Variant report

Variant	rs1607025
Chromosome Location	chr5:58135905-58135906
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]
rs1345640	1.00[AMR][1000 genomes]
rs1363336	1.00[AMR][1000 genomes]
rs1422227	1.00[AMR][1000 genomes]
rs1607026	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16888328	1.00[AMR][1000 genomes]
rs16888337	1.00[AMR][1000 genomes]
rs16888391	1.00[AMR][1000 genomes]
rs16888394	1.00[AMR][1000 genomes]
rs16888470	1.00[AMR][1000 genomes]
rs16888696	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16888929	1.00[AMR][1000 genomes]
rs56784376	0.82[AFR][1000 genomes]
rs59671367	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	esv2830363	chr5:57893949-58555491	Weak transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
2	nsv1029145	chr5:57905821-58141221	Active TSS Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:58131800-58140800	Weak transcription	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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