Variant report

Variant	rs34063054
Chromosome Location	chr11:9717083-9717084
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 59 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:56)

rs_ID	r²[population]
rs10770056	0.89[EUR][1000 genomes]
rs10770057	0.82[EUR][1000 genomes]
rs10840283	1.00[ASN][1000 genomes]
rs10840284	1.00[ASN][1000 genomes]
rs10840286	1.00[ASN][1000 genomes]
rs10840287	1.00[ASN][1000 genomes]
rs11042457	1.00[ASN][1000 genomes]
rs11042462	1.00[ASN][1000 genomes]
rs11042464	1.00[ASN][1000 genomes]
rs11042466	1.00[ASN][1000 genomes]
rs11042467	1.00[ASN][1000 genomes]
rs11042486	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11600183	1.00[ASN][1000 genomes]
rs11601008	1.00[ASN][1000 genomes]
rs11603527	1.00[ASN][1000 genomes]
rs11607321	1.00[ASN][1000 genomes]
rs11607900	1.00[ASN][1000 genomes]
rs12291809	0.83[EUR][1000 genomes]
rs12362879	1.00[ASN][1000 genomes]
rs12364089	1.00[ASN][1000 genomes]
rs12421878	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12786236	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12789209	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12789429	1.00[ASN][1000 genomes]
rs12794270	1.00[ASN][1000 genomes]
rs12797744	1.00[ASN][1000 genomes]
rs12801958	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12803440	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12805683	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12807017	1.00[ASN][1000 genomes]
rs2010535	0.83[EUR][1000 genomes]
rs2117698	0.90[EUR][1000 genomes]
rs2117699	0.86[EUR][1000 genomes]
rs2164311	0.91[EUR][1000 genomes]
rs35806232	1.00[ASN][1000 genomes]
rs360047	0.94[EUR][1000 genomes]
rs360049	0.84[EUR][1000 genomes]
rs36089180	1.00[ASN][1000 genomes]
rs4910060	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4910486	1.00[ASN][1000 genomes]
rs4910487	1.00[ASN][1000 genomes]
rs4910488	1.00[ASN][1000 genomes]
rs4910492	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4910493	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4910497	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4993191	0.95[EUR][1000 genomes]
rs56043731	1.00[ASN][1000 genomes]
rs61878110	0.81[EUR][1000 genomes]
rs67867011	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7116226	0.84[EUR][1000 genomes]
rs72852112	1.00[ASN][1000 genomes]
rs892851	0.95[EUR][1000 genomes]
rs892852	0.95[EUR][1000 genomes]
rs892853	0.83[EUR][1000 genomes]
rs892855	0.83[EUR][1000 genomes]
rs892856	0.95[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	nsv933855	chr11:9645441-10130519	Strong transcription Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
2	nsv1053369	chr11:9647837-9876054	Genic enhancers Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Weak transcription Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
3	nsv553468	chr11:9667828-9827871	Weak transcription Genic enhancers Active TSS Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:103 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:9704200-9723600	Weak transcription	HepG2	liver
2	chr11:9710200-9758400	Weak transcription	Psoas Muscle	Psoas
3	chr11:9710400-9732800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr11:9710600-9722000	Weak transcription	Fetal Brain Female	brain
5	chr11:9711200-9732800	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr11:9711400-9718800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr11:9711400-9754400	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr11:9711600-9723600	Weak transcription	Fetal Lung	lung
9	chr11:9711600-9724000	Weak transcription	Rectal Mucosa Donor 29	rectum
10	chr11:9711600-9724400	Weak transcription	Skeletal Muscle Male	skeletal muscle
11	chr11:9711600-9725800	Weak transcription	HSMMtube	muscle
12	chr11:9711600-9729600	Weak transcription	Fetal Heart	heart
13	chr11:9711600-9730200	Weak transcription	Right Ventricle	heart
14	chr11:9711600-9731400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr11:9711600-9732800	Weak transcription	Skeletal Muscle Female	skeletal muscle
16	chr11:9711600-9733200	Weak transcription	Aorta	Aorta
17	chr11:9711600-9736600	Weak transcription	Gastric	stomach
18	chr11:9711800-9717400	Weak transcription	HSMM	muscle
19	chr11:9711800-9722000	Weak transcription	Stomach Smooth Muscle	stomach
20	chr11:9713400-9724000	Weak transcription	Small Intestine	intestine
21	chr11:9713600-9717200	Weak transcription	A549	lung
22	chr11:9713600-9723800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr11:9713600-9730000	Weak transcription	NH-A	brain
24	chr11:9714200-9717400	Weak transcription	Muscle Satellite Cultured Cells	--
25	chr11:9715000-9718800	Strong transcription	HUVEC	blood vessel
26	chr11:9715000-9718800	Strong transcription	NHDF-Ad	bronchial
27	chr11:9715000-9721600	Weak transcription	Duodenum Mucosa	Duodenum
28	chr11:9715000-9721800	Weak transcription	Fetal Kidney	kidney
29	chr11:9715200-9717800	Genic enhancers	Primary B cells from peripheral blood	blood
30	chr11:9715200-9720000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr11:9715400-9717600	Strong transcription	Left Ventricle	heart
32	chr11:9715400-9717800	Strong transcription	Lung	lung
33	chr11:9715400-9718000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr11:9715400-9718200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr11:9715400-9720000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
36	chr11:9715400-9730200	Weak transcription	Pancreas	Pancrea
37	chr11:9715600-9717600	Strong transcription	Adipose Nuclei	Adipose
38	chr11:9715600-9717600	Strong transcription	Fetal Muscle Trunk	muscle
39	chr11:9715600-9717600	Strong transcription	Sigmoid Colon	Sigmoid Colon
40	chr11:9715600-9717600	Strong transcription	NHLF	lung
41	chr11:9715600-9717800	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
42	chr11:9715600-9717800	Strong transcription	Colon Smooth Muscle	Colon
43	chr11:9715600-9717800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
44	chr11:9715600-9717800	Strong transcription	Fetal Muscle Leg	muscle
45	chr11:9715600-9717800	Strong transcription	Placenta	Placenta
46	chr11:9715600-9718200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr11:9715600-9718200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr11:9715600-9718200	Strong transcription	Primary monocytes fromperipheralblood	blood
49	chr11:9715600-9718200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr11:9715600-9719400	Strong transcription	Monocytes-CD14+_RO01746	blood

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