Variant report

Variant	rs2399367
Chromosome Location	chr3:110641021-110641022
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	chr3:110640909..110643004-chr3:110644318..110646224,2	MCF-7	breast:

Extended variants
information (count: 77 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:71)

rs_ID	r²[population]
rs10049325	0.88[ASN][1000 genomes]
rs10511290	0.88[ASN][1000 genomes]
rs1075303	0.89[ASN][1000 genomes]
rs11927478	0.86[ASN][1000 genomes]
rs12493974	0.88[AFR][1000 genomes]
rs13080214	0.86[ASN][1000 genomes]
rs13093547	0.86[ASN][1000 genomes]
rs1350980	1.00[ASN][1000 genomes]
rs1381828	0.89[ASN][1000 genomes]
rs1381836	0.83[AFR][1000 genomes]
rs1462325	0.87[ASN][1000 genomes]
rs1462789	0.86[ASN][1000 genomes]
rs1462790	0.89[ASN][1000 genomes]
rs1462793	0.96[ASN][1000 genomes]
rs1462795	0.89[ASN][1000 genomes]
rs1462798	0.88[AFR][1000 genomes]
rs1462801	0.88[ASN][1000 genomes]
rs1462807	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1564056	0.88[ASN][1000 genomes]
rs1580288	0.89[ASN][1000 genomes]
rs1585594	0.95[ASN][1000 genomes]
rs1585595	0.88[ASN][1000 genomes]
rs1599663	0.95[ASN][1000 genomes]
rs1599664	0.95[ASN][1000 genomes]
rs16857483	0.89[ASN][1000 genomes]
rs1824666	0.95[ASN][1000 genomes]
rs1903755	0.92[ASN][1000 genomes]
rs1903759	0.94[ASN][1000 genomes]
rs1993802	0.88[ASN][1000 genomes]
rs1993803	0.88[ASN][1000 genomes]
rs2002969	0.89[ASN][1000 genomes]
rs2100875	0.95[ASN][1000 genomes]
rs2219706	0.88[AFR][1000 genomes]
rs2399368	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2399369	0.83[AFR][1000 genomes]
rs2399370	0.94[ASN][1000 genomes]
rs2399371	0.90[ASN][1000 genomes]
rs2399378	0.89[ASN][1000 genomes]
rs2895376	0.87[ASN][1000 genomes]
rs35665971	0.89[ASN][1000 genomes]
rs4102676	0.89[ASN][1000 genomes]
rs4234401	1.00[ASN][1000 genomes]
rs4682028	0.96[ASN][1000 genomes]
rs4682212	0.88[ASN][1000 genomes]
rs4682215	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs5000277	0.89[ASN][1000 genomes]
rs6437934	0.89[AFR][1000 genomes]
rs6437940	0.86[ASN][1000 genomes]
rs66513024	0.89[ASN][1000 genomes]
rs67056469	0.89[ASN][1000 genomes]
rs67832786	0.95[ASN][1000 genomes]
rs6787921	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6805399	0.96[ASN][1000 genomes]
rs6805467	0.91[AFR][1000 genomes]
rs6808847	0.94[ASN][1000 genomes]
rs71618767	0.83[ASN][1000 genomes]
rs723023	0.90[ASN][1000 genomes]
rs723025	0.89[ASN][1000 genomes]
rs7622983	0.89[ASN][1000 genomes]
rs7623003	0.88[ASN][1000 genomes]
rs7623064	0.89[ASN][1000 genomes]
rs7623103	0.89[ASN][1000 genomes]
rs7637068	0.89[ASN][1000 genomes]
rs7644948	0.89[ASN][1000 genomes]
rs969940	0.83[AFR][1000 genomes]
rs9817950	0.86[ASN][1000 genomes]
rs9826064	0.89[ASN][1000 genomes]
rs9839299	0.96[ASN][1000 genomes]
rs9839674	0.89[ASN][1000 genomes]
rs9874206	0.88[ASN][1000 genomes]
rs9876543	0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1003106	chr3:110264476-111105943	Weak transcription Enhancers Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv1014199	chr3:110293896-110754155	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	esv2762345	chr3:110614389-110668843	Enhancers ZNF genes & repeats Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv829674	chr3:110616256-110771049	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv460821	chr3:110637471-111501097	Enhancers Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Weak transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
6	nsv591275	chr3:110637471-111501097	Strong transcription Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:110620200-110653800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr3:110637200-110646000	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr3:110638600-110642000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
4	chr3:110639800-110641800	Weak transcription	H1 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links