Variant report

Variant	rs73275568
Chromosome Location	chr14:69490649-69490650
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs17106764	1.00[AMR][1000 genomes]
rs17106793	1.00[AMR][1000 genomes]
rs56922727	1.00[AMR][1000 genomes]
rs57103818	1.00[AMR][1000 genomes]
rs58395904	1.00[AMR][1000 genomes]
rs59157439	1.00[AMR][1000 genomes]
rs59871527	1.00[AMR][1000 genomes]
rs60643493	1.00[AMR][1000 genomes]
rs60660183	1.00[AMR][1000 genomes]
rs7142735	1.00[AMR][1000 genomes]
rs73275510	1.00[AMR][1000 genomes]
rs73275520	1.00[AMR][1000 genomes]
rs73275583	1.00[AMR][1000 genomes]
rs73275592	1.00[AMR][1000 genomes]
rs73275597	1.00[AMR][1000 genomes]
rs73275598	1.00[AMR][1000 genomes]
rs73275599	1.00[AMR][1000 genomes]
rs73275602	1.00[AMR][1000 genomes]
rs73277010	1.00[AMR][1000 genomes]
rs73277013	1.00[AMR][1000 genomes]
rs73277015	1.00[AMR][1000 genomes]
rs73277016	1.00[AMR][1000 genomes]
rs73277032	1.00[AMR][1000 genomes]
rs73278952	1.00[AMR][1000 genomes]
rs73278958	1.00[AMR][1000 genomes]
rs73278965	1.00[AMR][1000 genomes]
rs73278972	1.00[AMR][1000 genomes]
rs73278980	1.00[AMR][1000 genomes]
rs73278990	1.00[AMR][1000 genomes]
rs73278996	1.00[AMR][1000 genomes]
rs73280821	1.00[AMR][1000 genomes]
rs73280853	1.00[AMR][1000 genomes]
rs73280860	1.00[AMR][1000 genomes]
rs73280900	1.00[AMR][1000 genomes]
rs73282607	1.00[AMR][1000 genomes]
rs73282617	1.00[AMR][1000 genomes]
rs8016668	1.00[AMR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832823	chr14:69388853-69567638	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:69473000-69503600	Weak transcription	Right Atrium	heart
2	chr14:69486000-69503600	Weak transcription	iPS DF 19.11 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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