Variant report

Variant	rs7149154
Chromosome Location	chr14:37516715-37516716
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:37513736..37515871-chr14:37516258..37519151,2	K562	blood:
2	chr14:37508396..37513083-chr14:37513414..37517203,5	MCF-7	breast:

Extended variants
information (count: 110 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:105)

rs_ID	r²[population]
rs10047907	0.91[CEU][hapmap];0.82[EUR][1000 genomes]
rs10047908	0.91[CEU][hapmap];0.83[GIH][hapmap];0.82[EUR][1000 genomes]
rs10131531	0.81[EUR][1000 genomes]
rs10133042	0.95[CEU][hapmap];0.98[EUR][1000 genomes]
rs10133820	0.93[ASN][1000 genomes]
rs10135756	0.98[EUR][1000 genomes]
rs10136755	1.00[ASW][hapmap];0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.97[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10136870	0.91[CEU][hapmap];0.99[EUR][1000 genomes]
rs10137539	0.86[CHB][hapmap];1.00[JPT][hapmap];0.86[MEX][hapmap];0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10137595	0.91[CEU][hapmap];0.82[EUR][1000 genomes]
rs10137611	0.95[CEU][hapmap];0.89[GIH][hapmap];0.99[EUR][1000 genomes]
rs10139726	1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10140136	1.00[CHB][hapmap];0.82[CHD][hapmap];0.84[GIH][hapmap];0.90[JPT][hapmap];0.80[ASN][1000 genomes]
rs10143832	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10148080	0.91[CEU][hapmap];0.81[EUR][1000 genomes]
rs10148097	0.81[EUR][1000 genomes]
rs10148311	0.91[CEU][hapmap];0.81[GIH][hapmap];0.82[EUR][1000 genomes]
rs10148426	0.82[EUR][1000 genomes]
rs10483486	1.00[CHB][hapmap];1.00[CHD][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap];0.95[TSI][hapmap];0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11156932	0.85[EUR][1000 genomes]
rs11848427	1.00[CHB][hapmap];0.90[JPT][hapmap]
rs12433348	0.91[CEU][hapmap];0.82[EUR][1000 genomes]
rs12879089	0.86[CHB][hapmap];1.00[JPT][hapmap]
rs12879259	1.00[CHB][hapmap];1.00[CHD][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap];0.95[TSI][hapmap];0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12883863	0.86[CHB][hapmap];0.91[CHD][hapmap];1.00[JPT][hapmap]
rs12889779	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12892230	0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12892728	0.99[EUR][1000 genomes]
rs12893236	0.86[CHB][hapmap]
rs12894067	0.91[CEU][hapmap];0.83[EUR][1000 genomes]
rs12894251	0.85[EUR][1000 genomes]
rs12897058	0.99[EUR][1000 genomes]
rs12897101	0.86[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13353107	0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1467484	0.81[EUR][1000 genomes]
rs1467485	0.90[CEU][hapmap];0.81[EUR][1000 genomes]
rs1467486	0.90[CEU][hapmap];0.81[EUR][1000 genomes]
rs1467487	0.81[EUR][1000 genomes]
rs1467489	0.91[CEU][hapmap];0.81[EUR][1000 genomes]
rs1467490	0.90[CEU][hapmap];0.82[EUR][1000 genomes]
rs1467491	0.95[CEU][hapmap];0.81[EUR][1000 genomes]
rs1467492	0.81[EUR][1000 genomes]
rs1467493	0.95[CEU][hapmap];0.81[EUR][1000 genomes]
rs1535239	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1555333	0.81[EUR][1000 genomes]
rs17106133	0.85[EUR][1000 genomes]
rs17106164	0.86[CHB][hapmap];1.00[CHD][hapmap];0.89[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.87[TSI][hapmap];0.95[ASN][1000 genomes]
rs17554224	1.00[JPT][hapmap]
rs1950816	0.81[CEU][hapmap]
rs1956422	0.91[CEU][hapmap];0.84[EUR][1000 genomes]
rs1956425	0.95[CEU][hapmap];0.82[EUR][1000 genomes]
rs2022726	0.80[ASN][1000 genomes]
rs2180600	0.95[CEU][hapmap];0.89[GIH][hapmap];0.97[TSI][hapmap];0.97[EUR][1000 genomes]
rs2415374	0.80[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2415375	0.97[EUR][1000 genomes]
rs2415376	0.97[EUR][1000 genomes]
rs2415377	0.83[EUR][1000 genomes]
rs2415378	0.91[CEU][hapmap];0.82[EUR][1000 genomes]
rs28437272	0.85[EUR][1000 genomes]
rs28466578	0.97[EUR][1000 genomes]
rs34592617	0.98[EUR][1000 genomes]
rs35341876	0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs35844261	0.85[EUR][1000 genomes]
rs36105433	0.99[EUR][1000 genomes]
