Variant report

Variant	rs73492018
Chromosome Location	chr11:62766234-62766235
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs1004836	0.85[AMR][1000 genomes]
rs11231283	0.85[AMR][1000 genomes]
rs11231291	0.85[AMR][1000 genomes]
rs11231292	0.85[AMR][1000 genomes]
rs11231293	0.85[AMR][1000 genomes]
rs11231298	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11820657	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11828074	0.85[AMR][1000 genomes]
rs11828160	0.85[AMR][1000 genomes]
rs12276943	0.85[AMR][1000 genomes]
rs12281345	0.93[AFR][1000 genomes]
rs12293329	0.85[AMR][1000 genomes]
rs12293966	0.85[AMR][1000 genomes]
rs12295679	0.85[AMR][1000 genomes]
rs57066277	0.85[AMR][1000 genomes]
rs57932955	0.85[AMR][1000 genomes]
rs58855055	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60359411	0.85[AMR][1000 genomes]
rs61380596	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61510834	0.85[AMR][1000 genomes]
rs67603137	0.85[AMR][1000 genomes]
rs7125335	0.85[AMR][1000 genomes]
rs7950683	0.85[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	nsv532283	chr11:62201358-62863475	Enhancers Flanking Active TSS Genic enhancers Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1433 gene(s)	inside rSNPs	diseases
2	nsv1041770	chr11:62610353-62871767	Enhancers Weak transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	263 gene(s)	inside rSNPs	diseases
3	esv34011	chr11:62652779-62993702	Weak transcription Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:62765800-62767400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
2	chr11:62766000-62767400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr11:62766200-62766800	Enhancers	iPS DF 6.9 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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