Variant report

Variant	rs17466633
Chromosome Location	chr12:40760749-40760750
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs11564113	1.00[JPT][hapmap]
rs11613829	1.00[JPT][hapmap]
rs17443421	1.00[JPT][hapmap]
rs17443552	1.00[JPT][hapmap]
rs17444103	1.00[JPT][hapmap]
rs17444542	1.00[JPT][hapmap]
rs17465716	1.00[JPT][hapmap]
rs17465849	1.00[JPT][hapmap]
rs17465891	1.00[JPT][hapmap]
rs17466030	1.00[JPT][hapmap]
rs17466220	1.00[JPT][hapmap]
rs17466269	1.00[JPT][hapmap]
rs17466297	1.00[JPT][hapmap]
rs17466339	1.00[JPT][hapmap]
rs17466451	1.00[JPT][hapmap]
rs17466556	1.00[JPT][hapmap]
rs17490578	1.00[JPT][hapmap]
rs17490620	1.00[JPT][hapmap]
rs17490762	1.00[JPT][hapmap]
rs17491110	1.00[JPT][hapmap]
rs17491410	1.00[JPT][hapmap]
rs17492138	1.00[JPT][hapmap]
rs17519797	1.00[JPT][hapmap]
rs17520634	1.00[JPT][hapmap]
rs17520655	1.00[JPT][hapmap]
rs28365202	1.00[JPT][hapmap]
rs28365243	1.00[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1044685	chr12:40574460-40771612	Enhancers ZNF genes & repeats Bivalent/Poised TSS Active TSS Strong transcription Flanking Active TSS Weak transcription 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	9 gene(s)	inside rSNPs	diseases
2	nsv832377	chr12:40704881-40855223	Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
3	nsv899032	chr12:40735939-40827479	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
4	nsv558598	chr12:40742363-40828264	Strong transcription Weak transcription Enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
5	nsv899033	chr12:40758652-41122288	Bivalent/Poised TSS Enhancers Strong transcription Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:24 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:40640600-40768200	Weak transcription	Pancreas	Pancrea
2	chr12:40681200-40763000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr12:40687200-40765000	Strong transcription	Primary neutrophils fromperipheralblood	blood
4	chr12:40716800-40761600	Weak transcription	Fetal Kidney	kidney
5	chr12:40725200-40761200	Weak transcription	Psoas Muscle	Psoas
6	chr12:40726200-40766600	Weak transcription	A549	lung
7	chr12:40726200-40767800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr12:40732800-40764000	Weak transcription	Colon Smooth Muscle	Colon
9	chr12:40733600-40761400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
10	chr12:40747200-40762400	Strong transcription	Primary B cells from peripheral blood	blood
11	chr12:40747800-40765000	Strong transcription	Monocytes-CD14+_RO01746	blood
12	chr12:40747800-40765200	Strong transcription	Primary monocytes fromperipheralblood	blood
13	chr12:40751400-40762600	Strong transcription	Liver	Liver
14	chr12:40751800-40763600	Weak transcription	Brain Anterior Caudate	brain
15	chr12:40754000-40762000	Strong transcription	Primary B cells from cord blood	blood
16	chr12:40754800-40764000	Weak transcription	Esophagus	oesophagus
17	chr12:40754800-40765600	Weak transcription	Aorta	Aorta
18	chr12:40754800-40767600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
19	chr12:40755800-40761600	Weak transcription	Stomach Smooth Muscle	stomach
20	chr12:40756000-40763600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr12:40758200-40765600	Weak transcription	Adipose Nuclei	Adipose
22	chr12:40759000-40765200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr12:40759200-40764000	Weak transcription	Skeletal Muscle Female	skeletal muscle
24	chr12:40760000-40765600	Weak transcription	Duodenum Smooth Muscle	Duodenum

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