Variant report

Variant	rs11033738
Chromosome Location	chr11:36676453-36676454
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 39 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs10219403	0.83[AFR][1000 genomes]
rs11033704	0.91[YRI][hapmap];0.83[AFR][1000 genomes]
rs11033705	0.91[YRI][hapmap];0.83[AFR][1000 genomes]
rs11033726	1.00[YRI][hapmap]
rs11033739	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11033740	0.81[AFR][1000 genomes]
rs11033754	0.80[AFR][1000 genomes]
rs11033791	1.00[AMR][1000 genomes]
rs11820706	0.81[AFR][1000 genomes]
rs11825620	0.91[YRI][hapmap]
rs12270782	1.00[AMR][1000 genomes]
rs12271279	1.00[YRI][hapmap]
rs12271312	1.00[YRI][hapmap];0.83[AFR][1000 genomes]
rs12272250	1.00[AMR][1000 genomes]
rs12272928	0.81[AFR][1000 genomes]
rs12273796	0.88[YRI][hapmap];0.81[AFR][1000 genomes]
rs12274720	0.81[AFR][1000 genomes]
rs12277409	1.00[AMR][1000 genomes]
rs12277745	0.90[YRI][hapmap]
rs12281063	1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12282321	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12283026	0.91[YRI][hapmap];0.81[AFR][1000 genomes]
rs12294126	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13377317	1.00[YRI][hapmap];0.83[AFR][1000 genomes]
rs35211174	0.81[AFR][1000 genomes]
rs4150999	0.89[YRI][hapmap]
rs4151001	1.00[YRI][hapmap];0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4151030	0.91[YRI][hapmap]
rs4151047	0.91[YRI][hapmap]
rs7119565	0.83[AFR][1000 genomes]
rs7949264	1.00[YRI][hapmap]
rs9971624	0.81[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv467791	chr11:36108497-36999385	Flanking Active TSS Weak transcription Strong transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
2	nsv554003	chr11:36108497-36999385	ZNF genes & repeats Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
3	nsv832123	chr11:36582872-36757443	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
4	nsv467792	chr11:36624187-36898373	ZNF genes & repeats Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv554005	chr11:36624187-36898373	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv467793	chr11:36632515-37171833	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	nsv554006	chr11:36632515-37171833	Active TSS Enhancers Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs11033738	LOC119710	cis	multi-tissue	Pritchard
rs11033738	C11orf74	cis	multi-tissue	Pritchard

Chromatin state (count:48 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:36630000-36678800	Weak transcription	Brain Angular Gyrus	brain
2	chr11:36630600-36682000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
3	chr11:36641400-36681000	Weak transcription	Primary T cells from cord blood	blood
4	chr11:36642000-36681000	Weak transcription	Fetal Kidney	kidney
5	chr11:36646400-36677000	Weak transcription	Lung	lung
6	chr11:36648600-36681400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr11:36648800-36680600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr11:36650600-36687000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr11:36650800-36682600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr11:36651000-36684000	Weak transcription	HSMMtube	muscle
11	chr11:36653600-36680800	Weak transcription	Brain Anterior Caudate	brain
12	chr11:36653800-36684400	Weak transcription	Brain Inferior Temporal Lobe	brain
13	chr11:36656400-36680600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr11:36656800-36677800	Weak transcription	Psoas Muscle	Psoas
15	chr11:36660800-36685800	Weak transcription	Fetal Stomach	stomach
16	chr11:36661200-36678600	Weak transcription	Fetal Thymus	thymus
17	chr11:36661400-36681200	Weak transcription	Gastric	stomach
18	chr11:36661600-36681200	Weak transcription	Colon Smooth Muscle	Colon
19	chr11:36666800-36679000	Weak transcription	Spleen	Spleen
20	chr11:36666800-36692800	Weak transcription	Fetal Heart	heart
21	chr11:36667400-36680800	Weak transcription	Sigmoid Colon	Sigmoid Colon
22	chr11:36668000-36683800	Weak transcription	Brain Germinal Matrix	brain
23	chr11:36668200-36680600	Weak transcription	Fetal Intestine Large	intestine
24	chr11:36668200-36680800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr11:36668200-36681000	Weak transcription	Brain Hippocampus Middle	brain
26	chr11:36669600-36680600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr11:36669800-36678400	Weak transcription	Aorta	Aorta
28	chr11:36669800-36685600	Weak transcription	Fetal Muscle Leg	muscle
29	chr11:36670200-36682600	Weak transcription	Brain Cingulate Gyrus	brain
30	chr11:36670600-36680600	Weak transcription	Duodenum Smooth Muscle	Duodenum
31	chr11:36670600-36680600	Weak transcription	Fetal Lung	lung
32	chr11:36670600-36680600	Weak transcription	Stomach Smooth Muscle	stomach
33	chr11:36670600-36680800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr11:36670600-36680800	Weak transcription	Left Ventricle	heart
35	chr11:36670600-36680800	Weak transcription	Ovary	ovary
36	chr11:36670600-36682800	Weak transcription	Skeletal Muscle Female	skeletal muscle
37	chr11:36670800-36680800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr11:36670800-36683600	Weak transcription	Skeletal Muscle Male	skeletal muscle
39	chr11:36671000-36680600	Weak transcription	Adipose Nuclei	Adipose
40	chr11:36671000-36683800	Weak transcription	Fetal Muscle Trunk	muscle
41	chr11:36671800-36680600	Weak transcription	Liver	Liver
42	chr11:36671800-36681400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr11:36672000-36679000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr11:36672000-36680600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
45	chr11:36674600-36678800	Weak transcription	Thymus	Thymus
46	chr11:36675800-36678800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr11:36675800-36680600	Weak transcription	Primary hematopoietic stem cells	blood
48	chr11:36676400-36677200	Strong transcription	Primary hematopoietic stem cells short term culture	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links