Variant report

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs10076374	0.96[EUR][1000 genomes]
rs13157757	1.00[EUR][1000 genomes]
rs13167694	0.85[EUR][1000 genomes]
rs13167816	0.85[EUR][1000 genomes]
rs1598817	0.93[EUR][1000 genomes]
rs17152731	1.00[MEX][hapmap]
rs2220621	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59771425	0.85[EUR][1000 genomes]
rs60163815	0.81[EUR][1000 genomes]
rs60696888	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61202049	0.81[EUR][1000 genomes]
rs62373366	0.85[EUR][1000 genomes]
rs62373367	0.85[EUR][1000 genomes]
rs62373368	0.85[EUR][1000 genomes]
rs62373384	0.85[EUR][1000 genomes]
rs62373385	0.85[EUR][1000 genomes]
rs62373387	0.92[EUR][1000 genomes]
rs62373389	0.92[EUR][1000 genomes]
rs62373391	0.93[EUR][1000 genomes]
rs62373392	1.00[EUR][1000 genomes]
rs62373412	1.00[EUR][1000 genomes]
rs62373414	0.96[EUR][1000 genomes]
rs6899200	0.81[EUR][1000 genomes]
rs7710810	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7717300	0.96[EUR][1000 genomes]

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	nsv1030992	chr5:124708549-125391503	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv537892	chr5:124708549-125391503	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	nsv882827	chr5:124867823-124943901	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
4	nsv882828	chr5:124867823-124958205	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:124884200-124895600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr5:124884800-124889000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr5:124884800-124889000	Enhancers	NHLF	lung
4	chr5:124885200-124888200	Enhancers	Placenta Amnion	Placenta Amnion
5	chr5:124885800-124889000	Enhancers	Muscle Satellite Cultured Cells	--
6	chr5:124885800-124889000	Enhancers	HUVEC	blood vessel
7	chr5:124886000-124889200	Weak transcription	Pancreatic Islets	Pancreatic Islet
8	chr5:124886400-124888000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr5:124886400-124888400	Weak transcription	Osteobl	bone
10	chr5:124887200-124888600	Enhancers	HSMM	muscle
11	chr5:124887400-124889200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr5:124887400-124893800	Weak transcription	NH-A	brain
13	chr5:124887400-124894400	Weak transcription	Fetal Lung	lung
14	chr5:124887400-124894800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr5:124887600-124889200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr5:124887800-124888000	Enhancers	Fetal Kidney	kidney
17	chr5:124887800-124888600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr5:124887800-124889000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr5:124887800-124894200	Weak transcription	NHDF-Ad	bronchial

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