Variant report

Variant	rs56833280
Chromosome Location	chr9:96121967-96121968
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs10992715	0.84[AFR][1000 genomes];0.96[AMR][1000 genomes];0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12002078	0.83[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs12004484	0.83[AMR][1000 genomes]
rs13293140	0.93[AMR][1000 genomes];0.80[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs16909074	0.80[AMR][1000 genomes]
rs34360996	0.83[AMR][1000 genomes]
rs34590502	0.80[AMR][1000 genomes]
rs35807838	0.83[AMR][1000 genomes]
rs58361139	0.86[AMR][1000 genomes]
rs62572859	0.80[AMR][1000 genomes]
rs7850794	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv893576	chr9:95789960-96158277	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
2	esv2761278	chr9:96115678-96126104	ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3' Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:96109200-96127800	Weak transcription	Right Atrium	heart
2	chr9:96111200-96122400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr9:96120200-96125600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr9:96120600-96123200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
5	chr9:96121000-96125000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
6	chr9:96121200-96122000	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
7	chr9:96121200-96126200	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
8	chr9:96121400-96124800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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