Variant report

Variant	rs55791846
Chromosome Location	chr15:54936710-54936711
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 55 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs13379714	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16974912	1.00[AMR][1000 genomes]
rs16974918	1.00[AMR][1000 genomes]
rs16974964	1.00[AMR][1000 genomes]
rs16974972	1.00[AMR][1000 genomes]
rs2681968	1.00[AMR][1000 genomes]
rs2681971	1.00[AMR][1000 genomes]
rs55864386	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57172973	1.00[AMR][1000 genomes]
rs58775812	1.00[AMR][1000 genomes]
rs58942353	1.00[AMR][1000 genomes]
rs59258545	1.00[AMR][1000 genomes]
rs60233308	1.00[AMR][1000 genomes]
rs60820899	1.00[AMR][1000 genomes]
rs60910499	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61298021	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73407659	1.00[AMR][1000 genomes]
rs73407663	1.00[AMR][1000 genomes]
rs73409746	1.00[AMR][1000 genomes]
rs73409748	1.00[AMR][1000 genomes]
rs74014204	1.00[AMR][1000 genomes]
rs74014255	1.00[AMR][1000 genomes]
rs74014260	1.00[AMR][1000 genomes]
rs74014261	1.00[AMR][1000 genomes]
rs74014263	1.00[AMR][1000 genomes]
rs74014269	1.00[AMR][1000 genomes]
rs74014270	1.00[AMR][1000 genomes]
rs74014272	1.00[AMR][1000 genomes]
rs74014273	1.00[AMR][1000 genomes]
rs74014274	1.00[AMR][1000 genomes]
rs74014277	1.00[AMR][1000 genomes]
rs74014278	1.00[AMR][1000 genomes]
rs74014284	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74014285	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74014286	0.97[AFR][1000 genomes]
rs74014287	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74014288	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74014290	1.00[AMR][1000 genomes]
rs74014291	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74014292	1.00[AMR][1000 genomes]
rs74014293	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74014294	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74014295	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74014296	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74014298	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74016813	1.00[AMR][1000 genomes]
rs8040563	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv817539	chr15:54132584-55095235	Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
2	nsv1038660	chr15:54756184-55039913	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
3	nsv569518	chr15:54898631-54954864	Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA miRNA target site	1 gene(s)	inside rSNPs	diseases
4	nsv1043600	chr15:54910593-55010156	Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats	Chromatin interactive region miRNA target site	n/a	inside rSNPs	diseases
5	nsv1043237	chr15:54916301-55034633	Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region miRNA target site	n/a	inside rSNPs	diseases
6	nsv904238	chr15:54919539-54998764	Enhancers Active TSS Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region miRNA target site	n/a	inside rSNPs	diseases
7	nsv1053983	chr15:54920850-54999183	Enhancers Active TSS ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv833013	chr15:54927825-55135274	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:54934200-54938000	Weak transcription	Aorta	Aorta

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