Variant report

Variant	rs28631891
Chromosome Location	chr1:242109146-242109147
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs28385880	0.86[ASN][1000 genomes]
rs28392846	0.83[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs28413917	0.83[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs28438742	0.83[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs28439042	0.83[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs28444922	0.90[ASN][1000 genomes]
rs28472777	0.81[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs28544076	0.83[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs28615546	0.82[ASN][1000 genomes]
rs28624657	0.81[ASN][1000 genomes]
rs28626680	0.82[ASN][1000 genomes]
rs28661887	0.82[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs28662297	0.82[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs28662847	0.95[ASN][1000 genomes]
rs28710235	0.83[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs28718445	0.82[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs34212793	0.90[ASN][1000 genomes]
rs34518223	0.82[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs35027076	0.83[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs35341580	0.83[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs35363238	0.83[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs35524854	0.83[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs35536186	0.91[ASN][1000 genomes]
rs35892843	0.89[ASN][1000 genomes]
rs35896847	0.81[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs3862974	0.81[ASN][1000 genomes]
rs3862975	0.82[ASN][1000 genomes]
rs59504163	0.82[ASN][1000 genomes]
rs60043862	0.86[ASN][1000 genomes]
rs66861684	0.83[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs67802349	0.91[ASN][1000 genomes]
rs695234	0.82[ASN][1000 genomes]
rs695235	0.82[ASN][1000 genomes]
rs71535345	0.82[ASN][1000 genomes]
rs955535	0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv873368	chr1:241533392-242195928	Weak transcription Active TSS Transcr. at gene 5' and 3' Enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
2	nsv873372	chr1:241690554-242438293	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
3	nsv948409	chr1:241830086-242489705	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
4	nsv1008300	chr1:241886514-242171611	Enhancers Strong transcription Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
5	nsv1008886	chr1:242015591-242176983	Enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
6	esv2750830	chr1:242025098-242303357	Strong transcription Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
7	esv2750831	chr1:242025098-242332959	Enhancers Active TSS Flanking Active TSS Strong transcription Weak transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
8	nsv1002309	chr1:242042242-242295635	Enhancers Strong transcription Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
9	nsv870442	chr1:242105882-242136576	Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:242106400-242113600	Weak transcription	NHDF-Ad	bronchial
2	chr1:242106600-242110200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr1:242108000-242109200	Bivalent/Poised TSS	HepG2	liver
4	chr1:242108800-242109200	Enhancers	A549	lung

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