Variant report

Variant	rs11826066
Chromosome Location	chr11:86172176-86172177
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:86169916..86172612-chr11:86280492..86283245,2	MCF-7	breast:
2	chr11:86168596..86172615-chr11:86512849..86516301,3	MCF-7	breast:
3	chr11:86170892..86174262-chr11:86177724..86181309,3	MCF-7	breast:
4	chr11:86160742..86163401-chr11:86170185..86172480,2	MCF-7	breast:
5	chr11:86171384..86173382-chr11:86174243..86177656,3	MCF-7	breast:

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs11234648	1.00[MEX][hapmap];0.88[TSI][hapmap]
rs11234667	1.00[GIH][hapmap]
rs11819827	1.00[CEU][hapmap]
rs11825033	0.82[CEU][hapmap];0.90[EUR][1000 genomes]
rs12269969	0.90[EUR][1000 genomes]
rs12278188	0.85[CEU][hapmap]
rs12280555	0.88[TSI][hapmap]
rs12281596	0.85[CEU][hapmap]
rs2078385	0.88[TSI][hapmap]
rs751911	1.00[CEU][hapmap];0.81[EUR][1000 genomes]
rs7936577	0.85[CEU][hapmap];0.84[EUR][1000 genomes]
rs7952019	1.00[CEU][hapmap];0.88[TSI][hapmap];0.81[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1044081	chr11:86133641-86868560	Bivalent/Poised TSS Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
2	nsv541118	chr11:86133641-86868560	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
3	nsv898056	chr11:86156848-86304402	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:78 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:86152400-86172200	Weak transcription	Fetal Brain Male	brain
2	chr11:86153200-86187000	Weak transcription	Fetal Kidney	kidney
3	chr11:86157000-86179800	Weak transcription	Fetal Intestine Large	intestine
4	chr11:86158600-86187200	Weak transcription	Duodenum Mucosa	Duodenum
5	chr11:86159600-86196800	Weak transcription	Primary hematopoietic stem cells	blood
6	chr11:86159800-86172600	Weak transcription	Fetal Brain Female	brain
7	chr11:86160200-86221000	Weak transcription	Primary T cells from cord blood	blood
8	chr11:86160800-86173400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr11:86167000-86172800	Enhancers	HUVEC	blood vessel
10	chr11:86167400-86172600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr11:86167400-86172800	Enhancers	Adipose Nuclei	Adipose
12	chr11:86167400-86172800	Enhancers	Right Atrium	heart
13	chr11:86167600-86172200	Enhancers	Breast Myoepithelial Primary Cells	Breast
14	chr11:86167600-86172200	Enhancers	HMEC	breast
15	chr11:86168200-86175600	Weak transcription	Rectal Mucosa Donor 31	rectum
16	chr11:86168400-86172200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr11:86169000-86172200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr11:86169400-86172200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr11:86169400-86172200	Enhancers	Osteobl	bone
20	chr11:86169400-86172800	Enhancers	Fetal Muscle Leg	muscle
21	chr11:86169400-86172800	Enhancers	HSMMtube	muscle
22	chr11:86169400-86174800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr11:86169600-86172200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr11:86169600-86172200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr11:86169600-86172200	Enhancers	Muscle Satellite Cultured Cells	--
26	chr11:86169600-86172200	Enhancers	NHDF-Ad	bronchial
27	chr11:86169600-86172600	Enhancers	HSMM	muscle
28	chr11:86169800-86172200	Enhancers	NH-A	brain
29	chr11:86169800-86172200	Enhancers	NHLF	lung
30	chr11:86169800-86172800	Enhancers	Skeletal Muscle Male	skeletal muscle
31	chr11:86169800-86176200	Enhancers	NHEK	skin
32	chr11:86169800-86178400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr11:86170000-86172800	Enhancers	Skeletal Muscle Female	skeletal muscle
34	chr11:86170200-86172400	Enhancers	Fetal Heart	heart
35	chr11:86170200-86187200	Weak transcription	Stomach Mucosa	stomach
36	chr11:86170400-86172400	Enhancers	Brain Anterior Caudate	brain
37	chr11:86170400-86172800	Enhancers	Cortex derived primary cultured neurospheres	brain
38	chr11:86170600-86172200	Enhancers	Left Ventricle	heart
39	chr11:86170600-86172400	Enhancers	Brain Cingulate Gyrus	brain
40	chr11:86170600-86172400	Enhancers	Brain Substantia Nigra	brain
41	chr11:86170600-86172600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr11:86170600-86172600	Enhancers	Brain Hippocampus Middle	brain
43	chr11:86170600-86172600	Enhancers	Right Ventricle	heart
44	chr11:86170600-86172800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr11:86170800-86172200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
46	chr11:86170800-86172200	Enhancers	HUES6 Cell Line	embryonic stem cell
47	chr11:86170800-86172200	Enhancers	Pancreas	Pancrea
48	chr11:86170800-86172400	Enhancers	Brain Angular Gyrus	brain
49	chr11:86170800-86172400	Enhancers	Brain Inferior Temporal Lobe	brain
50	chr11:86170800-86172800	Enhancers	Fetal Muscle Trunk	muscle

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