Variant report

Variant	rs6785465
Chromosome Location	chr3:28271232-28271233
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr3:28270292..28273085-chr3:28279670..28282869,3	MCF-7	breast:
2	chr3:28270683..28272455-chr3:28281452..28283015,2	MCF-7	breast:
3	chr11:77184165..77185067-chr3:28270408..28271332,2	MCF-7	breast:
4	chr3:28269228..28272109-chr3:28273817..28276497,2	K562	blood:
5	chr3:28267433..28273143-chr3:28280771..28285939,7	K562	blood:

Variant related genes	Relation type
ENSG00000149269	Chromatin interaction
ENSG00000187118	Chromatin interaction
ENSG00000268635	Chromatin interaction

Extended variants
information (count: 68 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:65)

rs_ID	r²[population]
rs10510606	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11129312	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11129313	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11129314	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11129317	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11708368	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11708635	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11717202	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11916111	0.91[AFR][1000 genomes]
rs11920536	0.83[AFR][1000 genomes]
rs11920615	0.91[AFR][1000 genomes]
rs11921526	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11923769	0.83[AFR][1000 genomes]
rs11926903	0.91[AFR][1000 genomes]
rs11927668	0.81[AFR][1000 genomes]
rs12107183	0.80[AFR][1000 genomes]
rs12107191	0.80[AFR][1000 genomes]
rs12485853	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12485858	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12497510	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13069777	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13073936	0.82[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs13074515	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13085236	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13085477	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13092179	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1606391	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17021232	0.91[AFR][1000 genomes]
rs17021238	0.91[AFR][1000 genomes]
rs34109684	0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs34692982	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35504778	0.90[EUR][1000 genomes]
rs35813951	0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4680746	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs55940261	0.90[AFR][1000 genomes]
rs56687471	0.91[AFR][1000 genomes]
rs57358658	0.91[AFR][1000 genomes]
rs58886943	0.91[AFR][1000 genomes]
rs60425255	0.87[AFR][1000 genomes]
rs61479857	0.91[AFR][1000 genomes]
rs61548543	0.85[AFR][1000 genomes]
rs61633201	0.83[AFR][1000 genomes]
rs6778650	0.90[AFR][1000 genomes]
rs6780084	0.80[AFR][1000 genomes]
rs6782956	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6791708	0.91[AFR][1000 genomes]
rs6792110	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6792215	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6795634	0.80[AFR][1000 genomes]
rs6797580	0.91[AFR][1000 genomes]
rs6798101	0.91[AFR][1000 genomes]
rs6798266	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6802491	0.91[AFR][1000 genomes]
rs6809163	0.90[AFR][1000 genomes]
rs6809917	0.91[AFR][1000 genomes]
rs73822327	0.91[AFR][1000 genomes]
rs73823423	0.91[AFR][1000 genomes]
rs73823425	0.91[AFR][1000 genomes]
rs73823426	0.90[AFR][1000 genomes]
rs73823432	0.91[AFR][1000 genomes]
rs73823433	0.91[AFR][1000 genomes]
rs73823434	0.91[AFR][1000 genomes]
rs7610729	0.91[AFR][1000 genomes]
rs7635045	0.89[AFR][1000 genomes]
rs7639138	0.91[AFR][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	esv3328565	chr3:27991169-28915035	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
2	nsv876648	chr3:28060456-28280965	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv876649	chr3:28126595-28718454	Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:28270000-28272000	Enhancers	HepG2	liver
2	chr3:28270000-28280800	Weak transcription	H9 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links