Variant report

Variant	rs12315482
Chromosome Location	chr12:46015462-46015463
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11183089	1.00[AMR][1000 genomes]
rs11183121	1.00[AMR][1000 genomes]
rs12302919	1.00[AMR][1000 genomes]
rs12305710	1.00[AMR][1000 genomes]
rs12309449	1.00[AMR][1000 genomes]
rs12321765	1.00[AMR][1000 genomes]
rs57162521	1.00[AMR][1000 genomes]
rs59594539	1.00[AMR][1000 genomes]
rs74081330	1.00[AMR][1000 genomes]
rs74081337	1.00[AMR][1000 genomes]
rs74081344	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74081888	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832395	chr12:45841765-46039297	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	esv2751099	chr12:45960118-46043633	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv983462	chr12:46008670-46015543	Weak transcription Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:46015000-46017600	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr12:46015400-46017000	Enhancers	Primary neutrophils fromperipheralblood	blood
3	chr12:46015400-46017000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood

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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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