Variant report

Variant	rs28401747
Chromosome Location	chr5:79596333-79596334
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10052506	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10054681	0.96[ASN][1000 genomes]
rs10054927	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10055300	0.96[ASN][1000 genomes]
rs10056958	0.96[ASN][1000 genomes]
rs10070311	0.95[ASN][1000 genomes]
rs10070958	1.00[ASN][1000 genomes]
rs10071189	0.96[ASN][1000 genomes]
rs10075519	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10474013	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs10474015	0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10474614	0.96[ASN][1000 genomes]
rs12332228	0.94[ASN][1000 genomes]
rs12332699	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13361029	0.96[ASN][1000 genomes]
rs28366631	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28424275	1.00[ASN][1000 genomes]
rs28520641	0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs28605690	0.85[AFR][1000 genomes];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6453512	0.96[ASN][1000 genomes]
rs72778013	0.96[ASN][1000 genomes]
rs72778033	1.00[ASN][1000 genomes]
rs72778039	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9293811	0.99[ASN][1000 genomes]
rs9293814	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs950788	0.96[ASN][1000 genomes]
rs9654436	0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv948807	chr5:79549207-79805765	Genic enhancers Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
2	nsv518480	chr5:79586085-79748382	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
3	nsv980690	chr5:79591958-79614381	Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:79595800-79596600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr5:79596200-79596400	Bivalent Enhancer	K562	blood
3	chr5:79596200-79598400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr5:79596200-79598400	Weak transcription	Gastric	stomach

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