Variant report

Variant	rs9387476
Chromosome Location	chr6:117774775-117774776
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10434878	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11153658	1.00[CEU][hapmap];1.00[JPT][hapmap];0.85[YRI][hapmap];1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12176352	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1998206	1.00[JPT][hapmap]
rs28639589	0.85[YRI][hapmap];0.82[AFR][1000 genomes]
rs3777973	0.94[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs4946252	1.00[JPT][hapmap];0.97[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4946255	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9320599	1.00[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.87[YRI][hapmap];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9374656	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9374657	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9385009	0.97[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs9385011	1.00[JPT][hapmap]
rs9387471	0.85[YRI][hapmap]
rs9401002	0.87[YRI][hapmap];0.82[AFR][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	nsv532050	chr6:117528154-118203005	ZNF genes & repeats Enhancers Bivalent Enhancer Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
2	nsv521325	chr6:117772143-117776185	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:117769600-117779400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr6:117770000-117778000	Weak transcription	Rectal Mucosa Donor 29	rectum
3	chr6:117772600-117775400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr6:117772800-117778000	Weak transcription	Rectal Mucosa Donor 31	rectum
5	chr6:117773000-117778400	Weak transcription	Stomach Mucosa	stomach
6	chr6:117773200-117777000	Weak transcription	Duodenum Mucosa	Duodenum
7	chr6:117773600-117777000	Weak transcription	Fetal Intestine Large	intestine
8	chr6:117773600-117777200	Weak transcription	A549	lung
9	chr6:117773600-117777600	Weak transcription	HepG2	liver
10	chr6:117773600-117778000	Weak transcription	Fetal Intestine Small	intestine

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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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