Variant report

Variant	rs6453091
Chromosome Location	chr5:74210986-74210987
allele	A/G
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]
rs10942723	0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11740894	0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11745011	0.80[ASN][1000 genomes]
rs11745016	0.80[ASN][1000 genomes]
rs11745686	0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11746386	0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12519932	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1455786	0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs55979253	0.80[ASN][1000 genomes]
rs56831970	0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs58925145	0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs62367818	0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6894292	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7700681	0.86[ASN][1000 genomes]
rs7719022	0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7721009	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7722489	0.81[ASN][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	nsv518286	chr5:74169045-74243120	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv830352	chr5:74189495-74337944	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 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	chr5:74210200-74214000	Enhancers	Stomach Mucosa	stomach
2	chr5:74210400-74213800	Enhancers	HepG2	liver

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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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