Variant report

Variant	rs59151681
Chromosome Location	chr5:96192413-96192414
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr5:96142198..96144111-chr5:96191264..96193895,2	MCF-7	breast:
2	chr5:96185451..96187318-chr5:96190686..96192448,2	K562	blood:
3	chr5:96187112..96188825-chr5:96189187..96193185,3	MCF-7	breast:
4	chr5:96184835..96188350-chr5:96188739..96192448,3	K562	blood:

Variant related genes	Relation type
ENSG00000164307	Chromatin interaction

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs149598	0.93[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs152469	0.93[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs249959	0.93[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs26494	0.93[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs26520	0.93[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs27530	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs27690	0.84[EUR][1000 genomes]
rs27895	0.81[EUR][1000 genomes]
rs28046	0.84[EUR][1000 genomes]
rs34733	0.93[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs34734	0.93[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs34736	0.93[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs40089	0.93[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs57298362	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs57663955	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs58587603	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59832415	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs60376893	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60792454	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs61227121	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs647031	0.93[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7708451	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv432755	chr5:95987984-96657483	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
2	nsv598962	chr5:96057891-96893164	Weak transcription Strong transcription Enhancers Bivalent/Poised TSS Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
3	nsv516293	chr5:96070205-96216387	Strong transcription Flanking Active TSS Weak transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
4	nsv948703	chr5:96078309-96368839	Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
5	nsv1027472	chr5:96081592-96337550	Strong transcription Genic enhancers Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
6	nsv1028741	chr5:96082401-96372165	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
7	nsv949058	chr5:96082433-96390619	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
8	nsv598963	chr5:96084776-96363407	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
9	nsv432756	chr5:96113844-96234644	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
10	nsv531967	chr5:96127842-96302702	Flanking Active TSS Strong transcription Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:96188800-96193000	Enhancers	Fetal Intestine Small	intestine
2	chr5:96188800-96194400	Enhancers	Adipose Nuclei	Adipose
3	chr5:96189800-96196400	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr5:96191200-96192600	Enhancers	Fetal Lung	lung
5	chr5:96191200-96192600	Enhancers	Fetal Muscle Leg	muscle
6	chr5:96191400-96192800	Enhancers	Fetal Stomach	stomach
7	chr5:96191600-96192600	Enhancers	Small Intestine	intestine
8	chr5:96191600-96192800	Enhancers	Rectal Mucosa Donor 31	rectum
9	chr5:96191600-96193000	Enhancers	Fetal Intestine Large	intestine
10	chr5:96191600-96193000	Enhancers	Skeletal Muscle Female	skeletal muscle
11	chr5:96191800-96192600	Enhancers	Rectal Mucosa Donor 29	rectum
12	chr5:96191800-96193000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr5:96191800-96194400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr5:96192200-96192600	Enhancers	Stomach Smooth Muscle	stomach
15	chr5:96192200-96192800	Enhancers	Psoas Muscle	Psoas
16	chr5:96192200-96193000	Enhancers	Fetal Thymus	thymus
17	chr5:96192400-96192600	Enhancers	Thymus	Thymus
18	chr5:96192400-96193000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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