Variant report

Variant	rs9696872
Chromosome Location	chr9:93741233-93741234
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 1 )

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

rs_ID	r²[population]
rs10761104	0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10820821	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10820822	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10991725	0.85[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs10991728	0.85[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs1155522	0.95[CHB][hapmap];0.83[JPT][hapmap];0.88[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs6479319	0.90[AMR][1000 genomes];0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7027577	0.81[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7873505	0.88[AMR][1000 genomes];0.89[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	nsv1046989	chr9:93353987-93800416	Transcr. at gene 5' and 3' Weak transcription Active TSS Strong transcription Enhancers Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	nsv893568	chr9:93539879-93774385	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs9696872	NOL8	cis	parietal	SCAN

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:93730400-93741600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr9:93737600-93741400	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr9:93738000-93741400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr9:93740400-93746200	Weak transcription	Dnd41	blood
5	chr9:93740800-93743200	Enhancers	HMEC	breast
6	chr9:93741000-93741800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr9:93741000-93742000	Enhancers	NHEK	skin
8	chr9:93741000-93742200	Enhancers	Pancreas	Pancrea
9	chr9:93741000-93742400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr9:93741000-93742600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr9:93741200-93741600	Active TSS	Rectal Mucosa Donor 29	rectum
12	chr9:93741200-93742000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr9:93741200-93742000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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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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