Variant report

Variant	rs60319911
Chromosome Location	chr14:79958735-79958736
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs11847465	1.00[AMR][1000 genomes]
rs11848738	1.00[AMR][1000 genomes]
rs11852085	1.00[AMR][1000 genomes]
rs55708063	1.00[AMR][1000 genomes]
rs57252489	1.00[AMR][1000 genomes]
rs57281369	1.00[AMR][1000 genomes]
rs57656995	1.00[AMR][1000 genomes]
rs58351352	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58357059	1.00[AMR][1000 genomes]
rs59078244	1.00[AMR][1000 genomes]
rs59472910	1.00[AMR][1000 genomes]
rs59809006	1.00[AMR][1000 genomes]
rs60502118	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60701970	0.90[AFR][1000 genomes]
rs60734338	1.00[AMR][1000 genomes]
rs61002775	1.00[AMR][1000 genomes]
rs61029849	1.00[AMR][1000 genomes]
rs61309702	1.00[AMR][1000 genomes]
rs72696784	1.00[AMR][1000 genomes]
rs74068005	1.00[AMR][1000 genomes]
rs74068052	1.00[AMR][1000 genomes]
rs74068054	1.00[AMR][1000 genomes]
rs74068066	1.00[AMR][1000 genomes]
rs74068069	1.00[AMR][1000 genomes]
rs74068072	1.00[AMR][1000 genomes]
rs74068091	1.00[AMR][1000 genomes]
rs74068696	1.00[AMR][1000 genomes]
rs74068698	0.89[AFR][1000 genomes]
rs74070211	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74070212	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74070239	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74070242	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74070257	1.00[AMR][1000 genomes]
rs74070258	1.00[AMR][1000 genomes]
rs74070263	1.00[AMR][1000 genomes]
rs74070265	1.00[AMR][1000 genomes]
rs74070266	1.00[AMR][1000 genomes]
rs74070271	1.00[AMR][1000 genomes]
rs74070273	1.00[AMR][1000 genomes]
rs74070276	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv902110	chr14:79624492-79998294	Bivalent/Poised TSS Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv1045241	chr14:79885361-80734201	Weak transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
3	nsv1039622	chr14:79908702-80266601	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv902112	chr14:79939393-80050771	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS	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	chr14:79958000-79959600	Weak transcription	Placenta Amnion	Placenta Amnion

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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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