Variant report

Variant	rs12918232
Chromosome Location	chr16:48690695-48690696
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs2047601	0.91[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs2354580	0.93[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs3785138	0.91[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs3826176	0.91[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs4028695	0.80[AMR][1000 genomes]
rs4315324	0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6500392	0.90[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs6500393	0.91[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs8046716	0.89[AMR][1000 genomes]
rs8057605	0.90[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs9930255	0.84[AMR][1000 genomes];0.80[EUR][1000 genomes]

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs12918232	N4BP1	cis	multi-tissue	Pritchard

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:48690400-48690800	Active TSS	Spleen	Spleen

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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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