Variant report

Variant	rs4631527
Chromosome Location	chr9:110270036-110270037
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs10759240	0.86[CHB][hapmap]
rs10816521	0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13302327	0.90[ASN][1000 genomes]
rs2051001	0.95[ASN][1000 genomes]
rs58843994	0.82[EUR][1000 genomes]
rs62570074	0.81[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	nsv530948	chr9:109760752-110413602	Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	57 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:110267000-110270200	Weak transcription	Aorta	Aorta
2	chr9:110267600-110270800	Weak transcription	Duodenum Mucosa	Duodenum
3	chr9:110267600-110270800	Weak transcription	Stomach Mucosa	stomach
4	chr9:110267800-110270600	Weak transcription	NHLF	lung
5	chr9:110267800-110272200	Weak transcription	Rectal Mucosa Donor 31	rectum
6	chr9:110269600-110272200	Weak transcription	Spleen	Spleen

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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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