Variant report

Variant	rs28386872
Chromosome Location	chr4:69883053-69883054
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 64 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs10006595	0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10019619	0.88[EUR][1000 genomes]
rs10030220	0.95[EUR][1000 genomes]
rs11249520	0.94[EUR][1000 genomes]
rs11725519	0.95[EUR][1000 genomes]
rs12501837	0.92[EUR][1000 genomes]
rs12509175	0.95[EUR][1000 genomes]
rs12512098	0.88[EUR][1000 genomes]
rs13102620	0.93[EUR][1000 genomes]
rs13108709	0.90[EUR][1000 genomes]
rs13116752	0.92[EUR][1000 genomes]
rs13127081	0.95[EUR][1000 genomes]
rs13128177	0.84[EUR][1000 genomes]
rs13140844	0.92[EUR][1000 genomes]
rs13145165	0.88[EUR][1000 genomes]
rs13145304	0.90[EUR][1000 genomes]
rs13147569	0.92[EUR][1000 genomes]
rs13147648	0.93[EUR][1000 genomes]
rs1841055	0.88[EUR][1000 genomes]
rs1902923	0.84[EUR][1000 genomes]
rs2331627	0.88[EUR][1000 genomes]
rs4235106	0.94[EUR][1000 genomes]
rs4235108	0.95[EUR][1000 genomes]
rs4235111	0.92[EUR][1000 genomes]
rs4235112	0.92[EUR][1000 genomes]
rs4299665	0.92[EUR][1000 genomes]
rs4299666	0.92[EUR][1000 genomes]
rs4304032	0.94[EUR][1000 genomes]
rs4305590	0.95[EUR][1000 genomes]
rs4312824	0.92[EUR][1000 genomes]
rs4326076	1.00[ASN][1000 genomes]
rs4336293	1.00[ASN][1000 genomes]
rs4353969	0.93[EUR][1000 genomes]
rs4365792	0.92[EUR][1000 genomes]
rs4440295	0.91[EUR][1000 genomes]
rs4495114	0.93[EUR][1000 genomes]
rs4591680	0.92[EUR][1000 genomes]
rs4604120	1.00[ASN][1000 genomes]
rs4694490	0.87[EUR][1000 genomes]
rs4694491	0.87[EUR][1000 genomes]
rs4694551	0.90[EUR][1000 genomes]
rs61162302	0.91[ASN][1000 genomes]
rs6827511	0.95[EUR][1000 genomes]
rs6828317	0.87[EUR][1000 genomes]
rs6831147	0.81[EUR][1000 genomes]
rs6837000	0.82[EUR][1000 genomes]
rs6839405	0.84[EUR][1000 genomes]
rs6843788	0.87[EUR][1000 genomes]
rs7441736	0.95[EUR][1000 genomes]
rs7673174	0.85[EUR][1000 genomes]
rs7691258	0.85[EUR][1000 genomes]
rs7691445	0.85[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1005513	chr4:69446718-69890307	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
2	nsv999654	chr4:69661415-70132110	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
3	esv3420586	chr4:69680878-70322918	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
4	nsv1067773	chr4:69718248-70715727	ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
5	esv3468151	chr4:69718675-70322776	Enhancers Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
6	esv3468153	chr4:69718675-70322776	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
7	nsv829962	chr4:69786869-69910283	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
8	nsv594582	chr4:69827340-69988378	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
9	esv2757064	chr4:69863174-69901607	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Genic enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
10	nsv980213	chr4:69870183-69893292	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
11	nsv879379	chr4:69878929-69987249	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
12	nsv10521	chr4:69880432-69883223	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:69882000-69883800	Enhancers	HepG2	liver
2	chr4:69883000-69883200	Enhancers	iPS-18 Cell Line	embryonic stem cell
3	chr4:69883000-69883200	Flanking Active TSS	Liver	Liver

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