Variant report

Variant	rs73955104
Chromosome Location	chr2:113712838-113712839
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10166695	1.00[AMR][1000 genomes]
rs10171160	1.00[AMR][1000 genomes]
rs10174364	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10186376	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13384351	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13388479	1.00[AMR][1000 genomes]
rs13391769	0.99[AFR][1000 genomes]
rs13402882	1.00[AMR][1000 genomes]
rs58279921	1.00[AMR][1000 genomes]
rs72942421	1.00[AMR][1000 genomes]
rs72942463	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73955105	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9653424	1.00[AMR][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	nsv532471	chr2:113682449-113862981	ZNF genes & repeats Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
2	nsv997348	chr2:113688093-113986508	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:113711000-113715000	Enhancers	Breast Myoepithelial Primary Cells	Breast
2	chr2:113712600-113714800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr2:113712600-113715000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr2:113712600-113715200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr2:113712600-113715400	Weak transcription	HMEC	breast
6	chr2:113712600-113716200	Weak transcription	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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