Variant report

Variant	rs10840333
Chromosome Location	chr11:9981768-9981769
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 95 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:91)

rs_ID	r²[population]
rs10500715	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs10500717	0.86[CHB][hapmap];1.00[JPT][hapmap]
rs10743123	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10770077	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10770078	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10770079	0.86[CHB][hapmap];1.00[JPT][hapmap]
rs10840327	0.85[CEU][hapmap]
rs10840330	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10840334	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[YRI][hapmap];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10840337	0.90[CEU][hapmap];0.88[EUR][1000 genomes]
rs10840338	0.90[CEU][hapmap];0.89[EUR][1000 genomes]
rs10840347	0.86[CHB][hapmap];1.00[JPT][hapmap]
rs10840348	0.86[CHB][hapmap];1.00[JPT][hapmap]
rs10840359	0.83[EUR][1000 genomes]
rs10840361	0.86[CHB][hapmap];1.00[JPT][hapmap]
rs10840362	0.86[CHB][hapmap];1.00[JPT][hapmap]
rs10840370	0.86[CHB][hapmap];0.93[JPT][hapmap]
rs11042543	0.80[CEU][hapmap]
rs11042558	0.91[ASN][1000 genomes]
rs11042559	0.86[CEU][hapmap];0.88[EUR][1000 genomes]
rs11042561	0.90[CEU][hapmap];0.89[EUR][1000 genomes]
rs11042571	0.89[EUR][1000 genomes]
rs11042573	0.82[EUR][1000 genomes]
rs11042574	0.86[CHB][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs11042578	0.88[EUR][1000 genomes]
rs11042579	0.90[CEU][hapmap];0.87[EUR][1000 genomes]
rs11042580	0.86[EUR][1000 genomes]
rs11042589	0.93[CHB][hapmap];1.00[JPT][hapmap]
rs11042590	0.93[CHB][hapmap];1.00[JPT][hapmap]
rs11042591	0.93[CHB][hapmap];1.00[JPT][hapmap]
rs11042595	0.85[CEU][hapmap]
rs11042601	0.85[CEU][hapmap]
rs11042604	0.86[CHB][hapmap];1.00[JPT][hapmap]
rs11042605	0.86[CHB][hapmap];1.00[JPT][hapmap]
rs11042609	0.85[CEU][hapmap]
rs11042613	0.86[CHB][hapmap];0.93[JPT][hapmap]
rs11042615	0.86[CEU][hapmap]
rs11042618	0.85[CEU][hapmap]
rs11042623	0.83[CEU][hapmap]
rs11042624	0.86[CHB][hapmap];0.93[JPT][hapmap]
rs11042632	0.89[CEU][hapmap]
rs11042639	0.86[CHB][hapmap];0.93[JPT][hapmap]
rs11042645	1.00[JPT][hapmap]
rs11600251	0.86[CEU][hapmap]
rs11602465	0.88[EUR][1000 genomes]
rs11602515	0.86[CEU][hapmap]
rs11603440	0.87[EUR][1000 genomes]
rs11606561	0.86[CEU][hapmap]
rs12222953	0.93[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs12283105	1.00[JPT][hapmap]
rs12290996	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12419923	0.90[CEU][hapmap];0.89[EUR][1000 genomes]
rs12420734	0.89[CEU][hapmap]
rs12420950	0.84[EUR][1000 genomes]
rs12421096	0.85[CEU][hapmap]
rs12421200	0.90[CEU][hapmap];0.90[EUR][1000 genomes]
rs12575719	0.86[CHB][hapmap];1.00[JPT][hapmap]
rs1372807	0.95[CEU][hapmap];0.87[CHB][hapmap];0.85[JPT][hapmap];0.80[EUR][1000 genomes]
rs1442732	0.86[CHB][hapmap];1.00[JPT][hapmap]
rs16907368	0.93[CHB][hapmap];1.00[JPT][hapmap]
rs16907396	0.93[CHB][hapmap];0.93[JPT][hapmap]
rs17271847	0.90[CEU][hapmap];0.89[EUR][1000 genomes]
rs17356792	0.90[CEU][hapmap];0.89[EUR][1000 genomes]
rs2403226	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2403227	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2403229	1.00[CEU][hapmap];0.93[CHB][hapmap];0.86[JPT][hapmap];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4478985	0.81[EUR][1000 genomes]
rs4529876	0.82[EUR][1000 genomes]
rs4576815	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4625455	0.95[CEU][hapmap];0.93[CHB][hapmap];0.93[JPT][hapmap]
rs4909915	0.86[CEU][hapmap]
rs4909917	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.81[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4910080	0.82[CEU][hapmap]
rs4910081	0.85[CEU][hapmap]
rs4910086	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs58084362	0.89[ASN][1000 genomes]
rs60362241	0.89[ASN][1000 genomes]
rs7106914	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs7114044	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7114303	0.95[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.81[EUR][1000 genomes]
rs7123453	0.85[CEU][hapmap]
rs7131445	0.90[CEU][hapmap];0.89[EUR][1000 genomes]
rs7928959	0.86[CEU][hapmap]
rs7933475	0.97[ASN][1000 genomes]
rs7938491	0.85[CEU][hapmap]
rs7938502	0.86[CEU][hapmap]
rs7938647	0.85[CEU][hapmap]
