Variant report

Variant	rs72760302
Chromosome Location	chr5:58025448-58025449
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:58022097..58023766-chr5:58024865..58027239,2	K562	blood:

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs10038836	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs10055378	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10055388	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10058168	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10060872	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10066482	0.82[EUR][1000 genomes]
rs10070606	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs10078211	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10079823	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10471459	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10472069	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10472070	0.92[AMR][1000 genomes];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10514876	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10514877	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11750820	0.83[EUR][1000 genomes]
rs11750857	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12152774	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12153291	0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs13354829	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs13436622	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs17282012	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs17348080	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2194037	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs35694320	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6877247	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs72760285	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs72760294	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs753219	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs753220	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9283719	0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9292171	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9292173	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 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
3	nsv830311	chr5:57912546-58105636	Enhancers Active TSS Strong transcription Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	esv3391589	chr5:58025195-58026393	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:58022800-58029000	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr5:58025000-58026600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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