Variant report

Variant	rs572545
Chromosome Location	chr13:53433329-53433330
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr13:53423269..53426675-chr13:53427472..53433524,8	MCF-7	breast:
2	chr13:53432415..53433397-chr7:61969357..61970027,2	MCF-7	breast:
3	chr13:53425388..53426892-chr13:53431589..53434414,2	MCF-7	breast:

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs12100313	0.95[ASN][1000 genomes]
rs1274580	0.95[ASN][1000 genomes]
rs1274581	0.96[ASN][1000 genomes]
rs1274582	0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1323117	0.82[ASN][1000 genomes]
rs1359046	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1885848	0.96[ASN][1000 genomes]
rs1923853	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2764035	0.96[ASN][1000 genomes]
rs2897999	0.96[ASN][1000 genomes]
rs471680	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs489654	0.80[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs496890	0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs508523	0.96[ASN][1000 genomes]
rs525135	0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs537874	0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs540528	0.96[ASN][1000 genomes]
rs582583	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs604105	0.80[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs615225	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs629671	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs636937	0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs646902	0.96[ASN][1000 genomes]
rs648146	0.95[ASN][1000 genomes]
rs648232	0.80[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs649523	0.96[ASN][1000 genomes]
rs664608	0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs676284	0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9316593	0.80[ASN][1000 genomes]
rs9591474	0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9596705	0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9596709	0.98[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9596710	0.98[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9788390	0.95[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	nsv530719	chr13:53173014-53675953	Weak transcription Flanking Bivalent TSS/Enh Enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
2	esv3440613	chr13:53307609-53671072	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
3	esv1810064	chr13:53412849-53441018	Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	7 gene(s)	inside rSNPs	diseases
4	esv1822518	chr13:53412849-53441018	Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region miRNA target site	7 gene(s)	inside rSNPs	diseases
5	esv1829072	chr13:53412849-53441018	Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region miRNA target site	7 gene(s)	inside rSNPs	diseases
6	nsv455889	chr13:53419139-53466127	Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Weak transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
7	nsv561661	chr13:53419139-53466127	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
8	nsv900090	chr13:53429453-53495715	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS	Chromatin interactive region	1 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	chr13:53426000-53437000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr13:53426800-53433800	Weak transcription	Dnd41	blood
3	chr13:53430400-53434000	Weak transcription	GM12878-XiMat	blood
4	chr13:53430800-53441400	Weak transcription	iPS-18 Cell Line	embryonic stem cell

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