Variant report

Variant	rs2691455
Chromosome Location	chr1:57991233-57991234
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 60 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:54)

rs_ID	r²[population]
rs10493229	1.00[EUR][1000 genomes]
rs10889057	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11207053	1.00[EUR][1000 genomes]
rs11803909	1.00[EUR][1000 genomes]
rs11805586	1.00[EUR][1000 genomes]
rs11810273	1.00[EUR][1000 genomes]
rs12067444	1.00[EUR][1000 genomes]
rs12067490	1.00[EUR][1000 genomes]
rs1341311	1.00[EUR][1000 genomes]
rs1341312	1.00[GIH][hapmap]
rs1404389	1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs1417761	1.00[GIH][hapmap];1.00[AMR][1000 genomes]
rs1524706	1.00[EUR][1000 genomes]
rs1524710	1.00[AMR][1000 genomes]
rs1524712	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1524718	1.00[GIH][hapmap]
rs1524722	0.82[YRI][hapmap]
rs1524731	1.00[EUR][1000 genomes]
rs1534048	1.00[EUR][1000 genomes]
rs17115844	1.00[GIH][hapmap]
rs1815685	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1880442	0.82[YRI][hapmap];1.00[EUR][1000 genomes]
rs1935045	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2204376	1.00[EUR][1000 genomes]
rs2265623	1.00[EUR][1000 genomes]
rs2691443	1.00[EUR][1000 genomes]
rs2691444	1.00[GIH][hapmap];0.82[LWK][hapmap];1.00[EUR][1000 genomes]
rs2691445	1.00[GIH][hapmap];1.00[EUR][1000 genomes]
rs2691447	1.00[GIH][hapmap];1.00[EUR][1000 genomes]
rs2691448	1.00[EUR][1000 genomes]
rs2793624	1.00[GIH][hapmap]
rs2793641	1.00[GIH][hapmap];1.00[EUR][1000 genomes]
rs2805850	1.00[GIH][hapmap];1.00[EUR][1000 genomes]
rs2805851	1.00[EUR][1000 genomes]
rs28391765	1.00[EUR][1000 genomes]
rs28621926	1.00[EUR][1000 genomes]
rs4310463	1.00[EUR][1000 genomes]
rs4348747	1.00[EUR][1000 genomes]
rs4526638	1.00[EUR][1000 genomes]
rs4529731	1.00[EUR][1000 genomes]
rs4553222	1.00[EUR][1000 genomes]
rs4554738	1.00[EUR][1000 genomes]
rs486804	1.00[GIH][hapmap]
rs523282	1.00[GIH][hapmap]
rs539257	1.00[GIH][hapmap]
rs56873272	1.00[EUR][1000 genomes]
rs58873103	1.00[EUR][1000 genomes]
rs60116819	1.00[EUR][1000 genomes]
rs60867983	0.82[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs72908597	1.00[EUR][1000 genomes]
rs7551052	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs947237	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs947238	1.00[EUR][1000 genomes]
rs947241	1.00[GIH][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv817216	chr1:57801783-58130775	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1001771	chr1:57837089-58068175	Bivalent/Poised TSS Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv870908	chr1:57884310-58037783	Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv1012555	chr1:57950355-58103389	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv870802	chr1:57965114-58037031	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv1015057	chr1:57976993-58793962	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:57988600-58001400	Weak transcription	Stomach Mucosa	stomach
2	chr1:57989200-58012200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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