Variant report

Variant	rs4710043
Chromosome Location	chr6:166810626-166810627
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:166795175..166797069-chr6:166810191..166812486,2	K562	blood:

Variant related genes	Relation type
ENSG00000261420	Chromatin interaction
ENSG00000060762	Chromatin interaction

Extended variants
information (count: 57 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:54)

rs_ID	r²[population]
rs1546853	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1546854	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1546855	0.95[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1569459	0.80[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1569460	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1569461	0.90[EUR][1000 genomes]
rs1977049	0.80[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1977050	0.80[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1977051	0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1977052	0.96[EUR][1000 genomes]
rs1977053	0.94[EUR][1000 genomes]
rs1977054	0.95[EUR][1000 genomes]
rs1977056	0.85[EUR][1000 genomes]
rs1997661	0.85[ASN][1000 genomes]
rs2179177	0.90[EUR][1000 genomes]
rs2343591	0.90[EUR][1000 genomes]
rs3734605	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3757194	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3757195	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4305699	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6456078	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6456079	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6456081	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6902813	0.85[ASN][1000 genomes]
rs6905635	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6906844	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6912695	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6918091	0.81[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs6918135	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs735297	0.85[ASN][1000 genomes]
rs7449629	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7744743	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7752716	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9283865	0.80[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9295338	0.95[EUR][1000 genomes]
rs9295341	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9295342	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9295343	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9295344	0.95[EUR][1000 genomes]
rs9295345	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9348123	0.87[EUR][1000 genomes]
rs9348124	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9348125	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9348126	0.96[EUR][1000 genomes]
rs9355574	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9355575	0.89[EUR][1000 genomes]
rs9356482	0.96[EUR][1000 genomes]
rs9356483	0.95[EUR][1000 genomes]
rs9364845	0.90[EUR][1000 genomes]
rs9364846	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs9364847	0.80[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs9364848	0.80[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9366009	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9366010	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3490076	chr6:166727901-167306743	Strong transcription Weak transcription Flanking Active TSS Genic enhancers Enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	25 gene(s)	inside rSNPs	diseases
2	esv3490077	chr6:166727901-167306743	Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	25 gene(s)	inside rSNPs	diseases
3	nsv523548	chr6:166796433-166819774	Flanking Active TSS Weak transcription Active TSS Enhancers Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:166797600-166835800	Weak transcription	Right Atrium	heart
2	chr6:166798000-166812200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr6:166802400-166822400	Weak transcription	Gastric	stomach
4	chr6:166804200-166822200	Weak transcription	Brain Angular Gyrus	brain
5	chr6:166804800-166812200	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr6:166805800-166812800	Enhancers	HepG2	liver
7	chr6:166808200-166911800	Weak transcription	Psoas Muscle	Psoas
8	chr6:166809200-166814200	Weak transcription	Fetal Heart	heart
9	chr6:166809600-166812200	Weak transcription	Liver	Liver

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