Variant report

Variant	rs62461683
Chromosome Location	chr7:79600671-79600672
allele	A/G
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]
rs10237226	0.99[ASN][1000 genomes]
rs10259572	0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11983179	0.86[EUR][1000 genomes]
rs12666674	0.97[ASN][1000 genomes]
rs12667856	0.99[ASN][1000 genomes]
rs12670640	0.97[ASN][1000 genomes]
rs12670674	0.97[ASN][1000 genomes]
rs17153199	0.97[ASN][1000 genomes]
rs4574785	0.97[ASN][1000 genomes]
rs56016880	0.86[EUR][1000 genomes]
rs56150062	0.86[EUR][1000 genomes]
rs56191620	0.97[ASN][1000 genomes]
rs62461684	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6466880	0.86[EUR][1000 genomes]
rs6466884	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6946783	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs763822	0.86[EUR][1000 genomes]
rs7811115	0.86[EUR][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	nsv888522	chr7:79402551-79619012	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv1032480	chr7:79558011-79625086	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv429785	chr7:79589749-80177049	Bivalent/Poised TSS Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:1 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:79599600-79600800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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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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