Variant report

Variant	rs58628492
Chromosome Location	chr7:86272096-86272097
allele	A/C
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:16)

rs_ID	r²[population]
rs55906351	0.81[AFR][1000 genomes]
rs56699849	0.93[AFR][1000 genomes]
rs61383608	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61398217	1.00[AMR][1000 genomes]
rs73396494	1.00[AMR][1000 genomes]
rs73398435	1.00[AMR][1000 genomes]
rs73704920	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73704924	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73704926	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73704938	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73704951	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73704953	1.00[AMR][1000 genomes]
rs73704959	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73704960	0.81[AFR][1000 genomes]
rs73704986	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73704987	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1025032	chr7:86032479-86642973	Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv831053	chr7:86268171-86440999	Bivalent Enhancer Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:86267000-86272600	Weak transcription	Brain Inferior Temporal Lobe	brain
2	chr7:86269600-86272800	Weak transcription	Brain Substantia Nigra	brain
3	chr7:86270000-86272600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
4	chr7:86271800-86272400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr7:86271800-86272400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr7:86271800-86272400	Enhancers	Brain Cingulate Gyrus	brain
7	chr7:86272000-86272600	Weak transcription	Brain Angular Gyrus	brain
8	chr7:86272000-86272600	Weak transcription	Brain Anterior Caudate	brain

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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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