Variant report

Variant	rs72951825
Chromosome Location	chr1:86876391-86876392
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs11161796	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11161797	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11801454	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11803763	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11804733	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11810074	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12079988	1.00[AMR][1000 genomes]
rs12096446	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs34372019	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56841249	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72949810	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72949857	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72949858	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72949874	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72949875	1.00[AFR][1000 genomes]
rs72949879	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72949884	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72949902	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72951830	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72951832	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72951845	0.90[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv546722	chr1:86278315-86891073	Enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	9 gene(s)	inside rSNPs	diseases
2	nsv1003838	chr1:86591841-87212231	Flanking Bivalent TSS/Enh Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
3	nsv1002541	chr1:86689088-86905902	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	3 gene(s)	inside rSNPs	diseases
4	nsv871081	chr1:86806372-86892819	Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	3 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	chr1:86862400-86876400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr1:86873400-86876600	Weak transcription	Right Atrium	heart
3	chr1:86875200-86876400	Active TSS	Spleen	Spleen

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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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