Variant report

Variant	rs61061024
Chromosome Location	chr2:73357640-73357641
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs13404068	0.86[EUR][1000 genomes]
rs2421099	0.86[EUR][1000 genomes]
rs56931614	0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs56992198	0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs58617186	0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs58649746	0.88[ASN][1000 genomes]
rs58659495	0.88[EUR][1000 genomes]
rs59108557	0.85[EUR][1000 genomes]
rs59802755	0.88[EUR][1000 genomes]
rs60341789	0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs61652727	0.85[EUR][1000 genomes]
rs62147756	0.84[EUR][1000 genomes]
rs67421457	0.85[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1006801	chr2:73305056-73431711	Weak transcription Active TSS Genic enhancers Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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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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