Variant report

Variant	rs7823118
Chromosome Location	chr8:63495898-63495899
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10090181	1.00[AMR][1000 genomes]
rs10092099	1.00[AMR][1000 genomes]
rs10092296	1.00[AMR][1000 genomes]
rs10092935	1.00[AMR][1000 genomes]
rs10094032	1.00[AMR][1000 genomes]
rs10095868	1.00[AMR][1000 genomes]
rs10096226	1.00[AMR][1000 genomes]
rs10100399	1.00[AMR][1000 genomes]
rs10101425	1.00[AMR][1000 genomes]
rs10101617	1.00[AMR][1000 genomes]
rs10104556	1.00[AMR][1000 genomes]
rs10957230	1.00[AMR][1000 genomes]
rs13438922	1.00[AMR][1000 genomes]
rs13439208	1.00[AMR][1000 genomes]
rs13439470	1.00[AMR][1000 genomes]
rs16928916	1.00[AMR][1000 genomes]
rs28392810	1.00[AMR][1000 genomes]
rs28407937	1.00[AMR][1000 genomes]
rs28451590	1.00[AMR][1000 genomes]
rs28570147	1.00[AMR][1000 genomes]
rs28639415	1.00[AMR][1000 genomes]
rs28645735	1.00[AMR][1000 genomes]
rs28666681	1.00[AMR][1000 genomes]
rs28713340	1.00[AMR][1000 genomes]
rs28714560	1.00[AMR][1000 genomes]
rs28728121	1.00[AMR][1000 genomes]
rs28735390	1.00[AMR][1000 genomes]
rs6472041	1.00[AMR][1000 genomes]
rs6988031	1.00[AMR][1000 genomes]
rs6992264	1.00[AMR][1000 genomes]
rs7821718	1.00[AMR][1000 genomes]
rs7837461	1.00[AMR][1000 genomes]
rs9657077	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	nsv1018879	chr8:63281724-63937632	Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv831339	chr8:63312449-63501127	Enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv890959	chr8:63449156-63515522	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:63490600-63497000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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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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