Variant report

Variant	rs59700255
Chromosome Location	chr7:103672726-103672727
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs12536622	0.86[EUR][1000 genomes]
rs12539921	0.86[EUR][1000 genomes]
rs17158452	0.86[EUR][1000 genomes]
rs17158464	0.86[EUR][1000 genomes]
rs4729954	0.86[EUR][1000 genomes]
rs4729955	0.86[EUR][1000 genomes]
rs4729956	0.86[EUR][1000 genomes]
rs55695552	0.83[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs56022599	0.86[EUR][1000 genomes]
rs66797006	0.86[EUR][1000 genomes]
rs67580058	0.86[EUR][1000 genomes]
rs73185501	0.90[EUR][1000 genomes]
rs73187416	0.86[EUR][1000 genomes]
rs73189312	0.81[EUR][1000 genomes]
rs7798617	0.82[AMR][1000 genomes];0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv888924	chr7:103637906-103706936	Enhancers Active TSS Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1018253	chr7:103669491-103731850	Enhancers Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	Chromatin interactive region lncRNA	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	chr7:103672000-103673600	Enhancers	K562	blood

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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