Variant report

Variant	rs12247717
Chromosome Location	chr10:59073568-59073569
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs11005759	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11005784	1.00[EUR][1000 genomes]
rs11005786	1.00[EUR][1000 genomes]
rs12243306	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12244976	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12247207	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12248875	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12249980	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12252204	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12252413	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12253016	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12254330	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12255219	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73295449	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv895543	chr10:58938552-59210800	Active TSS Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	2 gene(s)	inside rSNPs	diseases
2	nsv895544	chr10:58938552-59282980	Weak transcription Active TSS Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	3 gene(s)	inside rSNPs	diseases
3	nsv895545	chr10:58938552-59313872	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	3 gene(s)	inside rSNPs	diseases
4	nsv916857	chr10:58960110-59272160	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	3 gene(s)	inside rSNPs	diseases
5	nsv1038755	chr10:59071887-59161413	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:59073000-59074000	Enhancers	Brain Hippocampus Middle	brain
2	chr10:59073000-59075400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr10:59073400-59073800	Enhancers	Brain Cingulate Gyrus	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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