Variant report

Variant	rs3025061
Chromosome Location	chr11:102713675-102713676
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 5 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs1051121	1.00[CEU][hapmap]
rs28381677	0.82[AFR][1000 genomes]
rs3025077	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6590992	0.82[AFR][1000 genomes];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	nsv898335	chr11:102682285-102866158	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:102707800-102713800	Weak transcription	NHDF-Ad	bronchial
2	chr11:102711600-102715200	Weak transcription	Stomach Mucosa	stomach
3	chr11:102713200-102714600	Enhancers	Breast Myoepithelial Primary Cells	Breast
4	chr11:102713400-102714000	Enhancers	NHEK	skin

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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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