Variant report

Variant	rs2151782
Chromosome Location	chr14:32301048-32301049
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 151 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:146)

rs_ID	r²[population]
rs10129541	0.81[CHB][hapmap]
rs10132896	0.80[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs10135589	0.82[CHB][hapmap];0.95[CHD][hapmap];0.82[JPT][hapmap]
rs10220330	0.84[YRI][hapmap]
rs11156703	0.82[JPT][hapmap]
rs11156704	0.81[JPT][hapmap]
rs11156707	0.81[CHB][hapmap];0.87[CHD][hapmap];0.81[JPT][hapmap]
rs11156710	0.90[CHB][hapmap]
rs11621147	0.82[JPT][hapmap]
rs11621253	0.85[JPT][hapmap]
rs11621446	0.82[JPT][hapmap]
rs11624178	0.82[CHB][hapmap];0.95[CHD][hapmap];0.82[JPT][hapmap]
rs11624772	0.82[JPT][hapmap]
rs11626466	0.81[JPT][hapmap]
rs11628555	0.82[JPT][hapmap]
rs11628570	0.82[JPT][hapmap]
rs11847399	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12147945	0.82[JPT][hapmap]
rs12431452	0.89[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs12432377	0.89[CEU][hapmap];0.95[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs12433808	0.82[JPT][hapmap]
rs12434452	0.96[ASN][1000 genomes]
rs12434666	0.95[CHB][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs12435286	0.85[CEU][hapmap];0.82[CHB][hapmap];0.95[CHD][hapmap];0.82[JPT][hapmap];1.00[MEX][hapmap];0.89[TSI][hapmap]
rs12435348	0.84[JPT][hapmap]
rs12436193	0.89[ASW][hapmap];0.92[CEU][hapmap];0.95[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.83[LWK][hapmap];0.85[MKK][hapmap];0.86[YRI][hapmap];0.80[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs12436891	0.85[CEU][hapmap];0.86[CHB][hapmap];0.97[CHD][hapmap];0.82[JPT][hapmap]
rs12437209	0.92[CHD][hapmap];0.82[JPT][hapmap]
rs12437440	0.88[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs12586434	0.98[AMR][1000 genomes];0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12589227	0.81[CHB][hapmap];0.82[JPT][hapmap]
rs12590215	0.81[CEU][hapmap];0.86[CHB][hapmap];0.81[JPT][hapmap]
rs12590375	0.81[CEU][hapmap];0.85[CHB][hapmap];0.81[JPT][hapmap]
rs12590836	0.81[CEU][hapmap];0.82[CHB][hapmap];0.81[JPT][hapmap]
rs12878022	0.82[CHB][hapmap];0.95[CHD][hapmap];0.82[JPT][hapmap];1.00[MEX][hapmap];0.87[TSI][hapmap]
rs12878817	0.85[ASN][1000 genomes]
rs12880119	0.84[ASN][1000 genomes]
rs12886260	0.81[JPT][hapmap]
rs12886280	0.95[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.88[MEX][hapmap];0.86[ASN][1000 genomes]
rs12886367	0.82[JPT][hapmap]
rs12887004	0.80[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs12890318	0.81[JPT][hapmap]
rs12895480	0.92[CHD][hapmap];0.82[JPT][hapmap]
rs12895565	0.90[CHD][hapmap];0.82[JPT][hapmap]
rs1430425	0.96[CEU][hapmap];0.86[CHB][hapmap];0.81[JPT][hapmap];0.88[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs1430431	0.82[CHB][hapmap];0.82[JPT][hapmap]
rs1443143	0.92[CHD][hapmap];0.82[JPT][hapmap]
rs1443144	0.92[CHD][hapmap];0.82[JPT][hapmap]
rs1545275	0.82[JPT][hapmap]
rs1560426	0.82[JPT][hapmap]
rs17098061	0.82[JPT][hapmap]
rs17098152	0.81[CHB][hapmap];0.92[CHD][hapmap];0.82[JPT][hapmap]
rs17379143	0.89[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs17390827	0.81[CHB][hapmap];0.82[JPT][hapmap]
rs17463975	0.85[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1822355	0.81[CHB][hapmap];0.82[JPT][hapmap]
rs1897141	0.82[CHB][hapmap];0.92[CHD][hapmap];0.82[JPT][hapmap]
rs1897142	0.86[CHB][hapmap];0.82[JPT][hapmap]
rs1954440	0.92[CHD][hapmap];0.82[JPT][hapmap]
rs1954441	0.82[CHB][hapmap];0.95[CHD][hapmap];0.82[JPT][hapmap]
rs2082167	0.83[ASN][1000 genomes]
