Variant report

Variant	rs11681856
Chromosome Location	chr2:40670175-40670176
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:40663877..40665800-chr2:40669222..40671159,2	MCF-7	breast:

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs11683359	0.97[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs11684372	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs17466980	0.83[EUR][1000 genomes]
rs55929619	0.94[AMR][1000 genomes]
rs6705173	0.81[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:36 , 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	chr2:40665200-40675200	Weak transcription	Stomach Smooth Muscle	stomach
12	chr2:40665400-40674800	Weak transcription	NHLF	lung
13	chr2:40666600-40673400	Weak transcription	Colon Smooth Muscle	Colon
14	chr2:40666600-40676400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr2:40666600-40676600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr2:40666600-40677200	Weak transcription	Right Ventricle	heart
17	chr2:40666800-40671200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr2:40666800-40675400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr2:40667000-40672400	Weak transcription	Brain Anterior Caudate	brain
20	chr2:40667000-40676200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
21	chr2:40667000-40676400	Weak transcription	HMEC	breast
22	chr2:40667200-40675200	Weak transcription	NHDF-Ad	bronchial
23	chr2:40667800-40670400	Weak transcription	HSMM	muscle
24	chr2:40668000-40672400	Weak transcription	Duodenum Smooth Muscle	Duodenum
25	chr2:40668200-40675600	Weak transcription	Osteobl	bone
26	chr2:40668400-40676600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr2:40668600-40671600	Weak transcription	Muscle Satellite Cultured Cells	--
28	chr2:40668600-40677200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
29	chr2:40668800-40670800	Weak transcription	Dnd41	blood
30	chr2:40668800-40670800	Weak transcription	Monocytes-CD14+_RO01746	blood
31	chr2:40668800-40673000	Weak transcription	Primary neutrophils fromperipheralblood	blood
32	chr2:40668800-40673400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr2:40669000-40670600	Weak transcription	Primary monocytes fromperipheralblood	blood
34	chr2:40669600-40676800	Weak transcription	Duodenum Mucosa	Duodenum
35	chr2:40669800-40674000	Genic enhancers	Fetal Heart	heart
36	chr2:40670000-40673800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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