Variant report

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs1017439	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1370160	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs1370161	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[YRI][hapmap]
rs1436941	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap]
rs1816567	0.89[CEU][hapmap]
rs1821794	0.89[CEU][hapmap]
rs1836986	1.00[CEU][hapmap];1.00[CHB][hapmap];0.83[JPT][hapmap];0.86[YRI][hapmap]
rs1836988	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap]
rs1987384	0.86[YRI][hapmap]
rs2083008	0.80[CHB][hapmap];0.88[YRI][hapmap]
rs2118172	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap]
rs3821725	1.00[CEU][hapmap];1.00[CHB][hapmap];0.82[JPT][hapmap];0.83[YRI][hapmap]
rs4328836	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4928058	0.83[YRI][hapmap]
rs4928093	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6778625	0.89[CEU][hapmap]
rs6786325	1.00[CEU][hapmap];1.00[CHB][hapmap];0.83[YRI][hapmap]
rs6786332	1.00[CEU][hapmap];0.93[CHB][hapmap];0.90[YRI][hapmap]
rs9290245	0.89[CEU][hapmap]
rs975536	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9878937	0.84[CEU][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	nsv514163	chr3:100547342-100670846	Flanking Active TSS Genic enhancers Enhancers Weak transcription Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv931417	chr3:100547347-101183844	Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:100594400-100618200	Weak transcription	Rectal Smooth Muscle	rectum
2	chr3:100594600-100616800	Weak transcription	Ovary	ovary
3	chr3:100598600-100612400	Weak transcription	Colon Smooth Muscle	Colon
4	chr3:100599600-100610400	Weak transcription	Fetal Muscle Leg	muscle
5	chr3:100599600-100645400	Weak transcription	Duodenum Smooth Muscle	Duodenum
6	chr3:100599800-100610600	Weak transcription	Fetal Stomach	stomach
7	chr3:100599800-100618200	Weak transcription	Fetal Lung	lung
8	chr3:100600000-100610400	Weak transcription	Stomach Smooth Muscle	stomach
9	chr3:100600200-100610200	Weak transcription	Muscle Satellite Cultured Cells	--
10	chr3:100600200-100610400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr3:100602000-100603600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr3:100602000-100609200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr3:100602200-100610200	Weak transcription	Osteobl	bone
14	chr3:100602200-100616800	Weak transcription	NHDF-Ad	bronchial
15	chr3:100602400-100606600	Weak transcription	Hela-S3	cervix
16	chr3:100603400-100604200	Strong transcription	Fetal Muscle Trunk	muscle
17	chr3:100603400-100604400	Strong transcription	HSMMtube	muscle
18	chr3:100603400-100608000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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