Variant report

Variant	rs7923167
Chromosome Location	chr10:53706338-53706339
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10508952	0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11592770	0.88[EUR][1000 genomes]
rs11592820	0.88[EUR][1000 genomes]
rs11593309	0.84[EUR][1000 genomes]
rs11594267	0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11596469	0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11596918	0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12245187	0.87[EUR][1000 genomes]
rs12255275	0.93[ASN][1000 genomes]
rs16925100	0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs16925106	0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs16925131	0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs16925132	0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs57940938	0.87[ASN][1000 genomes]
rs7088540	0.81[EUR][1000 genomes]
rs7895143	0.92[ASN][1000 genomes]
rs7902101	0.94[ASN][1000 genomes]
rs7905683	0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1045692	chr10:53301450-54086823	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
2	esv3315052	chr10:53699381-53707128	Weak transcription	n/a	n/a	inside rSNPs	diseases
3	esv3315063	chr10:53699381-53707128	Weak transcription	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	chr10:53706000-53710200	Weak transcription	Right Atrium	heart

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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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