rs4328351	0.81[EUR][1000 genomes]
rs4408459	0.95[CEU][hapmap];0.84[GIH][hapmap];0.97[TSI][hapmap];0.98[EUR][1000 genomes]
rs58079830	0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6571773	0.91[CEU][hapmap];0.85[EUR][1000 genomes]
rs6571774	0.85[EUR][1000 genomes]
rs6571775	0.86[CEU][hapmap];0.85[EUR][1000 genomes]
rs6571776	0.86[CHB][hapmap];1.00[CHD][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.95[TSI][hapmap];0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6571777	0.86[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs6571778	0.89[CEU][hapmap];0.83[EUR][1000 genomes]
rs6571779	0.81[EUR][1000 genomes]
rs6571780	0.91[CEU][hapmap];0.82[EUR][1000 genomes]
rs7141528	0.91[CEU][hapmap]
rs7142225	0.91[CEU][hapmap];0.85[EUR][1000 genomes]
rs714268	0.91[CEU][hapmap];0.85[EUR][1000 genomes]
rs714269	0.98[EUR][1000 genomes]
rs7143414	0.86[CHB][hapmap];1.00[CHD][hapmap];0.91[GIH][hapmap];1.00[JPT][hapmap];0.86[MEX][hapmap];0.95[TSI][hapmap];0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7145475	0.86[CHB][hapmap];1.00[JPT][hapmap]
rs7146275	0.82[EUR][1000 genomes]
rs7149490	0.95[CEU][hapmap];0.89[GIH][hapmap];0.97[TSI][hapmap];0.99[EUR][1000 genomes]
rs7151191	1.00[CHB][hapmap];0.91[CHD][hapmap];1.00[JPT][hapmap]
rs7153530	0.91[CEU][hapmap];0.81[EUR][1000 genomes]
rs7160964	0.85[EUR][1000 genomes]
rs7359049	0.91[CEU][hapmap];0.82[EUR][1000 genomes]
rs7359050	0.82[EUR][1000 genomes]
rs7359156	1.00[CHB][hapmap];0.82[CHD][hapmap];0.90[JPT][hapmap];0.80[ASN][1000 genomes]
rs8004339	0.81[EUR][1000 genomes]
rs8005022	0.91[CEU][hapmap];0.83[GIH][hapmap];0.81[EUR][1000 genomes]
rs8008894	0.86[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs8008912	0.93[EUR][1000 genomes]
rs8009178	0.91[CEU][hapmap];0.86[EUR][1000 genomes]
rs8011174	0.81[CEU][hapmap]
rs8011715	0.95[CEU][hapmap];0.84[GIH][hapmap];0.97[TSI][hapmap];0.96[EUR][1000 genomes]
rs8014426	0.86[EUR][1000 genomes]
rs8014914	0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs8015845	1.00[CHB][hapmap];1.00[CHD][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.92[TSI][hapmap];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8016428	0.85[EUR][1000 genomes]
rs8016558	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs8016567	0.86[CHB][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs8017060	0.82[EUR][1000 genomes]
rs8022248	0.85[EUR][1000 genomes]
rs9919903	0.98[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	nsv534288	chr14:37254539-37697745	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	17 gene(s)	inside rSNPs	diseases
2	nsv1036201	chr14:37498841-37542041	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv1037719	chr14:37498841-37546359	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv526786	chr14:37499904-37537352	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv1048854	chr14:37505438-37546359	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs7149154	PPP2R3C	cis	cerebellum	SCAN

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:37514800-37516800	Enhancers	HUVEC	blood vessel
2	chr14:37515200-37517800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr14:37515400-37518200	Enhancers	Stomach Mucosa	stomach
4	chr14:37515600-37518400	Weak transcription	Pancreas	Pancrea
5	chr14:37516000-37518800	Enhancers	Muscle Satellite Cultured Cells	--
6	chr14:37516200-37516800	Bivalent Enhancer	HepG2	liver
7	chr14:37516200-37517800	Enhancers	NHEK	skin
8	chr14:37516200-37518800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr14:37516400-37517000	Weak transcription	HSMMtube	muscle
10	chr14:37516400-37518600	Enhancers	HMEC	breast
11	chr14:37516600-37516800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr14:37516600-37517000	Enhancers	K562	blood
13	chr14:37516600-37517600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr14:37516600-37518000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr14:37516600-37518600	Enhancers	NH-A	brain

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