Variant report

Variant	rs182116
Chromosome Location	chr5:5077841-5077842
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:59)

rs_ID	r²[population]
rs10077722	0.91[AMR][1000 genomes]
rs1021761	0.94[EUR][1000 genomes]
rs1021762	0.94[EUR][1000 genomes]
rs1021763	0.94[EUR][1000 genomes]
rs10474784	0.81[AMR][1000 genomes]
rs10475281	0.81[AFR][1000 genomes];0.88[AMR][1000 genomes]
rs1158328	0.94[EUR][1000 genomes]
rs12654635	0.86[AMR][1000 genomes]
rs1351287	0.94[EUR][1000 genomes]
rs1382896	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1382898	0.94[EUR][1000 genomes]
rs1501638	0.94[EUR][1000 genomes]
rs1501639	0.94[EUR][1000 genomes]
rs156252	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs172016	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs172050	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1812836	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1818107	0.94[EUR][1000 genomes]
rs1842240	0.89[AMR][1000 genomes]
rs2008213	0.94[EUR][1000 genomes]
rs2008214	0.94[EUR][1000 genomes]
rs2015936	0.94[EUR][1000 genomes]
rs2015937	0.94[EUR][1000 genomes]
rs2619809	0.94[EUR][1000 genomes]
rs2619814	0.94[EUR][1000 genomes]
rs2652053	0.94[EUR][1000 genomes]
rs2652054	0.94[EUR][1000 genomes]
rs2652055	0.91[EUR][1000 genomes]
rs2652057	0.94[EUR][1000 genomes]
rs2652058	0.94[EUR][1000 genomes]
rs2652059	0.94[EUR][1000 genomes]
rs2652060	0.94[EUR][1000 genomes]
rs270628	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs270629	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs270631	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs270632	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs270633	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs270634	0.84[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs270635	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs270636	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs270637	0.82[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs270638	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs270639	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs270641	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs270644	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs272183	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs272202	0.94[EUR][1000 genomes]
rs272203	0.94[EUR][1000 genomes]
rs272204	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4701671	0.83[AMR][1000 genomes]
rs899552	0.94[EUR][1000 genomes]
rs899553	0.94[EUR][1000 genomes]
rs899554	0.94[EUR][1000 genomes]
rs899555	0.94[EUR][1000 genomes]
rs899556	0.94[EUR][1000 genomes]
rs905153	0.94[EUR][1000 genomes]
rs905154	0.94[EUR][1000 genomes]
rs970529	0.94[EUR][1000 genomes]
rs977341	0.94[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1021653	chr5:4932992-5201887	Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS Weak transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	esv2757980	chr5:4980876-5184615	Enhancers Bivalent/Poised TSS Strong transcription ZNF genes & repeats Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
3	esv2759318	chr5:4980876-5184615	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
4	nsv1024784	chr5:4980979-5391231	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS 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	17 gene(s)	inside rSNPs	diseases
5	nsv830194	chr5:5002459-5187667	Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:5072000-5078200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr5:5075600-5079000	Enhancers	H1 Cell Line	embryonic stem cell
3	chr5:5075600-5079400	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr5:5075800-5078200	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr5:5076000-5078400	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr5:5076000-5079400	Enhancers	HUES6 Cell Line	embryonic stem cell
7	chr5:5076000-5079400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr5:5077000-5079600	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr5:5077200-5078000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr5:5077600-5078000	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr5:5077800-5078200	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr5:5077800-5079400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
13	chr5:5077800-5079600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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