Variant report

Variant	rs12723203
Chromosome Location	chr15:26396982-26396983
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs11117818	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12027079	0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12030946	0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12032192	0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12044340	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4332417	0.94[ASN][1000 genomes]
rs4504960	0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4846822	0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4846825	0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs71643451	0.82[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs72745316	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7516676	0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7534753	0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7535701	0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7543133	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7543660	0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7547261	0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7554040	0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv34047	chr15:26251847-26421585	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv832938	chr15:26322087-26501451	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv568598	chr15:26327466-26821125	Enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
4	nsv832939	chr15:26386767-26477263	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
5	nsv522418	chr15:26393202-26402601	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	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	chr15:26393200-26400600	Weak transcription	Brain Germinal Matrix	brain

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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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