Variant report

Variant	rs12608386
Chromosome Location	chr18:24995664-24995665
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1105237	0.82[ASN][1000 genomes]
rs11083215	0.91[EUR][1000 genomes]
rs1519132	0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1607485	0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs16943627	0.91[EUR][1000 genomes]
rs28855421	0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs35021089	0.86[EUR][1000 genomes]
rs7228825	0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7244333	0.90[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3331699	chr18:24864438-25095929	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	esv2761996	chr18:24866083-25818618	Flanking Active TSS Enhancers Strong transcription Weak transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
3	nsv833601	chr18:24908240-25080975	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv833602	chr18:24993030-25180823	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:24993600-24995800	Enhancers	Fetal Kidney	kidney
2	chr18:24993800-24996000	Enhancers	Fetal Intestine Small	intestine
3	chr18:24994600-24996000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr18:24994600-24996800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr18:24994800-25000000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr18:24995000-24999800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr18:24995000-24999800	Weak transcription	Fetal Muscle Leg	muscle
8	chr18:24995200-24996400	Enhancers	HepG2	liver
9	chr18:24995600-24995800	Enhancers	Psoas Muscle	Psoas

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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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