Variant report

Variant	rs868767
Chromosome Location	chr3:141377330-141377331
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:141376839..141379290-chr3:141593720..141595646,2	MCF-7	breast:
2	chr3:141377266..141379551-chr3:141385595..141387849,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000069849	Chromatin interaction

Extended variants
information (count: 52 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs10935431	0.81[JPT][hapmap]
rs12632759	0.94[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs13088397	0.87[ASN][1000 genomes]
rs13089727	0.81[JPT][hapmap]
rs1400685	0.83[CHD][hapmap];0.95[JPT][hapmap];0.85[ASN][1000 genomes]
rs1532247	0.85[ASN][1000 genomes]
rs1994845	0.95[JPT][hapmap];0.86[ASN][1000 genomes]
rs2018495	0.81[AMR][1000 genomes]
rs2030186	0.89[ASN][1000 genomes]
rs2030187	0.82[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs2640001	0.83[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs2640019	0.95[JPT][hapmap];0.90[ASN][1000 genomes]
rs295294	0.95[JPT][hapmap];0.83[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs295296	0.95[JPT][hapmap];0.81[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs295314	0.85[ASN][1000 genomes]
rs295315	0.97[CHD][hapmap];0.95[JPT][hapmap];0.83[MEX][hapmap];0.85[ASN][1000 genomes]
rs295317	0.90[JPT][hapmap];0.87[ASN][1000 genomes]
rs34319548	0.82[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs34867571	0.90[ASN][1000 genomes]
rs4467426	0.95[JPT][hapmap];0.86[ASN][1000 genomes]
rs4634089	0.90[ASN][1000 genomes]
rs4683407	0.95[JPT][hapmap];0.86[ASN][1000 genomes]
rs4683615	0.86[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs4683616	0.86[ASN][1000 genomes]
rs59312699	0.83[ASN][1000 genomes]
rs6440024	0.83[CHD][hapmap];0.95[JPT][hapmap];0.86[ASN][1000 genomes]
rs6440025	0.86[ASN][1000 genomes]
rs6768509	0.81[JPT][hapmap]
rs6774986	0.86[ASN][1000 genomes]
rs6784270	0.95[JPT][hapmap]
rs6784413	0.95[JPT][hapmap];0.86[ASN][1000 genomes]
rs6784623	0.86[ASN][1000 genomes]
rs6791890	0.83[CHD][hapmap];0.95[JPT][hapmap];0.87[ASN][1000 genomes]
rs6805124	0.95[JPT][hapmap];0.86[ASN][1000 genomes]
rs72996335	0.81[AMR][1000 genomes]
rs7618625	0.83[CHD][hapmap];0.95[JPT][hapmap];0.86[ASN][1000 genomes]
rs7627285	0.86[ASN][1000 genomes]
rs7639695	0.95[JPT][hapmap];0.85[ASN][1000 genomes]
rs7642620	0.86[ASN][1000 genomes]
rs7650428	0.82[ASN][1000 genomes]
rs7650897	0.81[JPT][hapmap]
rs7653258	0.84[ASN][1000 genomes]
rs868768	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9289635	0.86[ASN][1000 genomes]
rs9289636	0.86[ASN][1000 genomes]
rs9289637	0.86[ASN][1000 genomes]
rs9812758	0.84[ASN][1000 genomes]
rs9841650	0.87[ASN][1000 genomes]
rs9841805	0.86[ASN][1000 genomes]
rs9861838	0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949709	chr3:141295050-142178144	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
2	nsv524429	chr3:141372391-141377330	Active TSS Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:141364400-141377600	Weak transcription	Aorta	Aorta
2	chr3:141376200-141378200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr3:141376400-141377600	Enhancers	Breast Myoepithelial Primary Cells	Breast
4	chr3:141376400-141377600	Flanking Active TSS	Colon Smooth Muscle	Colon
5	chr3:141377000-141377800	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
6	chr3:141377000-141378400	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
7	chr3:141377200-141377400	Enhancers	Placenta	Placenta
8	chr3:141377200-141377600	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr3:141377200-141377600	Flanking Active TSS	Rectal Smooth Muscle	rectum
10	chr3:141377200-141377800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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