Variant report

Variant	rs9645703
Chromosome Location	chr11:86259864-86259865
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs1006586	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs1006587	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs10444371	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.81[GIH][hapmap];1.00[JPT][hapmap];0.85[MEX][hapmap];0.90[MKK][hapmap];0.94[TSI][hapmap];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10444372	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.81[GIH][hapmap];1.00[JPT][hapmap];0.86[MEX][hapmap];0.90[MKK][hapmap];0.94[TSI][hapmap];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10444373	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10444374	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10501622	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.87[MKK][hapmap];1.00[ASN][1000 genomes]
rs10898488	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10898494	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10898495	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11234643	1.00[CHB][hapmap];0.83[JPT][hapmap]
rs11234668	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs11234684	0.98[EUR][1000 genomes]
rs12361416	0.94[ASN][1000 genomes]
rs12362900	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12420965	1.00[CHB][hapmap]
rs12421147	1.00[ASN][1000 genomes]
rs12791972	0.83[ASN][1000 genomes]
rs12792300	0.94[ASN][1000 genomes]
rs12793707	1.00[ASN][1000 genomes]
rs12799562	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs12808738	0.83[ASN][1000 genomes]
rs17149169	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs28895937	1.00[ASN][1000 genomes]
rs34405620	0.90[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs35042210	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3758877	1.00[CHB][hapmap]
rs3758878	1.00[CHB][hapmap]
rs3824952	1.00[CHB][hapmap];0.91[JPT][hapmap]
rs628449	0.91[CEU][hapmap];1.00[CHB][hapmap];0.83[JPT][hapmap]
rs7112309	1.00[CHB][hapmap]
rs72953626	1.00[ASN][1000 genomes]
rs7926965	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs7944836	1.00[CHB][hapmap];0.91[JPT][hapmap];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 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
4	nsv555665	chr11:86230898-86417553	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:71 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:86237800-86262200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr11:86249800-86261800	Weak transcription	Rectal Mucosa Donor 31	rectum
3	chr11:86250400-86261600	Weak transcription	Gastric	stomach
4	chr11:86251200-86261600	Weak transcription	Right Ventricle	heart
5	chr11:86256600-86262400	Weak transcription	Primary hematopoietic stem cells	blood
6	chr11:86257800-86262200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr11:86258600-86261000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr11:86258800-86260000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr11:86258800-86260000	Enhancers	Muscle Satellite Cultured Cells	--
10	chr11:86258800-86260000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr11:86258800-86260000	Enhancers	Fetal Kidney	kidney
12	chr11:86258800-86260000	Enhancers	Fetal Muscle Leg	muscle
13	chr11:86258800-86260000	Enhancers	Fetal Stomach	stomach
14	chr11:86258800-86260000	Enhancers	Skeletal Muscle Male	skeletal muscle
15	chr11:86258800-86260000	Enhancers	HMEC	breast
16	chr11:86258800-86260200	Enhancers	Adipose Nuclei	Adipose
17	chr11:86258800-86260200	Enhancers	Brain Anterior Caudate	brain
18	chr11:86258800-86260200	Enhancers	NHEK	skin
19	chr11:86258800-86260400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr11:86258800-86260400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr11:86258800-86260400	Enhancers	Aorta	Aorta
22	chr11:86258800-86260800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr11:86258800-86260800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr11:86258800-86260800	Enhancers	NHDF-Ad	bronchial
25	chr11:86258800-86260800	Enhancers	NHLF	lung
26	chr11:86258800-86261000	Enhancers	Breast Myoepithelial Primary Cells	Breast
27	chr11:86258800-86261000	Enhancers	Fetal Brain Female	brain
28	chr11:86258800-86261200	Enhancers	NH-A	brain
29	chr11:86258800-86262200	Enhancers	HUVEC	blood vessel
30	chr11:86258800-86263400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
31	chr11:86258800-86263400	Enhancers	Fetal Brain Male	brain
32	chr11:86258800-86263400	Enhancers	Psoas Muscle	Psoas
33	chr11:86258800-86264600	Enhancers	Right Atrium	heart
34	chr11:86259000-86260000	Enhancers	Colon Smooth Muscle	Colon
35	chr11:86259000-86260000	Enhancers	Duodenum Smooth Muscle	Duodenum
36	chr11:86259000-86260000	Enhancers	Left Ventricle	heart
37	chr11:86259000-86260000	Enhancers	Pancreas	Pancrea
38	chr11:86259000-86260000	Enhancers	Stomach Mucosa	stomach
39	chr11:86259000-86260000	Enhancers	HSMMtube	muscle
40	chr11:86259000-86260400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr11:86259000-86260400	Enhancers	Placenta Amnion	Placenta Amnion
42	chr11:86259000-86261400	Enhancers	Osteobl	bone
43	chr11:86259000-86263200	Weak transcription	Brain Germinal Matrix	brain
44	chr11:86259200-86260000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr11:86259200-86260000	Weak transcription	Fetal Intestine Small	intestine
46	chr11:86259200-86261400	Weak transcription	Lung	lung
47	chr11:86259200-86262200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr11:86259200-86262200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
49	chr11:86259200-86262400	Weak transcription	Ovary	ovary
50	chr11:86259200-86264400	Weak transcription	Fetal Muscle Trunk	muscle

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