Variant report

Variant	rs3741132
Chromosome Location	chr11:73978243-73978244
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	chr11:73972820..73975528-chr11:73978164..73980446,3	K562	blood:
2	chr11:73971856..73973476-chr11:73977931..73979891,2	MCF-7	breast:

Extended variants
information (count: 64 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:59)

rs_ID	r²[population]
rs10431176	0.83[CEU][hapmap];0.87[CHD][hapmap]
rs10459047	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10898957	0.87[CHD][hapmap]
rs10898962	0.83[CEU][hapmap];0.87[CHD][hapmap]
rs10898966	0.83[CEU][hapmap];0.85[CHD][hapmap]
rs10898973	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10898974	0.92[CEU][hapmap];1.00[CHB][hapmap];0.88[JPT][hapmap];0.95[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10898975	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.88[JPT][hapmap];1.00[MEX][hapmap];0.83[TSI][hapmap];0.95[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10898976	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];0.92[GIH][hapmap];0.94[JPT][hapmap];0.91[MEX][hapmap];0.81[TSI][hapmap];0.95[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10898980	1.00[CEU][hapmap];0.85[CHD][hapmap];0.84[GIH][hapmap];0.90[MEX][hapmap];0.83[TSI][hapmap]
rs11235994	0.84[CHD][hapmap]
rs11235995	0.87[CHD][hapmap]
rs11236000	0.87[CHD][hapmap]
rs11236029	0.83[CEU][hapmap];0.87[CHD][hapmap]
rs11236042	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.88[JPT][hapmap];1.00[MEX][hapmap];0.83[TSI][hapmap];0.95[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11236043	1.00[CEU][hapmap];1.00[CHB][hapmap];0.88[JPT][hapmap];0.95[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11236044	0.95[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11236052	1.00[CEU][hapmap];0.90[CHB][hapmap];0.80[JPT][hapmap];0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11236053	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[CHD][hapmap];0.92[GIH][hapmap];0.82[JPT][hapmap];0.90[MEX][hapmap];0.83[TSI][hapmap];0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11236054	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11236055	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs11236060	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11236063	1.00[CEU][hapmap];0.81[EUR][1000 genomes]
rs11236071	1.00[CEU][hapmap];0.85[CHD][hapmap];0.88[GIH][hapmap];0.90[MEX][hapmap];0.83[TSI][hapmap]
rs11236077	1.00[CEU][hapmap];0.88[GIH][hapmap];0.90[MEX][hapmap]
rs11236092	1.00[CEU][hapmap];0.81[GIH][hapmap]
rs11600314	0.87[CHD][hapmap]
rs11602451	0.87[CHD][hapmap]
rs11604713	0.87[CHD][hapmap]
rs11608147	0.87[CHD][hapmap]
rs12049823	0.85[CEU][hapmap]
rs12223320	0.87[CHD][hapmap]
rs12225446	1.00[CEU][hapmap];1.00[CHB][hapmap];0.80[JPT][hapmap];0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12574038	0.87[CHD][hapmap]
rs12574047	0.87[CHD][hapmap]
rs17132964	1.00[CEU][hapmap];0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs1944971	0.83[CEU][hapmap];0.87[CHD][hapmap]
rs2178000	0.87[CHD][hapmap]
rs2282488	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.87[JPT][hapmap];0.91[MEX][hapmap];0.83[TSI][hapmap];0.95[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs3741133	0.83[CEU][hapmap];0.87[CHD][hapmap]
rs3819114	0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs3888908	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs3894652	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4121668	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs515924	0.85[CEU][hapmap]
rs550552	0.92[CEU][hapmap]
rs58852370	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs588725	0.85[CEU][hapmap]
rs61902380	0.83[EUR][1000 genomes]
rs625532	0.91[CEU][hapmap]
rs630078	0.92[CEU][hapmap]
rs639228	0.92[CEU][hapmap]
rs658976	0.92[CEU][hapmap]
rs676103	0.85[CEU][hapmap]
rs7110734	0.87[CHD][hapmap]
rs7117465	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.89[GIH][hapmap];1.00[JPT][hapmap];0.82[MEX][hapmap];0.97[ASN][1000 genomes]
rs7125032	0.87[CHD][hapmap]
rs7949639	0.83[CEU][hapmap];0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7951617	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.88[JPT][hapmap];0.83[TSI][hapmap];0.95[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][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	esv2757451	chr11:73842609-74545888	Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Enhancers Genic enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
2	esv2759837	chr11:73842609-74557597	Flanking Active TSS Enhancers Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
3	esv34979	chr11:73878688-74533452	Enhancers Weak transcription Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	85 gene(s)	inside rSNPs	diseases
4	esv2758277	chr11:73887567-74557597	Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	85 gene(s)	inside rSNPs	diseases
5	nsv825994	chr11:73936667-74534455	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers 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	83 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs3741132	PPME1	cis	cerebellum	SCAN
rs3741132	STARD10	cis	parietal	SCAN
rs3741132	P4HA3	cis	cerebellum	SCAN

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:73966200-73980000	Weak transcription	Gastric	stomach
2	chr11:73966400-73979200	Weak transcription	Primary T cells from cord blood	blood
3	chr11:73968000-73979000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr11:73969400-73987600	Weak transcription	NH-A	brain
5	chr11:73969800-73980400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr11:73970000-73980000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr11:73970000-73987600	Weak transcription	Muscle Satellite Cultured Cells	--
8	chr11:73975400-73980800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr11:73975800-73979400	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr11:73976600-73978800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr11:73976600-73980000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr11:73976600-73983200	Weak transcription	HSMM	muscle
13	chr11:73976800-73979800	Weak transcription	Osteobl	bone
14	chr11:73977000-73979600	Weak transcription	Placenta	Placenta
15	chr11:73977200-73979200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr11:73977800-73978400	Enhancers	Fetal Muscle Leg	muscle
17	chr11:73978000-73979200	Enhancers	Hela-S3	cervix
18	chr11:73978000-73980000	Genic enhancers	A549	lung
19	chr11:73978200-73979400	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr11:73978200-73982000	Enhancers	Fetal Thymus	thymus

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links