Variant report

Variant	rs4452435
Chromosome Location	chr4:102337706-102337707
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 131 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:123)

rs_ID	r²[population]
rs10007821	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10007902	1.00[CEU][hapmap];0.83[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10009249	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10017730	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10027194	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1031033	0.96[CEU][hapmap];0.86[JPT][hapmap];0.82[TSI][hapmap]
rs1031034	0.96[CEU][hapmap];0.86[JPT][hapmap];0.80[MEX][hapmap];0.83[TSI][hapmap]
rs10433980	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10433981	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10433982	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10433984	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11097747	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1125180	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12499349	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12642424	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12649313	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13108283	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs13109704	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs13132496	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13135111	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs13135270	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs13135441	0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs13143896	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs13148622	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs13148645	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1348161	0.96[CEU][hapmap];0.91[CHD][hapmap];0.86[JPT][hapmap];0.87[MEX][hapmap];0.83[TSI][hapmap]
rs1372242	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1441433	0.81[JPT][hapmap]
rs1476159	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1530259	0.96[CEU][hapmap];0.91[CHD][hapmap];0.86[JPT][hapmap];0.83[TSI][hapmap]
rs1549513	1.00[CEU][hapmap];0.83[CHB][hapmap];0.83[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.84[MEX][hapmap];0.94[TSI][hapmap];0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1549514	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1549515	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1549516	1.00[CEU][hapmap];0.83[CHB][hapmap];0.83[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.84[MEX][hapmap];0.94[TSI][hapmap];0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1583911	0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1596061	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1822168	0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1822169	0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1946946	0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2013410	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2044044	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs210811	0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2119591	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2119592	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2119593	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2119595	0.86[EUR][1000 genomes]
rs2119596	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2433297	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2433298	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2433299	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2433311	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2583385	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2583386	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2583387	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2583389	0.96[CEU][hapmap];0.86[JPT][hapmap];0.81[EUR][1000 genomes]
rs2583392	0.96[CEU][hapmap];0.86[JPT][hapmap]
rs2583394	0.96[CEU][hapmap];0.91[CHD][hapmap];0.86[JPT][hapmap];0.87[MEX][hapmap];0.83[TSI][hapmap]
rs2583395	0.96[CEU][hapmap];0.91[CHD][hapmap];0.86[JPT][hapmap];0.87[MEX][hapmap];0.83[TSI][hapmap]
rs2583398	0.96[CEU][hapmap];0.91[CHD][hapmap];0.86[JPT][hapmap];0.80[TSI][hapmap]
rs2583399	0.96[CEU][hapmap];0.91[CHD][hapmap];0.86[JPT][hapmap];0.87[MEX][hapmap];0.83[TSI][hapmap]
rs2583406	0.81[JPT][hapmap]
rs2850326	0.96[CEU][hapmap];0.86[JPT][hapmap]
rs2850328	0.80[ASN][1000 genomes]
rs2850329	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2850330	0.84[EUR][1000 genomes]
rs2850331	0.84[EUR][1000 genomes]
rs2850333	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2850334	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2850356	0.80[JPT][hapmap]
rs2850366	0.96[CEU][hapmap]
rs2850367	0.96[CEU][hapmap];0.86[JPT][hapmap]
rs2850369	0.96[CEU][hapmap]
rs2850370	0.96[CEU][hapmap];0.91[CHD][hapmap];0.86[JPT][hapmap];0.83[TSI][hapmap]
rs2850371	0.96[CEU][hapmap];0.91[CHD][hapmap];0.86[JPT][hapmap];0.87[MEX][hapmap];0.83[TSI][hapmap]
rs2866376	0.81[EUR][1000 genomes]
rs293207	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs293209	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs293210	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs293211	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs293212	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs293213	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs293214	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs293215	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs293216	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs293217	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4235418	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4312760	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4574415	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4698957	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4699209	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4699210	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4699211	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4699212	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4699213	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4699214	0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs61478357	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6532928	0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6532929	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6532930	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6532931	0.83[EUR][1000 genomes]
rs6532934	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6532935	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6816400	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6824603	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6825658	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6842703	0.81[EUR][1000 genomes]
rs6845368	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6846097	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6847376	0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6852377	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6856370	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7668224	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7670594	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7670922	0.80[AMR][1000 genomes];0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7677595	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7687487	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7690316	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs833945	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs833946	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs833948	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs833949	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs833955	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs920559	0.81[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv931418	chr4:101500167-102443207	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
2	nsv999741	chr4:102009017-102454115	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases
3	nsv537199	chr4:102009017-102454115	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases
4	nsv1004766	chr4:102009017-102713765	Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	8 gene(s)	inside rSNPs	diseases
5	nsv537200	chr4:102009017-102713765	Weak transcription Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	8 gene(s)	inside rSNPs	diseases
6	nsv1011351	chr4:102056024-102450302	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
7	nsv879676	chr4:102202285-102340930	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
8	nsv1009302	chr4:102335072-102410893	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs4452435	AP001816.1	cis	Whole Blood	GTEx
rs4452435	FLJ20021	cis	multi-tissue	Pritchard

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:102335800-102337800	Enhancers	Breast Myoepithelial Primary Cells	Breast
2	chr4:102336200-102337800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
3	chr4:102336400-102339600	Weak transcription	HUVEC	blood vessel
4	chr4:102336400-102340200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
5	chr4:102336400-102341600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
6	chr4:102336800-102340400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr4:102336800-102341400	Weak transcription	Adipose Nuclei	Adipose
8	chr4:102337200-102337800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr4:102337200-102337800	Enhancers	Right Ventricle	heart
10	chr4:102337200-102338400	Bivalent Enhancer	Primary T killer naive cells fromperipheralblood	blood
11	chr4:102337200-102338800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
12	chr4:102337200-102339200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr4:102337600-102338000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr4:102337600-102338400	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
15	chr4:102337600-102338600	Bivalent Enhancer	Primary T helper naive cells from peripheral blood	blood
16	chr4:102337600-102338600	Bivalent Enhancer	Primary T helper naive cells fromperipheralblood	blood
17	chr4:102337600-102338800	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
18	chr4:102337600-102340600	Enhancers	Dnd41	blood

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