Variant report

Variant	rs9297941
Chromosome Location	chr8:87658739-87658740
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs10094222	0.82[CEU][hapmap];0.95[GIH][hapmap];0.91[JPT][hapmap];0.89[MEX][hapmap];0.91[TSI][hapmap]
rs1009574	0.88[CEU][hapmap];0.87[JPT][hapmap];0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10106841	0.82[CEU][hapmap];0.81[CHB][hapmap];0.82[JPT][hapmap]
rs10216710	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10216953	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs13258590	0.85[CEU][hapmap];0.90[CHB][hapmap];0.93[CHD][hapmap];0.91[JPT][hapmap];0.83[ASN][1000 genomes]
rs13268738	0.85[CHB][hapmap];0.93[CHD][hapmap];0.95[JPT][hapmap];0.92[ASN][1000 genomes]
rs1441243	0.85[CEU][hapmap];0.90[CHB][hapmap];0.93[CHD][hapmap];0.95[GIH][hapmap];0.95[JPT][hapmap];0.95[TSI][hapmap]
rs16916427	0.96[CEU][hapmap];1.00[CHB][hapmap];0.93[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap]
rs3735967	0.85[CEU][hapmap];0.95[GIH][hapmap];0.87[JPT][hapmap];0.87[TSI][hapmap]
rs3779790	0.81[CEU][hapmap];0.80[CHB][hapmap];0.86[CHD][hapmap];0.95[GIH][hapmap];0.95[JPT][hapmap];0.87[TSI][hapmap];0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs3779801	0.92[CEU][hapmap];0.81[CHB][hapmap];0.81[JPT][hapmap]
rs59109039	0.95[EUR][1000 genomes];0.85[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	nsv1023510	chr8:87429001-87874948	Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
2	nsv818641	chr8:87643741-87658739	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs9297941	RBM24	trans	parietal	SCAN
rs9297941	RIPK2	cis	parietal	SCAN

Chromatin state (count:0 , 50 per page) page:

No data

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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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