Variant report

Variant	rs8125556
Chromosome Location	chr20:41066163-41066164
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs1125550	0.80[ASN][1000 genomes]
rs1883269	0.86[EUR][1000 genomes]
rs2142795	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2179217	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2205945	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2425491	0.86[EUR][1000 genomes]
rs2425494	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2425496	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2425498	0.90[EUR][1000 genomes]
rs4810355	0.87[EUR][1000 genomes]
rs6016792	0.83[ASN][1000 genomes]
rs6030215	0.81[EUR][1000 genomes]
rs6030224	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6030233	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6072745	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7268459	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs932320	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2751913	chr20:40422982-41269321	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
2	nsv532516	chr20:40451059-41097155	Weak transcription Strong transcription Enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
3	nsv833987	chr20:41007663-41184914	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	9 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	chr20:41042000-41070000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr20:41062200-41066400	Weak transcription	Fetal Muscle Leg	muscle

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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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