Variant report

Variant	rs944990
Chromosome Location	chr9:96191004-96191005
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10761229	0.89[GIH][hapmap]
rs10821123	0.92[ASW][hapmap];0.88[CHD][hapmap];0.89[JPT][hapmap];0.90[LWK][hapmap];0.95[MKK][hapmap];0.91[YRI][hapmap];0.89[AFR][1000 genomes]
rs10821125	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10821128	0.89[GIH][hapmap]
rs10992716	0.82[ASW][hapmap];0.82[YRI][hapmap]
rs10992733	0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10992744	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10992749	0.89[GIH][hapmap]
rs10992769	0.85[CEU][hapmap];0.86[CHB][hapmap];0.94[JPT][hapmap];0.93[AMR][1000 genomes];0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11791374	0.89[GIH][hapmap]
rs12379660	0.83[CHB][hapmap];0.80[CHD][hapmap];0.89[GIH][hapmap]
rs2100928	0.82[YRI][hapmap]
rs4743922	0.89[GIH][hapmap]
rs4743923	0.83[GIH][hapmap]
rs5019496	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7864396	0.83[GIH][hapmap]

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:96185800-96208200	Weak transcription	Gastric	stomach
2	chr9:96186000-96208200	Weak transcription	Pancreas	Pancrea
3	chr9:96186600-96208200	Weak transcription	Lung	lung
4	chr9:96190600-96192800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr9:96190600-96196600	Weak transcription	Placenta	Placenta
6	chr9:96190800-96193200	Weak transcription	Fetal Intestine Large	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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