Variant report

Variant	rs7925086
Chromosome Location	chr11:93401408-93401409
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:93399268..93402269-chr11:93471854..93474833,3	K562	blood:
2	chr11:93399268..93402269-chr11:93473059..93476035,6	K562	blood:
3	chr11:93394628..93397183-chr11:93397951..93402212,5	MCF-7	breast:

Variant related genes	Relation type
ENSG00000166012	Chromatin interaction
ENSG00000166004	Chromatin interaction
ENSG00000182919	Chromatin interaction

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs10741469	0.90[AFR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10765619	0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10765623	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1080367	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];0.86[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10831082	0.95[AFR][1000 genomes];0.96[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10831083	0.95[AFR][1000 genomes];0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10831084	0.81[CEU][hapmap];0.82[CHB][hapmap];0.84[JPT][hapmap];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11020478	0.84[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs11020479	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11529070	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1939568	0.92[CEU][hapmap];0.89[CHB][hapmap];0.83[JPT][hapmap];0.80[AFR][1000 genomes];0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1944108	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];0.82[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2186685	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4363551	0.86[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4376865	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4619111	0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4753485	0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs603360	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];0.83[AFR][1000 genomes];0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs694699	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7111796	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9888134	0.93[EUR][1000 genomes];0.82[ASN][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	nsv898181	chr11:93072843-93662459	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	119 gene(s)	inside rSNPs	diseases
2	nsv898182	chr11:93381845-93637462	Strong transcription Genic enhancers Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	108 gene(s)	inside rSNPs	diseases
3	nsv832232	chr11:93401314-93549438	Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	104 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:93395400-93404000	Weak transcription	Esophagus	oesophagus
2	chr11:93395400-93406400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr11:93395400-93406800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr11:93395400-93406800	Weak transcription	Lung	lung
5	chr11:93395400-93412200	Weak transcription	Gastric	stomach
6	chr11:93395400-93412200	Weak transcription	Pancreas	Pancrea
7	chr11:93395400-93417800	Weak transcription	Small Intestine	intestine
8	chr11:93395600-93402200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
9	chr11:93395600-93403800	Weak transcription	Left Ventricle	heart
10	chr11:93395600-93403800	Weak transcription	Ovary	ovary
11	chr11:93395600-93404000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
12	chr11:93395600-93404200	Weak transcription	Fetal Muscle Leg	muscle
13	chr11:93395600-93408200	Weak transcription	Colon Smooth Muscle	Colon
14	chr11:93395600-93411800	Weak transcription	Aorta	Aorta
15	chr11:93395600-93412200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr11:93395600-93412400	Weak transcription	Skeletal Muscle Male	skeletal muscle
17	chr11:93395600-93412600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr11:93395600-93412600	Weak transcription	Colonic Mucosa	Colon
19	chr11:93395600-93417400	Weak transcription	Stomach Mucosa	stomach
20	chr11:93395600-93446800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
21	chr11:93395800-93411800	Weak transcription	HSMMtube	muscle
22	chr11:93395800-93412200	Weak transcription	Thymus	Thymus
23	chr11:93395800-93413200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr11:93395800-93413400	Weak transcription	Right Ventricle	heart
25	chr11:93395800-93415800	Weak transcription	Rectal Smooth Muscle	rectum
26	chr11:93396200-93404600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
27	chr11:93396200-93411800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
28	chr11:93396400-93401600	Weak transcription	Fetal Brain Female	brain
29	chr11:93396400-93402200	Weak transcription	Primary T cells from cord blood	blood
30	chr11:93396400-93402400	Weak transcription	Brain Inferior Temporal Lobe	brain
31	chr11:93396400-93403800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr11:93396400-93404000	Weak transcription	Fetal Intestine Small	intestine
33	chr11:93396400-93404000	Weak transcription	Fetal Stomach	stomach
34	chr11:93396400-93406400	Weak transcription	Placenta Amnion	Placenta Amnion
35	chr11:93396400-93410400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
36	chr11:93396400-93412200	Weak transcription	Brain Angular Gyrus	brain
37	chr11:93396400-93417600	Weak transcription	Fetal Heart	heart
38	chr11:93396600-93401600	Weak transcription	Brain Germinal Matrix	brain
39	chr11:93396600-93401800	Weak transcription	Rectal Mucosa Donor 31	rectum
40	chr11:93396600-93402200	Weak transcription	Brain Cingulate Gyrus	brain
41	chr11:93396600-93402400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
42	chr11:93396600-93403800	Weak transcription	Cortex derived primary cultured neurospheres	brain
43	chr11:93396600-93403800	Weak transcription	Brain Anterior Caudate	brain
44	chr11:93396600-93407200	Weak transcription	Spleen	Spleen
45	chr11:93396600-93412000	Weak transcription	Psoas Muscle	Psoas
46	chr11:93396600-93413200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr11:93396600-93417600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
48	chr11:93396800-93412600	Weak transcription	A549	lung
49	chr11:93396800-93413200	Weak transcription	NHLF	lung
50	chr11:93396800-93415200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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