Variant report

Variant	rs61601218
Chromosome Location	chr8:96287083-96287084
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs60219110	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73266468	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73266470	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73266472	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73266479	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73266483	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73268333	1.00[AFR][1000 genomes];1.00[AMR][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	nsv1023866	chr8:96273255-96306378	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 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	chr8:96286000-96287200	Enhancers	Fetal Heart	heart

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

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