Variant report

Variant	rs11716581
Chromosome Location	chr3:24992122-24992123
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 26 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10510548	0.84[ASN][1000 genomes]
rs11129172	0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11713674	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11716868	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12636772	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12636778	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12637240	0.85[EUR][1000 genomes]
rs13061245	0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs13074839	0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs34373965	0.81[EUR][1000 genomes]
rs35025157	0.81[EUR][1000 genomes]
rs35306981	0.93[EUR][1000 genomes]
rs36025902	0.81[ASN][1000 genomes]
rs36052996	0.81[EUR][1000 genomes]
rs55964723	0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs56369650	0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6795387	0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs73034848	0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 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
8	nsv963561	chr3:24990649-24993786	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	n/a	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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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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