rs2105275	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2115956	0.92[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs2120140	0.81[CHB][hapmap];0.95[CHD][hapmap];0.82[JPT][hapmap]
rs2120142	0.82[CHB][hapmap];0.81[JPT][hapmap]
rs2153560	0.90[CHD][hapmap];0.82[JPT][hapmap]
rs2226057	0.81[JPT][hapmap]
rs2378936	0.92[CHD][hapmap];0.82[JPT][hapmap]
rs2378940	0.82[CHB][hapmap];0.87[CHD][hapmap];0.82[JPT][hapmap]
rs2378944	0.92[CHD][hapmap];0.82[JPT][hapmap]
rs2378945	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs28788900	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs35588979	0.82[ASN][1000 genomes]
rs35650602	0.84[ASN][1000 genomes]
rs35722809	0.86[ASN][1000 genomes]
rs35746551	0.83[ASN][1000 genomes]
rs35875023	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs36020968	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4514587	0.85[ASN][1000 genomes]
rs4619303	0.92[CHD][hapmap];0.82[JPT][hapmap]
rs4981111	0.81[CHB][hapmap];0.82[JPT][hapmap]
rs4981112	0.82[CHB][hapmap];0.95[CHD][hapmap];0.82[JPT][hapmap];0.95[MEX][hapmap];0.87[TSI][hapmap]
rs4981119	0.85[JPT][hapmap]
rs4981120	0.85[CHB][hapmap];0.82[JPT][hapmap]
rs4981122	0.82[JPT][hapmap]
rs4981123	0.86[CHB][hapmap];0.82[JPT][hapmap]
rs4981124	0.92[CEU][hapmap];0.90[CHB][hapmap];0.82[JPT][hapmap]
rs4981126	0.86[CHB][hapmap];0.95[CHD][hapmap];0.83[GIH][hapmap];0.86[JPT][hapmap]
rs4981127	0.98[AMR][1000 genomes];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4981871	0.85[CHB][hapmap];0.82[JPT][hapmap]
rs4981874	0.82[CHB][hapmap];0.82[JPT][hapmap]
rs4981876	0.82[JPT][hapmap]
rs4981880	0.82[CHB][hapmap]
rs4981891	0.82[JPT][hapmap]
rs4981894	0.82[JPT][hapmap]
rs4981897	0.85[CEU][hapmap];0.82[CHB][hapmap];0.86[JPT][hapmap]
rs4981900	0.82[JPT][hapmap]
rs4981902	0.82[CHB][hapmap];0.81[JPT][hapmap]
rs4981904	0.82[CHB][hapmap];0.92[CHD][hapmap];0.82[JPT][hapmap]
rs4981905	0.92[CEU][hapmap];0.82[CHB][hapmap];0.82[JPT][hapmap]
rs4981906	0.82[JPT][hapmap]
rs4981909	0.89[CEU][hapmap];0.86[CHB][hapmap];0.82[JPT][hapmap]
rs4981910	0.89[CEU][hapmap];0.91[CHB][hapmap];0.82[JPT][hapmap]
rs4981911	0.81[CHB][hapmap];0.82[JPT][hapmap]
rs4981912	0.81[CHB][hapmap];0.85[JPT][hapmap]
rs4981915	0.85[ASN][1000 genomes]
rs4981916	0.85[ASN][1000 genomes]
rs56001625	0.85[ASN][1000 genomes]
rs56293516	0.97[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs60006676	0.86[ASN][1000 genomes]
rs61421033	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs61996360	0.86[ASN][1000 genomes]
rs6571459	0.92[CHD][hapmap];0.82[JPT][hapmap]
rs6571468	0.89[ASW][hapmap];0.92[CEU][hapmap];0.95[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.83[LWK][hapmap];0.82[MKK][hapmap];0.86[ASN][1000 genomes]
rs68170651	0.86[ASN][1000 genomes]
rs7141411	0.89[CEU][hapmap];0.91[CHB][hapmap];1.00[CHD][hapmap];0.81[JPT][hapmap]
rs7141900	0.85[CEU][hapmap];0.91[CHB][hapmap];0.86[JPT][hapmap];0.87[AMR][1000 genomes];0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7142429	0.89[CEU][hapmap];0.95[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs7144386	0.86[ASN][1000 genomes]
rs7145749	0.86[CHB][hapmap];0.95[CHD][hapmap];0.85[GIH][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs7145823	0.85[CEU][hapmap];0.95[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.93[TSI][hapmap];0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7148166	0.89[CEU][hapmap];0.82[CHB][hapmap];0.95[CHD][hapmap];0.82[JPT][hapmap]
rs7149151	0.81[JPT][hapmap]
rs7153475	0.82[JPT][hapmap]
rs7156902	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7157366	0.82[JPT][hapmap]
rs7158021	0.82[CHB][hapmap];0.95[CHD][hapmap];0.82[JPT][hapmap]
