Variant report

Variant	rs61495699
Chromosome Location	chr8:94960471-94960472
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs11990284	0.87[AFR][1000 genomes]
rs11990491	1.00[AMR][1000 genomes]
rs11997800	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59075005	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59138229	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73692985	0.87[AFR][1000 genomes]
rs73692989	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73692990	0.95[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	esv2754970	chr8:94675324-94991724	Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	48 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	chr8:94958000-94960600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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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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