Variant report

Variant	rs8002313
Chromosome Location	chr13:38221869-38221870
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs10400597	1.00[JPT][hapmap]
rs12856733	0.81[CEU][hapmap]
rs12871022	1.00[JPT][hapmap]
rs17256386	1.00[JPT][hapmap]
rs1924289	0.81[CEU][hapmap]
rs2025407	0.81[CEU][hapmap]
rs2147124	0.81[CEU][hapmap]
rs2274082	1.00[JPT][hapmap]
rs2957208	1.00[JPT][hapmap]
rs2957214	0.81[CEU][hapmap]
rs2957215	0.81[CEU][hapmap]
rs2957218	0.81[CEU][hapmap]
rs2985159	1.00[JPT][hapmap]
rs2985170	0.80[CEU][hapmap]
rs3794374	1.00[JPT][hapmap]
rs4142596	1.00[JPT][hapmap]
rs4390468	1.00[JPT][hapmap]
rs4450268	0.81[CEU][hapmap]
rs7317546	0.92[CEU][hapmap]
rs7322993	1.00[JPT][hapmap]
rs7336008	0.81[CEU][hapmap]
rs7337173	0.81[CEU][hapmap]
rs7337477	0.81[CEU][hapmap]
rs7338239	0.81[CEU][hapmap]
rs8000073	1.00[JPT][hapmap]
rs9315503	1.00[JPT][hapmap]
rs9566245	0.81[CEU][hapmap]
rs9566246	0.81[CEU][hapmap]
rs9566247	0.81[CEU][hapmap]
rs9566248	0.81[CEU][hapmap]
rs9566249	0.81[CEU][hapmap]
rs9576307	1.00[JPT][hapmap]
rs9576309	1.00[JPT][hapmap]
rs9576313	1.00[JPT][hapmap]
rs9576314	1.00[JPT][hapmap]
rs9576328	0.81[CEU][hapmap];1.00[JPT][hapmap]
rs9576329	0.81[CEU][hapmap]
rs9576332	0.81[CEU][hapmap]
rs9594224	0.81[CEU][hapmap]
rs9594226	0.81[CEU][hapmap]
rs9603244	0.84[CEU][hapmap]
rs9603245	0.81[CEU][hapmap]
rs9603246	0.81[CEU][hapmap]

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	nsv948975	chr13:37281203-38280430	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
2	esv34109	chr13:37843819-38276391	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
3	nsv1045716	chr13:37952062-38394595	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Active TSS Bivalent Enhancer 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	nsv915901	chr13:38199035-39032633	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:28 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:38207600-38224000	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr13:38211400-38275600	Weak transcription	Stomach Smooth Muscle	stomach
3	chr13:38219600-38230600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr13:38219800-38222400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr13:38219800-38223600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr13:38219800-38224400	Weak transcription	Fetal Brain Male	brain
7	chr13:38220000-38222000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr13:38220000-38222400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr13:38220400-38224200	Weak transcription	Placenta	Placenta
10	chr13:38220600-38222000	Enhancers	HUVEC	blood vessel
11	chr13:38220800-38222000	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr13:38221000-38222000	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr13:38221000-38223400	Enhancers	Hela-S3	cervix
14	chr13:38221200-38222000	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr13:38221200-38223200	Enhancers	NHDF-Ad	bronchial
16	chr13:38221200-38223600	Enhancers	Osteobl	bone
17	chr13:38221400-38222000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
18	chr13:38221600-38222000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr13:38221600-38226600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr13:38221600-38226800	Weak transcription	NH-A	brain
21	chr13:38221600-38228200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr13:38221600-38228200	Weak transcription	Pancreatic Islets	Pancreatic Islet
23	chr13:38221600-38239600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
24	chr13:38221800-38222200	Weak transcription	Muscle Satellite Cultured Cells	--
25	chr13:38221800-38222800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr13:38221800-38231400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr13:38221800-38233200	Weak transcription	Ovary	ovary
28	chr13:38221800-38239400	Weak transcription	iPS-18 Cell Line	embryonic stem cell

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