Variant report

Variant	rs2676178
Chromosome Location	chr15:56851495-56851496
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 50 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs10518855	0.88[EUR][1000 genomes]
rs10518872	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs1087705	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11071285	1.00[CEU][hapmap];0.94[EUR][1000 genomes]
rs12438728	1.00[CEU][hapmap];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12439116	1.00[CEU][hapmap];0.94[EUR][1000 genomes]
rs12439563	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12439586	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12440006	0.97[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12441746	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12443178	0.94[EUR][1000 genomes]
rs12903143	0.94[EUR][1000 genomes]
rs12907983	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1364541	0.85[EUR][1000 genomes]
rs1564557	1.00[CEU][hapmap];0.91[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs1586022	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1600829	0.97[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1600831	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs17238859	0.82[EUR][1000 genomes]
rs17238880	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs17819592	0.94[EUR][1000 genomes]
rs1834199	0.94[EUR][1000 genomes]
rs2052641	0.94[EUR][1000 genomes]
rs2161935	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs2170461	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2170462	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2459565	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2676181	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2733231	0.94[EUR][1000 genomes]
rs2899599	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs35813867	0.88[EUR][1000 genomes]
rs4287503	0.94[EUR][1000 genomes]
rs4594195	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4774869	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4774885	1.00[CEU][hapmap];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs480701	1.00[CEU][hapmap];0.94[EUR][1000 genomes]
rs6493888	0.94[EUR][1000 genomes]
rs7176472	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs7177197	0.82[EUR][1000 genomes]
rs74015901	0.88[EUR][1000 genomes]
rs8029710	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1545	chr15:56659498-56897381	Active TSS Strong transcription Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv471330	chr15:56659709-56896385	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv471506	chr15:56659709-56896385	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv498847	chr15:56667038-56896395	Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	esv2525559	chr15:56669294-56897412	Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv433294	chr15:56676457-56853535	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	esv3693203	chr15:56676457-56894478	Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
8	esv35150	chr15:56677730-56896304	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
9	nsv1049240	chr15:56820899-56890478	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:56850400-56853600	Weak transcription	Fetal Thymus	thymus

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