Variant report

Variant	rs2307
Chromosome Location	chr4:31074822-31074823
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs28571043	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs34623229	0.81[EUR][1000 genomes]
rs55707833	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56393119	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs59848134	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6836890	0.82[EUR][1000 genomes]
rs6847526	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs73812504	0.94[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs73812506	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs73812507	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs73812508	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs73812512	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73812515	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73812516	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73815167	0.94[AMR][1000 genomes];0.92[EUR][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	nsv998450	chr4:30823631-31628179	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
2	nsv289500	chr4:31069939-31076406	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
3	nsv1007884	chr4:31071934-31680623	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:31058000-31077200	Weak transcription	Aorta	Aorta
2	chr4:31066400-31088600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr4:31070600-31088400	Weak transcription	Fetal Stomach	stomach
4	chr4:31071000-31077000	Weak transcription	Fetal Muscle Leg	muscle
5	chr4:31072800-31075000	Weak transcription	Fetal Lung	lung
6	chr4:31073400-31075600	Enhancers	Pancreatic Islets	Pancreatic Islet
7	chr4:31074600-31076000	Weak transcription	Fetal Heart	heart

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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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