Variant report

Variant	rs10836083
Chromosome Location	chr11:33642235-33642236
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs11032313	1.00[EUR][1000 genomes]
rs12364510	1.00[EUR][1000 genomes]
rs1474773	1.00[EUR][1000 genomes]
rs1474774	1.00[EUR][1000 genomes]
rs73492971	1.00[EUR][1000 genomes]
rs959000	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1044478	chr11:33008435-33656273	Enhancers Strong transcription Flanking Active TSS Genic enhancers Weak transcription Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	65 gene(s)	inside rSNPs	diseases
2	nsv1050944	chr11:33043155-33656273	Flanking Active TSS Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
3	nsv540993	chr11:33043155-33656273	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
4	nsv869418	chr11:33053073-33662479	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
5	nsv832112	chr11:33469782-33683052	Enhancers Strong transcription Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv832113	chr11:33609202-33767781	Transcr. at gene 5' and 3' Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 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	chr11:33594600-33644000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr11:33605800-33642400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr11:33627200-33643400	Weak transcription	HSMMtube	muscle
4	chr11:33628800-33642400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr11:33632800-33642400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr11:33633800-33652400	Weak transcription	Fetal Brain Female	brain
7	chr11:33634600-33643800	Weak transcription	HUVEC	blood vessel
8	chr11:33635000-33644800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr11:33638800-33644800	Enhancers	HMEC	breast
10	chr11:33639000-33643000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr11:33639800-33642400	Weak transcription	Brain Cingulate Gyrus	brain
12	chr11:33639800-33642600	Weak transcription	HSMM	muscle
13	chr11:33640200-33642600	Weak transcription	HUES48 Cell Line	embryonic stem cell
14	chr11:33640200-33642600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
15	chr11:33640600-33666400	Weak transcription	Brain Germinal Matrix	brain
16	chr11:33640800-33645400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr11:33640800-33673600	Weak transcription	Fetal Brain Male	brain
18	chr11:33641000-33644400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr11:33641200-33644400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr11:33641400-33642800	Enhancers	NHEK	skin
21	chr11:33641400-33643000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr11:33641400-33643000	Enhancers	Brain Angular Gyrus	brain
23	chr11:33641400-33645000	Enhancers	Breast Myoepithelial Primary Cells	Breast
24	chr11:33641600-33642800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr11:33641600-33643000	Enhancers	Brain Anterior Caudate	brain
26	chr11:33641600-33643600	Enhancers	Muscle Satellite Cultured Cells	--
27	chr11:33641600-33644200	Enhancers	NHDF-Ad	bronchial
28	chr11:33641600-33644400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr11:33641800-33642800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
30	chr11:33641800-33643000	Enhancers	Brain Hippocampus Middle	brain
31	chr11:33641800-33644600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr11:33642000-33643000	Enhancers	Adipose Nuclei	Adipose
33	chr11:33642000-33643400	Enhancers	Brain Substantia Nigra	brain
34	chr11:33642000-33644400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr11:33642000-33644400	Enhancers	NH-A	brain
36	chr11:33642000-33644600	Enhancers	Osteobl	bone
37	chr11:33642200-33642600	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
38	chr11:33642200-33642600	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
39	chr11:33642200-33642800	Enhancers	Fetal Muscle Leg	muscle

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