Variant report

Variant	rs1060543
Chromosome Location	chr3:156978676-156978677
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs10451916	1.00[CEU][hapmap];0.95[CHB][hapmap];0.91[JPT][hapmap];1.00[YRI][hapmap]
rs1046938	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10513507	1.00[CEU][hapmap];0.83[JPT][hapmap]
rs1157738	0.87[CEU][hapmap]
rs13061214	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs13081036	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs13081038	1.00[CEU][hapmap];0.95[CHB][hapmap];0.91[JPT][hapmap];0.96[YRI][hapmap]
rs1392799	1.00[CEU][hapmap];0.95[CHB][hapmap];0.91[JPT][hapmap];1.00[YRI][hapmap]
rs1403104	0.87[CEU][hapmap]
rs1587535	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs1608127	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs16827308	0.88[CEU][hapmap];0.90[YRI][hapmap]
rs16827322	0.87[CEU][hapmap]
rs3749214	1.00[CEU][hapmap];0.91[CHB][hapmap];0.95[JPT][hapmap];0.96[YRI][hapmap]
rs4679788	0.83[CEU][hapmap]
rs4680342	0.92[CEU][hapmap];0.91[CHB][hapmap];0.91[JPT][hapmap];0.97[YRI][hapmap]
rs4680346	1.00[CEU][hapmap];0.95[CHB][hapmap];0.91[JPT][hapmap];1.00[YRI][hapmap]
rs4680347	0.91[CEU][hapmap]
rs6441123	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs6767619	1.00[CEU][hapmap];0.91[CHB][hapmap];0.91[JPT][hapmap];1.00[YRI][hapmap]
rs6783595	0.92[CEU][hapmap];0.91[CHB][hapmap];0.91[JPT][hapmap];0.87[YRI][hapmap]
rs6805114	0.95[CEU][hapmap];0.95[CHB][hapmap];0.91[JPT][hapmap];0.87[YRI][hapmap]
rs6808457	1.00[CEU][hapmap];0.95[CHB][hapmap];0.91[JPT][hapmap];1.00[YRI][hapmap]
rs6809003	0.92[CEU][hapmap];0.91[CHB][hapmap];0.91[JPT][hapmap];1.00[YRI][hapmap]
rs6809394	0.91[CEU][hapmap];0.91[CHB][hapmap];0.91[JPT][hapmap];0.86[YRI][hapmap]
rs7625059	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs7638194	1.00[CEU][hapmap];0.95[CHB][hapmap];0.91[JPT][hapmap]
rs7647643	1.00[CEU][hapmap];0.95[CHB][hapmap];0.91[JPT][hapmap];1.00[YRI][hapmap]
rs9827676	0.95[CEU][hapmap];0.95[CHB][hapmap];0.91[JPT][hapmap];1.00[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv829766	chr3:156811536-157020551	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	144 gene(s)	inside rSNPs	diseases
2	nsv877687	chr3:156924793-157044184	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:27 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:156967000-156979000	Weak transcription	HSMMtube	muscle
2	chr3:156967200-156982000	Weak transcription	Lung	lung
3	chr3:156967200-156989000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr3:156967200-157000000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr3:156967200-157000000	Weak transcription	NH-A	brain
6	chr3:156967200-157007800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr3:156968000-156981800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr3:156974000-156982400	Weak transcription	Cortex derived primary cultured neurospheres	brain
9	chr3:156974200-156979000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr3:156975200-156979600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
11	chr3:156975200-156980600	Weak transcription	HUES48 Cell Line	embryonic stem cell
12	chr3:156975400-156980600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
13	chr3:156975600-156978800	Weak transcription	HUES64 Cell Line	embryonic stem cell
14	chr3:156975600-156980400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
15	chr3:156975600-156980400	Weak transcription	HUES6 Cell Line	embryonic stem cell
16	chr3:156975600-156980800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr3:156976600-156980400	Weak transcription	HUVEC	blood vessel
18	chr3:156977200-156980600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr3:156977800-156982000	Enhancers	Osteobl	bone
20	chr3:156978000-156979000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr3:156978200-156981600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr3:156978400-156979600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr3:156978400-156980000	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr3:156978400-156981000	Weak transcription	HSMM	muscle
25	chr3:156978400-156981600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr3:156978600-156980000	Enhancers	NHDF-Ad	bronchial
27	chr3:156978600-156981400	Enhancers	Muscle Satellite Cultured Cells	--

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