Variant report

Variant	rs6874690
Chromosome Location	chr5:59623465-59623466
allele	C/T
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]
rs16877884	0.92[YRI][hapmap]
rs16877888	0.82[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs16877890	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16877893	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16877895	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4460096	0.95[YRI][hapmap];0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57172565	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60693366	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61497235	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6875020	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6891047	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6892680	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73104776	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73104780	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73104781	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73106708	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73106740	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73106742	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73106751	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73106753	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73106756	0.85[AMR][1000 genomes]
rs73106759	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73106769	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73106773	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73106774	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73106777	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7711198	0.83[YRI][hapmap]
rs7712352	0.88[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs7712697	0.84[AFR][1000 genomes];0.87[AMR][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	nsv1025856	chr5:59188419-59928852	Enhancers Strong transcription Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
2	nsv830316	chr5:59480269-59689829	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:59620000-59623600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr5:59620000-59625000	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr5:59620400-59629400	Weak transcription	Aorta	Aorta
4	chr5:59620400-59631000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr5:59623200-59626200	Weak transcription	Placenta Amnion	Placenta Amnion

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