Variant report

Variant	rs62520981
Chromosome Location	chr8:69685261-69685262
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs10099614	0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10957447	0.87[ASN][1000 genomes]
rs11993861	0.82[ASN][1000 genomes]
rs11994264	0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11995110	0.87[ASN][1000 genomes]
rs12675214	0.86[ASN][1000 genomes]
rs12675220	0.86[ASN][1000 genomes]
rs34283177	0.87[ASN][1000 genomes]
rs4374973	0.86[ASN][1000 genomes]
rs4401840	0.86[ASN][1000 genomes]
rs5022152	0.86[ASN][1000 genomes]
rs6983604	0.81[ASN][1000 genomes]
rs6984482	0.86[ASN][1000 genomes]
rs6998182	0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7016624	0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs73270234	0.88[ASN][1000 genomes]
rs7461173	0.86[ASN][1000 genomes]
rs7464182	0.86[ASN][1000 genomes]
rs7464209	0.86[ASN][1000 genomes]
rs7817788	0.86[ASN][1000 genomes]
rs7833828	0.86[ASN][1000 genomes]
rs7834286	0.83[ASN][1000 genomes]
rs7843991	0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv831349	chr8:69555461-69733515	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
2	nsv465703	chr8:69641287-69814578	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv611462	chr8:69641287-69814578	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv890986	chr8:69647914-69704366	Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv1017131	chr8:69676989-69792515	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv519549	chr8:69682388-69687852	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 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	chr8:69675200-69686200	Weak transcription	Fetal Lung	lung
2	chr8:69683000-69688000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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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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