr2:40206280-40896881	Flanking Active TSS Enhancers Active TSS Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv873911	chr2:40423454-41161464	ZNF genes & repeats Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	esv2757794	chr2:40547947-40733776	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	esv2759044	chr2:40547947-40733776	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv2700	chr2:40667461-40712805	Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:39 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:40646600-40670800	Weak transcription	Fetal Brain Female	brain
2	chr2:40648200-40676400	Weak transcription	Fetal Kidney	kidney
3	chr2:40653000-40674800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr2:40657000-40671200	Weak transcription	Fetal Stomach	stomach
5	chr2:40662600-40677200	Weak transcription	Fetal Muscle Leg	muscle
6	chr2:40663400-40672000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr2:40663600-40677000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr2:40663600-40677000	Weak transcription	Aorta	Aorta
9	chr2:40663800-40677600	Weak transcription	HSMMtube	muscle
10	chr2:40664600-40673000	Weak transcription	Left Ventricle	heart
11	chr2:40665000-40668200	Enhancers	Osteobl	bone
12	chr2:40665200-40668400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr2:40665200-40668600	Enhancers	Muscle Satellite Cultured Cells	--
14	chr2:40665200-40675200	Weak transcription	Stomach Smooth Muscle	stomach
15	chr2:40665400-40674800	Weak transcription	NHLF	lung
16	chr2:40665800-40668000	Weak transcription	Dnd41	blood
17	chr2:40666600-40673400	Weak transcription	Colon Smooth Muscle	Colon
18	chr2:40666600-40676400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr2:40666600-40676600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr2:40666600-40677200	Weak transcription	Right Ventricle	heart
21	chr2:40666800-40671200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr2:40666800-40675400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr2:40667000-40670000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr2:40667000-40672400	Weak transcription	Brain Anterior Caudate	brain
25	chr2:40667000-40676200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
26	chr2:40667000-40676400	Weak transcription	HMEC	breast
27	chr2:40667200-40675200	Weak transcription	NHDF-Ad	bronchial
28	chr2:40667400-40669800	Enhancers	Fetal Heart	heart
29	chr2:40667600-40668000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
30	chr2:40667600-40669000	Enhancers	Primary monocytes fromperipheralblood	blood
31	chr2:40667800-40668000	Enhancers	Duodenum Smooth Muscle	Duodenum
32	chr2:40667800-40668200	Enhancers	Liver	Liver
33	chr2:40667800-40668400	Enhancers	Primary B cells from cord blood	blood
34	chr2:40667800-40668400	Enhancers	Primary hematopoietic stem cells	blood
35	chr2:40667800-40668400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr2:40667800-40668600	Enhancers	Primary hematopoietic stem cells short term culture	blood
37	chr2:40667800-40668800	Enhancers	Primary neutrophils fromperipheralblood	blood
38	chr2:40667800-40668800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr2:40667800-40670400	Weak transcription	HSMM	muscle

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