Variant report

Variant	rs9822705
Chromosome Location	chr3:161079146-161079147
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:161041894..161044446-chr3:161076689..161079941,3	MCF-7	breast:
2	chr3:160936365..160960187-chr3:161078472..161094658,51	MCF-7	breast:

Variant related genes	Relation type
ENSG00000271052	Chromatin interaction
ENSG00000169251	Chromatin interaction
ENSG00000240138	Chromatin interaction

Extended variants
information (count: 104 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:100)

rs_ID	r²[population]
rs1017799	1.00[CHB][hapmap];0.89[JPT][hapmap];0.91[YRI][hapmap];0.87[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12486998	0.85[AMR][1000 genomes]
rs12487002	0.85[AMR][1000 genomes]
rs12488127	0.85[AMR][1000 genomes]
rs12489004	1.00[CHB][hapmap];0.80[AFR][1000 genomes];0.88[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs12489125	0.81[ASN][1000 genomes]
rs12490149	1.00[CHB][hapmap];0.88[JPT][hapmap];0.93[ASN][1000 genomes]
rs12491623	0.85[AMR][1000 genomes]
rs12494520	0.82[AMR][1000 genomes]
rs12496235	0.85[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs13315320	0.88[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs13319558	1.00[CHB][hapmap];0.89[JPT][hapmap];0.94[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs13319771	1.00[CHB][hapmap];0.86[JPT][hapmap];0.81[YRI][hapmap];0.88[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs1450518	0.82[AMR][1000 genomes]
rs16831942	0.81[ASN][1000 genomes]
rs2035499	0.85[AMR][1000 genomes]
rs2306209	1.00[CHB][hapmap];0.88[JPT][hapmap];0.95[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs28451189	0.88[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs28704960	0.81[ASN][1000 genomes]
rs28713364	0.85[AMR][1000 genomes]
rs4296611	0.88[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs4352387	1.00[CHB][hapmap];0.88[JPT][hapmap];0.88[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs4468992	1.00[CHB][hapmap];0.89[JPT][hapmap];0.88[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs4580574	0.88[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs4635725	0.88[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs57903480	0.86[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs58851337	0.85[AMR][1000 genomes]
rs58892449	0.82[AMR][1000 genomes]
rs59368066	0.85[AMR][1000 genomes]
rs59567999	0.88[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs59757775	0.83[ASN][1000 genomes]
rs60121330	0.81[ASN][1000 genomes]
rs6441363	0.82[AMR][1000 genomes]
rs6441365	0.88[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs6441372	0.83[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs6441375	1.00[CHB][hapmap];0.88[JPT][hapmap];0.91[YRI][hapmap];0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6762064	0.88[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs6774919	0.88[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs6775446	1.00[CHB][hapmap];0.88[JPT][hapmap];0.82[YRI][hapmap];0.80[AFR][1000 genomes];0.88[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs6775931	1.00[CHB][hapmap];0.88[JPT][hapmap];0.88[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs6778186	0.94[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs6781086	0.91[AMR][1000 genomes]
rs6782415	1.00[CHB][hapmap];0.88[JPT][hapmap];0.88[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs6782518	1.00[CHB][hapmap];0.88[JPT][hapmap];0.88[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs6785714	1.00[CHB][hapmap];0.84[JPT][hapmap];0.82[YRI][hapmap];0.82[AFR][1000 genomes];0.88[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs6787447	0.82[AFR][1000 genomes];0.88[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs6787697	0.86[AMR][1000 genomes]
rs6788738	0.85[AMR][1000 genomes]
rs6790805	0.85[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs6793980	0.88[AMR][1000 genomes]
rs6801664	0.88[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs6805976	0.88[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs73017340	0.94[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs73026933	0.81[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs73026967	0.88[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs73026968	0.88[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs73026983	0.80[AFR][1000 genomes];0.88[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs73026987	0.88[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs73026989	0.88[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs73878309	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73878323	0.85[AMR][1000 genomes]
rs73878329	0.85[AMR][1000 genomes]
rs7614130	0.85[AMR][1000 genomes]
rs7615833	1.00[CHB][hapmap];0.88[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs7615868	0.85[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs7624791	0.94[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs7626773	1.00[CHB][hapmap];0.89[JPT][hapmap];0.94[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs7629841	0.85[AMR][1000 genomes]
rs7634299	1.00[CHB][hapmap];0.89[JPT][hapmap];0.88[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs7651924	1.00[CHB][hapmap];0.89[JPT][hapmap];0.91[YRI][hapmap];0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7652624	1.00[CHB][hapmap];0.81[JPT][hapmap];0.80[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs9290070	0.88[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs9290071	0.88[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs9812574	0.90[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9818470	0.83[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs9819793	1.00[CHB][hapmap];0.86[JPT][hapmap];0.88[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs9822916	1.00[CHB][hapmap];0.88[JPT][hapmap];0.82[YRI][hapmap];0.82[AFR][1000 genomes];0.88[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs9824535	0.81[ASN][1000 genomes]
rs9824805	1.00[CHB][hapmap];0.89[JPT][hapmap];0.82[YRI][hapmap];0.80[AFR][1000 genomes];0.88[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs9830183	0.85[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs9833270	0.90[ASN][1000 genomes]
rs9834806	0.82[AMR][1000 genomes]
rs9835530	1.00[CHB][hapmap];0.89[JPT][hapmap];0.91[YRI][hapmap];0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9838945	0.80[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs9841871	0.88[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs9842290	0.80[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs9847842	1.00[CHB][hapmap];0.88[JPT][hapmap];0.88[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs9851699	0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9855112	0.85[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs9855572	0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9856742	0.88[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs9859641	1.00[CHB][hapmap];0.88[JPT][hapmap];0.82[YRI][hapmap];0.82[AFR][1000 genomes];0.88[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs9860980	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9862867	1.00[CHB][hapmap];0.89[JPT][hapmap];0.94[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs9871753	0.88[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs9876077	0.94[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs9877309	1.00[CHB][hapmap];0.86[JPT][hapmap];0.88[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs9880536	1.00[CHB][hapmap];0.89[JPT][hapmap];0.82[YRI][hapmap];0.83[AFR][1000 genomes];0.94[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs9884100	0.88[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs9985364	0.88[AMR][1000 genomes];0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv931072	chr3:160669567-161159779	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	98 gene(s)	inside rSNPs	diseases
2	nsv533237	chr3:161019834-161804660	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	91 gene(s)	inside rSNPs	diseases
3	nsv829772	chr3:161047817-161202554	Bivalent Enhancer Bivalent/Poised TSS Enhancers Flanking Active TSS Strong transcription Weak transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	88 gene(s)	inside rSNPs	diseases
4	nsv963570	chr3:161076656-161088849	Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription	Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:161059800-161089200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr3:161064400-161083000	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr3:161068200-161083200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr3:161068400-161083200	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr3:161076200-161083200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr3:161077800-161079800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
7	chr3:161079000-161081800	Enhancers	Pancreatic Islets	Pancreatic Islet

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links