Variant report

Variant	rs58914587
Chromosome Location	chr1:119192159-119192160
allele	A/C
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:17)

rs_ID	r²[population]
rs57286151	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57700973	1.00[AMR][1000 genomes]
rs57767525	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58060170	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58275617	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58936827	1.00[AMR][1000 genomes]
rs61064384	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73005255	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73005256	1.00[AMR][1000 genomes]
rs73005263	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73005283	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73016762	1.00[AMR][1000 genomes]
rs73016774	1.00[AMR][1000 genomes]
rs73020856	1.00[AMR][1000 genomes]
rs74114507	1.00[AMR][1000 genomes]
rs74116009	1.00[AMR][1000 genomes]
rs7543504	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3494191	chr1:118772550-119719548	Enhancers Strong transcription Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
2	esv3494192	chr1:118772550-119719548	Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Enhancers Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:119190800-119194200	Enhancers	Fetal Heart	heart
2	chr1:119191800-119193600	Enhancers	Colon Smooth Muscle	Colon
3	chr1:119192000-119192400	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr1:119192000-119192400	Enhancers	Fetal Muscle Leg	muscle
5	chr1:119192000-119192600	Enhancers	Skeletal Muscle Female	skeletal muscle
6	chr1:119192000-119194200	Enhancers	Skeletal Muscle Male	skeletal muscle

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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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