Variant report

Variant	rs6798808
Chromosome Location	chr3:24990630-24990631
allele	C/G
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:17)

rs_ID	r²[population]
rs11710017	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs13098681	0.80[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2363524	0.86[EUR][1000 genomes]
rs2363526	0.87[EUR][1000 genomes]
rs2363528	0.87[EUR][1000 genomes]
rs2363529	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2363530	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4858667	0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6772493	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs6779838	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs6792021	0.81[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs937269	0.82[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs9833261	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs9843826	0.87[EUR][1000 genomes]
rs9847199	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9881799	0.82[EUR][1000 genomes]
rs9883836	0.87[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	nsv589953	chr3:24909003-25004804	Enhancers Weak transcription Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv876630	chr3:24911917-25066711	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv834644	chr3:24936987-25112610	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv460482	chr3:24966768-25071616	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv589954	chr3:24966768-25071616	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv1008974	chr3:24968434-24992497	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv589955	chr3:24987823-25113358	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 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	chr3:24979200-24998400	Weak transcription	Right Atrium	heart
2	chr3:24987000-24996800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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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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