Variant report

Variant	rs73326635
Chromosome Location	chr14:81010054-81010055
allele	G/T
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]
rs10132086	1.00[AMR][1000 genomes]
rs10146016	1.00[AMR][1000 genomes]
rs58595334	1.00[AMR][1000 genomes]
rs58978494	1.00[AMR][1000 genomes]
rs60207137	1.00[AMR][1000 genomes]
rs73338970	1.00[AMR][1000 genomes]
rs73338973	1.00[AMR][1000 genomes]
rs73338983	1.00[AMR][1000 genomes]
rs73338987	1.00[AMR][1000 genomes]
rs73338991	1.00[AMR][1000 genomes]
rs73339001	1.00[AMR][1000 genomes]
rs8005950	1.00[AMR][1000 genomes]
rs8014116	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	nsv869348	chr14:80921098-81535754	Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:81003400-81015600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr14:81009000-81012600	Weak transcription	Dnd41	blood
3	chr14:81009600-81010200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr14:81009600-81010400	Enhancers	Brain Substantia Nigra	brain
5	chr14:81010000-81010200	Enhancers	Foreskin Melanocyte Primary Cells skin01	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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