Variant report

Variant	rs4602451
Chromosome Location	chr4:160451466-160451467
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs13114272	0.92[AFR][1000 genomes];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs13117819	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs13145068	0.84[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs1882618	0.88[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs1922647	0.89[AMR][1000 genomes]
rs1922648	0.88[AFR][1000 genomes];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1922649	0.83[EUR][1000 genomes]
rs2244167	0.88[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs2707704	0.82[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs2851775	0.84[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs2851776	0.88[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs2851783	0.90[EUR][1000 genomes]
rs2851784	0.87[AFR][1000 genomes];0.90[EUR][1000 genomes]
rs2851785	0.89[AMR][1000 genomes]
rs2851790	0.87[AFR][1000 genomes];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2851793	0.90[AFR][1000 genomes];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs34775142	0.86[AFR][1000 genomes];0.97[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	nsv1015469	chr4:160389277-160841619	Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv537316	chr4:160389277-160841619	Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 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	chr4:160433200-160458000	Weak transcription	Foreskin Keratinocyte 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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