rs7159758	0.96[CEU][hapmap];0.82[CHB][hapmap];0.95[CHD][hapmap];0.91[GIH][hapmap];0.82[JPT][hapmap];0.95[MEX][hapmap];0.81[MKK][hapmap];0.91[TSI][hapmap];0.88[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs720954	0.82[JPT][hapmap]
rs7492643	0.81[CHB][hapmap];0.95[CHD][hapmap];0.82[JPT][hapmap]
rs7493492	0.84[JPT][hapmap]
rs767333	0.92[CHD][hapmap];0.82[JPT][hapmap]
rs8006164	0.82[CHB][hapmap];0.81[JPT][hapmap]
rs8010580	0.84[CHB][hapmap]
rs8010603	0.92[CEU][hapmap];0.81[CHB][hapmap];0.95[CHD][hapmap];0.91[GIH][hapmap];0.82[JPT][hapmap];0.91[MEX][hapmap];0.91[TSI][hapmap];0.87[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs8013530	0.81[CHB][hapmap];0.95[CHD][hapmap];0.82[JPT][hapmap]
rs8014386	0.80[CHB][hapmap];0.84[JPT][hapmap]
rs8016912	0.82[CHB][hapmap];0.95[CHD][hapmap];0.82[JPT][hapmap]
rs8018532	0.86[ASN][1000 genomes]
rs8018901	0.89[CEU][hapmap];0.95[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs8019296	0.82[CHB][hapmap];0.81[JPT][hapmap]
rs8020397	0.92[CHD][hapmap];0.82[JPT][hapmap]
rs8021918	0.84[MEX][hapmap]
rs8022541	0.82[JPT][hapmap]
rs891468	0.87[CEU][hapmap];0.83[CHB][hapmap];0.89[JPT][hapmap]
rs919521	0.82[JPT][hapmap]

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	nsv564180	chr14:31958566-32368934	Strong transcription Enhancers Transcr. at gene 5' and 3' Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
2	nsv564181	chr14:31958761-32363980	Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Active TSS Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
3	nsv564182	chr14:32110519-32584337	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
4	nsv1046526	chr14:32110537-32567426	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
5	nsv901593	chr14:32282564-32350371	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA target site	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:23 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:32250600-32322400	Weak transcription	Primary T helper cells fromperipheralblood	blood
2	chr14:32281800-32330200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
3	chr14:32291000-32310400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr14:32293200-32303600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
5	chr14:32294200-32328800	Weak transcription	Ovary	ovary
6	chr14:32294600-32304200	Weak transcription	HSMM	muscle
7	chr14:32294800-32328000	Weak transcription	Left Ventricle	heart
8	chr14:32295000-32332800	Weak transcription	Primary hematopoietic stem cells	blood
9	chr14:32297000-32304000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr14:32297000-32306600	Weak transcription	Primary B cells from peripheral blood	blood
11	chr14:32297200-32303800	Weak transcription	HepG2	liver
12	chr14:32297400-32325800	Weak transcription	Primary B cells from cord blood	blood
13	chr14:32298200-32322000	Weak transcription	Primary T cells from cord blood	blood
14	chr14:32298400-32303800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr14:32298400-32304200	Weak transcription	Fetal Kidney	kidney
16	chr14:32299000-32303000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr14:32299000-32303800	Weak transcription	Osteobl	bone
18	chr14:32299000-32325800	Weak transcription	Fetal Stomach	stomach
19	chr14:32299200-32303800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr14:32299400-32303800	Weak transcription	Muscle Satellite Cultured Cells	--
21	chr14:32299800-32302200	Weak transcription	Fetal Brain Male	brain
22	chr14:32300800-32301400	Enhancers	HUVEC	blood vessel
23	chr14:32300800-32302400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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