Variant report

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs12249686	1.00[EUR][1000 genomes]
rs12249754	1.00[EUR][1000 genomes]
rs12257401	1.00[EUR][1000 genomes]
rs12261280	1.00[EUR][1000 genomes]
rs12264364	1.00[EUR][1000 genomes]
rs12264374	1.00[EUR][1000 genomes]
rs12264432	1.00[EUR][1000 genomes]
rs16914038	1.00[EUR][1000 genomes]
rs16914371	1.00[EUR][1000 genomes]
rs2090120	1.00[EUR][1000 genomes]
rs2393568	1.00[EUR][1000 genomes]
rs28406036	1.00[EUR][1000 genomes]
rs2893810	1.00[EUR][1000 genomes]
rs2893811	1.00[EUR][1000 genomes]
rs4275570	1.00[EUR][1000 genomes]
rs7073222	1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7077386	1.00[EUR][1000 genomes]
rs7475333	1.00[EUR][1000 genomes]
rs7898886	0.81[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs7917618	1.00[EUR][1000 genomes]

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	esv3347621	chr10:61490062-61527578	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	esv3427654	chr10:61491530-61526282	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:61494600-61495200	Enhancers	Fetal Intestine Large	intestine
2	chr10:61494600-61495200	Enhancers	Psoas Muscle	Psoas
3	chr10:61494600-61495600	Enhancers	Fetal Intestine Small	intestine
4	chr10:61494800-61495000	Weak transcription	Skeletal Muscle Male	skeletal muscle
5	chr10:61494800-61495400	Enhancers	Stomach Mucosa	stomach
6	chr10:61494800-61495800	Enhancers	HepG2	liver
7	chr10:61494800-61496000	Enhancers	Pancreatic Islets	Pancreatic Islet
8	chr10:61494800-61497600	Weak transcription	Skeletal Muscle Female	skeletal muscle

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