Variant report

Variant	rs7474799
Chromosome Location	chr10:95598671-95598672
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs10882349	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs10882350	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10882351	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10882352	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs10882353	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs10882354	0.80[EUR][1000 genomes]
rs1820362	0.87[AFR][1000 genomes];0.90[AMR][1000 genomes];0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2901715	0.80[AMR][1000 genomes]
rs7899974	0.84[AMR][1000 genomes];0.82[EUR][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	esv13320	chr10:95594800-95609228	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:95594800-95599800	Enhancers	Fetal Intestine Large	intestine
2	chr10:95595200-95599800	Enhancers	Fetal Intestine Small	intestine
3	chr10:95597400-95599600	Enhancers	Duodenum Mucosa	Duodenum
4	chr10:95598000-95600800	Weak transcription	Cortex derived primary cultured neurospheres	brain
5	chr10:95598400-95601800	Weak transcription	Small Intestine	intestine

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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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