Variant report

Variant	rs9372372
Chromosome Location	chr6:114020783-114020784
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 3 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs2588026	0.81[EUR][1000 genomes]
rs4142803	0.86[JPT][hapmap];0.87[YRI][hapmap]
rs773685	0.82[EUR][1000 genomes]

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs9372372	FLJ34503	cis	cerebellum	SCAN
rs9372372	GOPC	cis	parietal	SCAN
rs9372372	WASF1	cis	cerebellum	SCAN

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:114015800-114023000	Weak transcription	Rectal Mucosa Donor 31	rectum
2	chr6:114016200-114023000	Weak transcription	Fetal Lung	lung
3	chr6:114016400-114022000	Weak transcription	Stomach Mucosa	stomach
4	chr6:114018800-114020800	Enhancers	HSMMtube	muscle
5	chr6:114020000-114021200	Enhancers	HepG2	liver

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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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