Variant report

Variant	rs841925
Chromosome Location	chr5:101627776-101627777
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:101626744..101629663-chr5:101630622..101633299,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000173930	Chromatin interaction

Extended variants
information (count: 76 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:68)

rs_ID	r²[population]
rs10051525	0.81[AFR][1000 genomes];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10057529	0.91[ASN][1000 genomes]
rs10057599	0.91[ASN][1000 genomes]
rs10069466	0.81[AFR][1000 genomes];0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10073052	0.91[ASN][1000 genomes]
rs10479191	0.91[ASN][1000 genomes]
rs1078338	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1117130	0.81[ASN][1000 genomes]
rs1452057	0.81[ASN][1000 genomes]
rs1452059	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1452060	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1452065	0.86[ASN][1000 genomes]
rs1823694	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1875634	0.84[AFR][1000 genomes]
rs2004550	0.91[ASN][1000 genomes]
rs2004551	0.91[ASN][1000 genomes]
rs2010590	0.91[ASN][1000 genomes]
rs2060836	0.81[ASN][1000 genomes]
rs2060837	0.81[ASN][1000 genomes]
rs2167586	0.88[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs2548725	0.83[AFR][1000 genomes];0.91[AMR][1000 genomes];0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2600826	0.88[AFR][1000 genomes];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2600831	0.89[AFR][1000 genomes];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs28532891	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2895806	0.91[ASN][1000 genomes]
rs3096214	0.87[AFR][1000 genomes];0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs3114660	0.91[ASN][1000 genomes]
rs3114661	0.84[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3114665	0.89[AFR][1000 genomes];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs384615	0.81[AFR][1000 genomes];0.90[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs386464	0.86[AFR][1000 genomes];0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs404598	0.82[AFR][1000 genomes];0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs416332	0.80[EUR][1000 genomes]
rs4343814	0.91[ASN][1000 genomes]
rs56358831	0.81[ASN][1000 genomes]
rs56881277	0.91[ASN][1000 genomes]
rs62372208	0.91[ASN][1000 genomes]
rs62372209	0.91[ASN][1000 genomes]
rs62372210	0.91[ASN][1000 genomes]
rs6860720	0.81[ASN][1000 genomes]
rs6866255	0.85[AFR][1000 genomes]
rs6878190	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6878326	0.81[ASN][1000 genomes]
rs6881331	0.91[ASN][1000 genomes]
rs6882313	0.91[ASN][1000 genomes]
rs6884162	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6893391	0.81[ASN][1000 genomes]
rs6893723	0.87[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs6895407	0.91[ASN][1000 genomes]
rs709369	0.89[ASN][1000 genomes]
rs709371	0.91[ASN][1000 genomes]
rs709372	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7701832	0.91[ASN][1000 genomes]
rs7702418	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7721548	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7722680	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7734926	0.98[AFR][1000 genomes];0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs841921	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs841923	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs841924	0.90[ASN][1000 genomes]
rs841927	0.91[ASN][1000 genomes]
rs841928	0.91[ASN][1000 genomes]
rs841929	0.91[ASN][1000 genomes]
rs841930	0.91[ASN][1000 genomes]
rs841931	0.91[ASN][1000 genomes]
rs841933	0.86[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs896544	0.91[ASN][1000 genomes]
rs896545	0.91[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1022551	chr5:101366177-101649643	Active TSS Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv882505	chr5:101397849-101652251	Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent Enhancer Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv1028787	chr5:101432086-101718569	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv817537	chr5:101489151-101992104	Active TSS Flanking Active TSS Weak transcription Enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
5	nsv1016176	chr5:101534391-102333606	Active TSS Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
6	nsv537831	chr5:101534391-102333606	Genic enhancers Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
7	nsv522882	chr5:101596633-101782930	Enhancers Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
8	nsv1029894	chr5:101620079-102516827	Enhancers Strong transcription Flanking Active TSS Weak transcription Bivalent Enhancer Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:101613400-101629400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr5:101619200-101630800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
3	chr5:101620600-101630600	Weak transcription	GM12878-XiMat	blood
4	chr5:101622800-101630200	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr5:101624400-101631400	Weak transcription	Pancreas	Pancrea
6	chr5:101625200-101629000	Weak transcription	HUES64 Cell Line	embryonic stem cell
7	chr5:101625400-101630600	Weak transcription	Liver	Liver
8	chr5:101626000-101630000	Weak transcription	Fetal Intestine Small	intestine
9	chr5:101626200-101629000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
10	chr5:101626200-101629400	Weak transcription	Primary monocytes fromperipheralblood	blood
11	chr5:101627200-101628800	Weak transcription	Monocytes-CD14+_RO01746	blood
12	chr5:101627200-101630400	Weak transcription	HepG2	liver
13	chr5:101627400-101629400	Enhancers	Primary neutrophils fromperipheralblood	blood
14	chr5:101627400-101630200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
15	chr5:101627600-101628000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood

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