Variant report

Variant	rs4664541
Chromosome Location	chr2:153036935-153036936
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:33)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:33 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:41380246..41381942-chr2:153036711..153038211,2	MCF-7	breast:
2	chr2:153031745..153033920-chr2:153034971..153037430,3	MCF-7	breast:
3	chr11:65381999..65382539-chr2:153036731..153037231,2	Hela-S3	cervix:
4	chr2:153036711..153037231-chr3:73159944..73160630,4	HCT-116	colon:
5	chr17:41464183..41467827-chr2:153035211..153038231,8	K562	blood:
6	chr13:90583696..90585208-chr2:153036711..153038231,2	MCF-7	breast:
7	chr17:41464180..41467827-chr2:153035231..153038231,5	K562	blood:
8	chr17:41466181..41466829-chr2:153036711..153037211,2	NB4	blood:
9	chr17:41380499..41383397-chr2:153035231..153038231,3	K562	blood:
10	chr11:62608620..62609153-chr2:153036711..153037231,6	MCF-7	breast:
11	chr2:153030695..153035582-chr2:153035899..153041434,6	MCF-7	breast:
12	chr11:62608617..62609197-chr2:153036711..153037231,6	MCF-7	breast:
13	chr11:62608622..62609130-chr2:153036711..153037211,2	NB4	blood:
14	chr2:153036711..153037231-chr7:10882214..10882734,2	Hela-S3	cervix:
15	chr2:153035231..153038231-chr3:73159887..73161626,5	K562	blood:
16	chr10:103124111..103124628-chr2:153036711..153037231,2	MCF-7	breast:
17	chr11:62608617..62609637-chr2:153036711..153037231,7	HCT-116	colon:
18	chr1:160080985..160082488-chr2:153036731..153038231,2	MCF-7	breast:
19	chr17:41398980..41402235-chr2:153035211..153038231,7	K562	blood:
20	chr2:153036711..153038231-chr3:73158624..73161630,6	MCF-7	breast:
21	chr11:62608623..62609126-chr2:153036711..153037211,2	Hela-S3	cervix:
22	chr11:62607620..62609197-chr2:153035231..153038211,4	MCF-7	breast:
23	chr17:41465202..41465887-chr2:153036731..153037231,2	Hela-S3	cervix:
24	chr11:62607625..62609221-chr2:153036711..153038231,6	K562	blood:
25	chr17:41463098..41465894-chr2:153036711..153038231,3	MCF-7	breast:
26	chr2:153035211..153038231-chr3:73158573..73161626,5	K562	blood:
27	chr17:41465181..41465686-chr2:153036711..153037211,2	HCT-116	colon:
28	chr17:41381897..41383499-chr2:153035231..153038211,3	K562	blood:
29	chr2:153036211..153037211-chr3:73159960..73160604,5	Hela-S3	cervix:
30	chr11:62607630..62609221-chr2:153036711..153038231,4	K562	blood:
31	chr17:41399135..41402235-chr2:153035211..153038231,6	K562	blood:
32	chr2:153036711..153037231-chr2:174786141..174786661,3	Hela-S3	cervix:
33	chr17:41277445..41279524-chr2:153036711..153038231,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000115145	Chromatin interaction
ENSG00000198496	Chromatin interaction
ENSG00000236383	Chromatin interaction
ENSG00000012048	Chromatin interaction
ENSG00000133316	Chromatin interaction
ENSG00000223247	Chromatin interaction
ENSG00000188825	Chromatin interaction

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs10194916	0.81[AMR][1000 genomes]
rs10497098	0.92[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10931006	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11685937	0.86[EUR][1000 genomes]
rs11883562	0.92[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11898205	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12474885	0.92[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12479199	0.92[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12623266	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12693288	0.92[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12693289	0.92[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12693290	0.92[AFR][1000 genomes];0.89[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12994907	0.85[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs16823676	0.92[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1806557	0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1986711	0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2345899	0.89[AFR][1000 genomes];0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2881244	0.92[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4560063	0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4581846	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4664087	0.83[AMR][1000 genomes]
rs4664088	0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6433939	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6706684	0.92[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6710166	0.92[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6713219	0.92[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6756620	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7355335	0.93[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7579212	0.84[AFR][1000 genomes];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1005746	chr2:152361972-153059840	Strong transcription Weak transcription Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
2	nsv535984	chr2:152361972-153059840	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
3	nsv875287	chr2:152714680-153110573	Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Bivalent/Poised TSS Flanking Active 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 target site	20 gene(s)	inside rSNPs	diseases
4	nsv875288	chr2:152716628-153183646	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
5	nsv875289	chr2:152720030-153183646	Enhancers Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Strong transcription Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
6	esv1847028	chr2:152863856-153045036	Weak transcription Active TSS Bivalent/Poised TSS Strong transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
7	nsv1004308	chr2:152980087-153154534	Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
8	nsv535985	chr2:152980087-153154534	Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
9	nsv459740	chr2:152986041-153045036	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
10	nsv583316	chr2:152986041-153045036	Bivalent/Poised TSS ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
11	esv3693434	chr2:152998467-153208713	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:153033200-153037200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links