Variant report

Variant	rs12072932
Chromosome Location	chr1:57987778-57987779
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10493226	1.00[AMR][1000 genomes]
rs10493227	1.00[AMR][1000 genomes]
rs10493229	1.00[AMR][1000 genomes]
rs11207048	1.00[AMR][1000 genomes]
rs11207049	1.00[AMR][1000 genomes]
rs11207050	1.00[AMR][1000 genomes]
rs11207051	1.00[AMR][1000 genomes]
rs11207053	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11207054	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11804717	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11805586	1.00[AMR][1000 genomes]
rs11810273	1.00[AMR][1000 genomes]
rs12063470	1.00[AMR][1000 genomes]
rs12065019	1.00[AMR][1000 genomes]
rs12067444	1.00[AMR][1000 genomes]
rs12067490	1.00[AMR][1000 genomes]
rs12073810	1.00[AMR][1000 genomes]
rs4310463	1.00[AMR][1000 genomes]
rs4348747	1.00[AMR][1000 genomes]
rs4526638	1.00[AMR][1000 genomes]
rs4529731	1.00[AMR][1000 genomes]
rs4553222	1.00[AMR][1000 genomes]
rs56721199	1.00[AMR][1000 genomes]
rs56873272	1.00[AMR][1000 genomes]
rs58873103	1.00[AMR][1000 genomes]
rs59078890	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6681889	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6694496	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6700225	1.00[AMR][1000 genomes]
rs947243	1.00[AMR][1000 genomes]
rs947244	1.00[AMR][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:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:57983800-57988400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr1:57987000-57989000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr1:57987600-57989200	Enhancers	Hela-S3	cervix

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