Variant report

Variant	rs74124062
Chromosome Location	chr10:25819052-25819053
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs16926075	1.00[AMR][1000 genomes]
rs16926077	1.00[AMR][1000 genomes]
rs16926082	1.00[AMR][1000 genomes]
rs1981118	1.00[AMR][1000 genomes]
rs57222731	1.00[AMR][1000 genomes]
rs57418758	1.00[AMR][1000 genomes]
rs58303369	1.00[AMR][1000 genomes]
rs61333610	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74124054	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74124056	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74124058	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74124059	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74124063	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74124068	1.00[AMR][1000 genomes]
rs74126217	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	esv3349863	chr10:25614571-25946379	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 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	chr10:25812800-25824200	Weak transcription	Cortex derived primary cultured neurospheres	brain

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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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