Variant report

Variant	rs6913941
Chromosome Location	chr6:35163735-35163736
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:35139023..35142448-chr6:35162991..35165848,3	MCF-7	breast:
2	chr6:35118710..35120443-chr6:35162484..35164592,2	MCF-7	breast:
3	chr6:35146928..35151829-chr6:35162484..35168348,5	K562	blood:
4	chr6:34761569..34764046-chr6:35162032..35164160,2	K562	blood:
5	chr6:35147057..35148601-chr6:35163604..35165162,2	MCF-7	breast:
6	chr6:35148681..35155694-chr6:35156262..35164857,12	MCF-7	breast:
7	chr6:35132639..35135102-chr6:35162466..35164751,2	MCF-7	breast:

Extended variants
information (count: 96 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:95)

rs_ID	r²[population]
rs10080361	0.89[ASN][1000 genomes]
rs1013907	0.91[AFR][1000 genomes];0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10807150	0.81[ASN][1000 genomes]
rs10947540	0.90[ASN][1000 genomes]
rs1108709	0.82[ASN][1000 genomes]
rs1194	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs13214290	0.92[ASN][1000 genomes]
rs1557567	0.81[ASN][1000 genomes]
rs1557568	0.81[ASN][1000 genomes]
rs1590381	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1888822	0.82[ASN][1000 genomes]
rs1888823	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1888824	0.90[ASN][1000 genomes]
rs1888825	0.90[ASN][1000 genomes]
rs1894650	0.90[ASN][1000 genomes]
rs1894651	0.89[ASN][1000 genomes]
rs1894652	0.86[ASN][1000 genomes]
rs1894653	0.86[ASN][1000 genomes]
rs1929847	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1929849	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1987673	0.82[ASN][1000 genomes]
rs2006184	0.86[ASN][1000 genomes]
rs2018373	0.83[ASN][1000 genomes]
rs2071920	0.81[ASN][1000 genomes]
rs2183834	0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2267658	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2267660	0.86[ASN][1000 genomes]
rs2267661	0.86[ASN][1000 genomes]
rs2267662	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2267663	0.90[ASN][1000 genomes]
rs2284195	0.90[ASN][1000 genomes]
rs2395614	0.82[ASN][1000 genomes]
rs3798342	0.86[ASN][1000 genomes]
rs3800382	0.86[ASN][1000 genomes]
rs3800383	0.88[ASN][1000 genomes]
rs3800385	0.92[ASN][1000 genomes]
rs3800386	0.88[ASN][1000 genomes]
rs3800387	0.88[ASN][1000 genomes]
rs3800388	0.88[ASN][1000 genomes]
rs3800392	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs3800393	0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs3800396	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3800398	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3800399	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3800401	0.90[ASN][1000 genomes]
rs4711409	0.91[AFR][1000 genomes];0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4711411	0.90[ASN][1000 genomes]
rs4711413	0.86[ASN][1000 genomes]
rs4711414	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4713841	0.80[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs4713845	0.90[ASN][1000 genomes]
rs4713848	0.84[ASN][1000 genomes]
rs58925593	0.86[ASN][1000 genomes]
rs62403575	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6457812	0.81[ASN][1000 genomes]
rs68164647	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6902523	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6907324	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6907573	0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6907795	0.81[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6913037	0.90[ASN][1000 genomes]
rs6916364	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6920747	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6927730	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6928769	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6938946	0.87[ASN][1000 genomes]
rs6940375	0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs72909061	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7763946	0.92[ASN][1000 genomes]
rs7769906	0.90[ASN][1000 genomes]
rs7772212	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs8205	0.81[ASN][1000 genomes]
rs914547	0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9296144	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9348970	0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9366882	0.81[ASN][1000 genomes]
rs9366883	0.90[ASN][1000 genomes]
rs9368854	0.88[ASN][1000 genomes]
rs9368857	0.86[ASN][1000 genomes]
rs9380497	0.90[ASN][1000 genomes]
rs9380498	0.80[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9380501	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9380502	0.81[ASN][1000 genomes]
rs9394283	0.92[ASN][1000 genomes]
rs9394289	0.90[ASN][1000 genomes]
rs9469958	0.88[ASN][1000 genomes]
rs9469964	0.92[ASN][1000 genomes]
rs9469972	0.81[ASN][1000 genomes]
rs9469975	0.80[ASN][1000 genomes]
rs9469979	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9469982	0.81[ASN][1000 genomes]
rs965272	0.81[ASN][1000 genomes]
rs968828	0.82[ASN][1000 genomes]
rs975496	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs991145	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3428128	chr6:35150524-35225843	Bivalent Enhancer Enhancers Genic enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:35154000-35169800	Weak transcription	Right Atrium	heart
2	chr6:35154400-35169200	Weak transcription	Fetal Heart	heart
3	chr6:35158600-35167200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr6:35159400-35164800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr6:35160400-35164800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr6:35160800-35163800	Enhancers	K562	blood
7	chr6:35161000-35167800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr6:35161400-35164800	Weak transcription	HMEC	breast
9	chr6:35161600-35167800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr6:35161600-35169400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr6:35161600-35170000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr6:35162000-35164800	Enhancers	Osteobl	bone
13	chr6:35163000-35164800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr6:35163200-35164000	Weak transcription	Muscle Satellite Cultured Cells	--
15	chr6:35163200-35171200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr6:35163400-35164800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr6:35163600-35165400	Weak transcription	HepG2	liver
18	chr6:35163600-35167200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr6:35163600-35171000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin

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