Variant report

Variant	rs60799783
Chromosome Location	chr15:53398287-53398288
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs16965376	1.00[EUR][1000 genomes]
rs16965677	1.00[EUR][1000 genomes]
rs57717458	1.00[EUR][1000 genomes]
rs58972964	1.00[EUR][1000 genomes]
rs60615330	1.00[EUR][1000 genomes]
rs60841107	1.00[EUR][1000 genomes]
rs73402090	1.00[EUR][1000 genomes]
rs73403616	0.92[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73403621	0.92[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73403624	0.93[AFR][1000 genomes]
rs73403630	0.93[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73403632	0.85[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73403635	0.85[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73403645	0.85[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73403662	1.00[EUR][1000 genomes]
rs73403677	1.00[EUR][1000 genomes]
rs73403683	1.00[EUR][1000 genomes]
rs73403684	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv833007	chr15:53264564-53453525	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv904221	chr15:53279378-53434365	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	esv3343986	chr15:53284440-53571936	Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv1037630	chr15:53324645-53708925	Weak transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	nsv1050535	chr15:53352572-53472957	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	nsv1036751	chr15:53354285-53398679	Enhancers Weak transcription	Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	nsv1039762	chr15:53354285-53414479	Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 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	chr15:53395200-53399600	Weak transcription	Pancreas	Pancrea
2	chr15:53398000-53402600	Weak transcription	H9 Cell Line	embryonic stem cell

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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