Variant report

Variant	rs9857367
Chromosome Location	chr3:118571065-118571066
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs28392691	1.00[AMR][1000 genomes]
rs58420381	1.00[AMR][1000 genomes]
rs6768020	1.00[AMR][1000 genomes]
rs6796798	1.00[AMR][1000 genomes]
rs72966899	1.00[AMR][1000 genomes]
rs72968606	1.00[AMR][1000 genomes]
rs72968612	1.00[AMR][1000 genomes]
rs72968632	1.00[AMR][1000 genomes]
rs72968654	1.00[AMR][1000 genomes]
rs72970438	1.00[AMR][1000 genomes]
rs72970470	1.00[AMR][1000 genomes]
rs72970472	1.00[AMR][1000 genomes]
rs7623832	1.00[AMR][1000 genomes]
rs7624134	1.00[AMR][1000 genomes]
rs7625109	1.00[AMR][1000 genomes]
rs9289118	1.00[AMR][1000 genomes]
rs9814712	1.00[AMR][1000 genomes]
rs9826100	1.00[AMR][1000 genomes]
rs9827711	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9835052	1.00[AMR][1000 genomes]
rs9836742	0.92[YRI][hapmap]
rs9840552	1.00[AMR][1000 genomes]
rs9841148	1.00[AMR][1000 genomes]
rs9847137	1.00[AMR][1000 genomes]
rs9848498	1.00[AMR][1000 genomes]
rs9854365	1.00[AMR][1000 genomes]
rs9859319	1.00[AMR][1000 genomes]
rs9860173	1.00[YRI][hapmap]
rs9862313	1.00[AMR][1000 genomes]
rs9862556	1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs9876041	1.00[AMR][1000 genomes]
rs9882006	1.00[YRI][hapmap];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv963353	chr3:118554595-118572118	Active TSS ZNF genes & repeats Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
2	esv3487859	chr3:118570588-119419623	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
3	esv3487860	chr3:118570588-119419623	Strong transcription Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:118570000-118571200	ZNF genes & repeats	GM12878-XiMat	blood
2	chr3:118570200-118571200	Active TSS	Duodenum Mucosa	Duodenum
3	chr3:118570400-118571200	Active TSS	Primary T cells fromperipheralblood	blood
4	chr3:118570400-118571200	Enhancers	Dnd41	blood
5	chr3:118570400-118571200	Active TSS	Hela-S3	cervix
6	chr3:118570400-118571200	Active TSS	HepG2	liver
7	chr3:118570600-118571200	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
8	chr3:118570600-118571400	Active TSS	A549	lung
9	chr3:118570600-118571400	Active TSS	K562	blood
10	chr3:118570800-118571200	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
11	chr3:118570800-118571200	Active TSS	Primary Natural Killer cells fromperipheralblood	blood

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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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