Variant report

Variant	rs2184255
Chromosome Location	chr9:96176203-96176204
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs10761237	0.80[ASW][hapmap]
rs10992723	0.91[EUR][1000 genomes]
rs10992728	0.89[EUR][1000 genomes]
rs11789176	0.85[CHB][hapmap];0.86[JPT][hapmap]
rs2841680	0.89[CHD][hapmap]
rs3901421	0.90[JPT][hapmap];0.85[YRI][hapmap];0.81[AFR][1000 genomes]
rs3933795	0.94[ASW][hapmap];0.85[CHD][hapmap];0.90[JPT][hapmap];0.95[LWK][hapmap];0.97[MKK][hapmap];0.89[YRI][hapmap];0.91[AFR][1000 genomes]
rs4310267	0.80[AFR][1000 genomes]
rs4563950	1.00[CEU][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs7020852	1.00[ASW][hapmap];1.00[CEU][hapmap];0.88[CHD][hapmap];0.95[GIH][hapmap];0.98[LWK][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];0.96[YRI][hapmap];0.97[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs7040832	0.83[AFR][1000 genomes]
rs72743489	0.90[EUR][1000 genomes]

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs2184255	ANKRD19	cis	cerebellum	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:96175800-96176800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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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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