rs7938788	0.95[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.80[EUR][1000 genomes]
rs7946995	0.92[CHB][hapmap];0.93[JPT][hapmap];0.84[YRI][hapmap];0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7950447	0.85[CEU][hapmap]
rs7951950	0.99[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	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	nsv896988	chr11:9912052-10012511	Strong transcription Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv896989	chr11:9951968-10059623	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
4	esv1819684	chr11:9973062-10012511	Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Enhancers Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:102 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:9952800-9995200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr11:9968000-9984000	Weak transcription	Primary B cells from cord blood	blood
3	chr11:9968000-9984200	Weak transcription	Fetal Kidney	kidney
4	chr11:9973000-9986000	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr11:9973800-10010600	Weak transcription	Fetal Brain Male	brain
6	chr11:9974200-9994400	Weak transcription	HUES48 Cell Line	embryonic stem cell
7	chr11:9974200-9994600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr11:9974200-9994800	Weak transcription	HUES6 Cell Line	embryonic stem cell
9	chr11:9974200-9999000	Weak transcription	Fetal Heart	heart
10	chr11:9974200-9999000	Weak transcription	HSMMtube	muscle
11	chr11:9974400-9982800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr11:9975400-9985600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr11:9977000-9994400	Weak transcription	Muscle Satellite Cultured Cells	--
14	chr11:9977600-9982000	Weak transcription	Stomach Mucosa	stomach
15	chr11:9978600-9981800	Strong transcription	Left Ventricle	heart
16	chr11:9978600-9986000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr11:9978800-9985000	Weak transcription	Small Intestine	intestine
18	chr11:9979400-9982000	Weak transcription	Colonic Mucosa	Colon
19	chr11:9979400-9986000	Strong transcription	Monocytes-CD14+_RO01746	blood
20	chr11:9979400-9995000	Weak transcription	Pancreatic Islets	Pancreatic Islet
21	chr11:9979600-9981800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
22	chr11:9979600-9982000	Strong transcription	Fetal Stomach	stomach
23	chr11:9979600-9985600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr11:9979600-9985800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr11:9979600-9994600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
26	chr11:9979800-9987400	Weak transcription	Primary T helper cells fromperipheralblood	blood
27	chr11:9979800-9999200	Weak transcription	NH-A	brain
28	chr11:9980000-9982200	Weak transcription	Thymus	Thymus
29	chr11:9980200-9981800	Strong transcription	Cortex derived primary cultured neurospheres	brain
30	chr11:9980200-9981800	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr11:9980200-9981800	Strong transcription	Ovary	ovary
32	chr11:9980200-9982000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr11:9980200-9983000	Strong transcription	Fetal Brain Female	brain
34	chr11:9980200-9983800	Strong transcription	Adipose Nuclei	Adipose
35	chr11:9980200-9984800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr11:9980200-9985800	Strong transcription	Liver	Liver
37	chr11:9980200-9985800	Strong transcription	Placenta	Placenta
38	chr11:9980200-9986000	Strong transcription	Primary monocytes fromperipheralblood	blood
39	chr11:9980400-9981800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr11:9980400-9981800	Strong transcription	Brain Inferior Temporal Lobe	brain
41	chr11:9980400-9981800	Strong transcription	Skeletal Muscle Male	skeletal muscle
42	chr11:9980400-9983400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr11:9981000-9983400	Weak transcription	Rectal Mucosa Donor 31	rectum
44	chr11:9981000-10020000	Weak transcription	Sigmoid Colon	Sigmoid Colon
45	chr11:9981200-9982600	Weak transcription	Osteobl	bone
46	chr11:9981200-9983200	Weak transcription	NHDF-Ad	bronchial
47	chr11:9981200-9984400	Weak transcription	H1 Cell Line	embryonic stem cell
48	chr11:9981200-9988400	Weak transcription	HMEC	breast
49	chr11:9981200-9990000	Weak transcription	A549	lung
50	chr11:9981200-9990600	Weak transcription	iPS-18 Cell Line	embryonic stem cell

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