Variant report

Variant	rs62249355
Chromosome Location	chr3:34817489-34817490
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs62249356	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs62251603	0.88[EUR][1000 genomes]
rs62251609	0.84[EUR][1000 genomes]
rs62251610	0.81[EUR][1000 genomes]
rs62251611	0.84[EUR][1000 genomes]
rs62251612	0.81[EUR][1000 genomes]
rs62251613	0.84[EUR][1000 genomes]
rs62251614	0.81[EUR][1000 genomes]
rs62251615	0.81[EUR][1000 genomes]
rs62251616	0.81[EUR][1000 genomes]
rs62251617	0.81[EUR][1000 genomes]
rs62251619	0.84[EUR][1000 genomes]
rs62251620	0.84[EUR][1000 genomes]
rs62251621	0.81[EUR][1000 genomes]
rs7652586	0.84[EUR][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	nsv834654	chr3:34747802-34916657	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv834655	chr3:34752929-34898824	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
3	esv3415700	chr3:34806371-34914306	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	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	chr3:34814800-34821800	Weak transcription	ES-I3 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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