Variant report

Variant	rs7445576
Chromosome Location	chr5:154036902-154036903
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10875591	0.86[ASN][1000 genomes]
rs11167697	0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs11167698	0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12515092	0.89[ASN][1000 genomes]
rs12652072	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1811291	0.86[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs1972616	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2396995	0.86[ASN][1000 genomes]
rs28794278	0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4958753	0.83[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs4958758	0.82[ASN][1000 genomes]
rs59189695	0.85[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs6580099	0.83[ASN][1000 genomes]
rs72797553	0.83[ASN][1000 genomes]
rs7444282	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs918365	0.82[ASN][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	esv3401644	chr5:153898681-154058368	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 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	chr5:154035000-154040600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr5:154035200-154040800	Weak transcription	K562	blood

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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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