Variant report

Variant	rs73487737
Chromosome Location	chr11:58283538-58283539
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 24 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs58433279	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58454093	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59856964	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73470711	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73470713	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73470722	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73470723	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73470726	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73470731	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73470732	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73470748	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73470749	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73470751	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73470756	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73470758	0.85[AMR][1000 genomes]
rs73472048	0.83[AMR][1000 genomes]
rs73485922	0.85[AMR][1000 genomes]
rs73485926	0.85[AMR][1000 genomes]
rs73485934	0.85[AMR][1000 genomes]
rs73485945	1.00[AMR][1000 genomes]
rs73487714	1.00[AMR][1000 genomes]
rs73487735	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73487770	1.00[AFR][1000 genomes];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	nsv1054205	chr11:57544264-58358509	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 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	chr11:58281800-58291400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr11:58281800-58291800	Weak transcription	Muscle Satellite Cultured Cells	--

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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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