Variant report

Variant	rs2351959
Chromosome Location	chr11:16248204-16248205
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs11023876	0.83[CEU][hapmap]
rs11023888	0.83[CEU][hapmap]
rs11023905	0.82[MEX][hapmap]
rs11023911	0.83[CEU][hapmap]
rs1393923	0.82[MEX][hapmap]
rs17539593	0.83[CEU][hapmap]
rs2351960	0.83[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv529731	chr11:16122782-16468170	Enhancers Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv897012	chr11:16189326-16283644	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv553563	chr11:16206658-16259405	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv897013	chr11:16206658-16307700	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv897014	chr11:16211343-16283644	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv467710	chr11:16219341-16266740	Active TSS Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv553564	chr11:16219341-16266740	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	nsv553565	chr11:16220289-16307700	Enhancers ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
9	nsv897015	chr11:16235962-16307700	Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:16238600-16260800	Weak transcription	Psoas Muscle	Psoas
2	chr11:16246600-16258600	Weak transcription	Fetal Intestine Large	intestine
3	chr11:16247000-16248400	Enhancers	Duodenum Mucosa	Duodenum
4	chr11:16247000-16248400	Enhancers	Fetal Heart	heart
5	chr11:16247200-16248400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr11:16247200-16248600	Enhancers	Cortex derived primary cultured neurospheres	brain
7	chr11:16247200-16248600	Enhancers	A549	lung
8	chr11:16247400-16248400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr11:16247400-16248400	Enhancers	HUVEC	blood vessel
10	chr11:16247800-16248400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr11:16247800-16248600	Enhancers	Pancreatic Islets	Pancreatic Islet
12	chr11:16248000-16248400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr11:16248000-16248400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
14	chr11:16248000-16248400	Enhancers	Rectal Mucosa Donor 29	rectum
15	chr11:16248000-16248400	Enhancers	Skeletal Muscle Female	skeletal muscle
16	chr11:16248000-16248600	Enhancers	Fetal Intestine Small	intestine
17	chr11:16248000-16249200	Enhancers	Stomach Mucosa	stomach
18	chr11:16248200-16248400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr11:16248200-16260600	Weak transcription	Fetal Lung	lung
20	chr11:16248200-16274200	Weak transcription	Pancreas	Pancrea

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