Variant report

Variant	rs12082164
Chromosome Location	chr1:84292000-84292001
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 1 )

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

rs_ID	r²[population]
rs1010435	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs11163846	0.86[EUR][1000 genomes]
rs11163852	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1159534	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12071675	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12083999	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs3850438	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4628522	0.92[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7531463	0.86[EUR][1000 genomes]

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs12082164	BXDC5,RPF1	cis	hippocampus	BrainEAC

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:84281400-84316600	Weak transcription	Pancreas	Pancrea
2	chr1:84281600-84293000	Weak transcription	Fetal Heart	heart
3	chr1:84285800-84305000	Weak transcription	Liver	Liver
4	chr1:84286600-84293400	Weak transcription	Placenta	Placenta
5	chr1:84290200-84294200	Weak transcription	Pancreatic Islets	Pancreatic Islet

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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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