Variant report

Variant	rs2199790
Chromosome Location	chr14:79601834-79601835
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs10137386	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2127452	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2170046	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2219847	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2620392	1.00[AMR][1000 genomes]
rs2620393	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2620394	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2653544	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2653546	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2653547	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2653548	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2653549	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2653550	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2653551	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2653553	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2653554	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7156708	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1041991	chr14:79394408-79644886	Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv931412	chr14:79420297-79928269	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv948724	chr14:79484233-79614043	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	esv2761846	chr14:79522198-79629157	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv1040837	chr14:79583862-79711565	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:79601000-79602800	Weak transcription	Brain Germinal Matrix	brain
2	chr14:79601600-79602600	Weak transcription	Brain Anterior Caudate	brain

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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