Variant report

Variant	rs59436713
Chromosome Location	chr10:51531440-51531441
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:10)
CpG islands
(count:0)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:10 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	GATA3	chr10:51531043-51531604	T-47D	breast:	n/a	n/a
2	FOXA1	chr10:51531329-51531660	T-47D	breast:	n/a	n/a
3	FOXA1	chr10:51531060-51531642	T-47D	breast:	n/a	n/a
4	NR2F2	chr10:51531020-51531629	MCF-7	breast:	n/a	n/a
5	GATA3	chr10:51530997-51531674	MCF-7	breast:	n/a	n/a
6	FOXA2	chr10:51531089-51531520	HepG2	liver:	n/a	n/a
7	GATA3	chr10:51530993-51531674	MCF-7	breast:	n/a	n/a
8	FOXA1	chr10:51531002-51531564	HepG2	liver:	n/a	n/a
9	GATA3	chr10:51530991-51531591	T-47D	breast:	n/a	n/a
10	EP300	chr10:51531105-51531512	T-47D	breast:	n/a	n/a

No data

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:51531433..51533993-chr10:51534075..51536056,4	MCF-7	breast:
2	chr10:51529724..51536582-chr10:51546578..51552342,12	MCF-7	breast:
3	chr10:51529774..51532787-chr10:51533205..51535584,3	K562	blood:

No data

No data

No data

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs11003820	1.00[AMR][1000 genomes]
rs11004361	1.00[AMR][1000 genomes]
rs11004455	1.00[AMR][1000 genomes]
rs11005274	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11005729	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12246321	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12247763	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12249198	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12250658	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16914406	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16914420	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56301424	1.00[AMR][1000 genomes]
rs60528425	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74131171	1.00[AMR][1000 genomes]
rs74131182	0.88[AFR][1000 genomes];1.00[AMR][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	esv2758219	chr10:50971974-51925166	Enhancers Active TSS Transcr. at gene 5' and 3' Strong transcription Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
2	esv2759749	chr10:50971974-51925166	Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
3	nsv428232	chr10:50971974-51925166	Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
4	esv1830900	chr10:51187411-51903662	Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
5	nsv895383	chr10:51260747-51724915	Strong transcription Enhancers Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
6	nsv1048474	chr10:51330433-51545872	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
7	nsv508583	chr10:51385007-51595892	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
8	esv1815597	chr10:51525699-51804254	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent Enhancer 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	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:51525000-51540000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr10:51525800-51532400	Weak transcription	Monocytes-CD14+_RO01746	blood
3	chr10:51527200-51539800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr10:51529600-51531600	Enhancers	HepG2	liver
5	chr10:51531400-51531800	Enhancers	Stomach Mucosa	stomach

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dbSNP/dbVar ID: rs12345 /nsv7879
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