Variant report

Variant	rs10102735
Chromosome Location	chr8:110827747-110827748
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs10086058	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10091536	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10091583	1.00[ASN][1000 genomes]
rs10097751	1.00[ASN][1000 genomes]
rs10101288	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs28583803	1.00[ASN][1000 genomes]
rs28593097	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28610171	1.00[AMR][1000 genomes]
rs28623195	1.00[ASN][1000 genomes]
rs60387056	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7825511	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7825600	1.00[AMR][1000 genomes]
rs7825601	1.00[AMR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1033321	chr8:110826297-111131801	Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 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	chr8:110821800-110828800	Weak transcription	Fetal Lung	lung

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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