Variant report

Variant	rs73592772
Chromosome Location	chr10:4418601-4418602
allele	A/G
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:12)

rs_ID	r²[population]
rs1028837	1.00[EUR][1000 genomes]
rs11816582	1.00[EUR][1000 genomes]
rs1926812	1.00[EUR][1000 genomes]
rs2209686	1.00[EUR][1000 genomes]
rs4285784	1.00[EUR][1000 genomes]
rs4382802	1.00[EUR][1000 genomes]
rs7081095	1.00[EUR][1000 genomes]
rs73590796	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73592723	0.82[AFR][1000 genomes]
rs73592732	1.00[EUR][1000 genomes]
rs73592770	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73592774	1.00[EUR][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	nsv894786	chr10:4385379-4441989	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv894787	chr10:4385379-4857717	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	20 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	chr10:4416200-4424000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr10:4418600-4418800	Enhancers	Foreskin Melanocyte Primary Cells skin03	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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