Variant report

Variant	rs967982
Chromosome Location	chr1:104786974-104786975
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs11185410	0.83[ASN][1000 genomes]
rs12133443	0.85[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs12406661	0.83[ASN][1000 genomes]
rs12407649	0.90[ASN][1000 genomes]
rs2317081	0.87[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs2873357	0.87[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs4325136	0.87[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs56868860	0.83[ASN][1000 genomes]
rs6586449	0.87[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs6586450	0.84[AMR][1000 genomes];0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv872072	chr1:104470622-105076810	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv1010903	chr1:104483363-105468941	Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised 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	chr1:104775600-104790200	Weak transcription	Fetal Heart	heart
2	chr1:104785200-104787400	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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