Variant report

Variant	rs13253537
Chromosome Location	chr8:85408696-85408697
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:85406795..85409565-chr8:85418186..85421161,2	MCF-7	breast:

Extended variants
information (count: 87 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:84)

rs_ID	r²[population]
rs1021852	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1021853	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10453097	0.97[ASN][1000 genomes]
rs10504803	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs10504805	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[ASN][1000 genomes]
rs12114244	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs1319379	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs13248532	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs13252091	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs13255463	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs13256410	0.98[ASN][1000 genomes]
rs13257448	0.98[ASN][1000 genomes]
rs13259587	0.97[ASN][1000 genomes]
rs13261209	0.97[ASN][1000 genomes]
rs13265396	0.89[ASN][1000 genomes]
rs13271249	0.97[ASN][1000 genomes]
rs13275430	0.95[ASN][1000 genomes]
rs1351223	0.92[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.90[YRI][hapmap];0.82[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs1393990	0.89[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap]
rs1479092	0.90[CEU][hapmap];0.87[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs1479093	0.89[CEU][hapmap];0.87[CHB][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs1479094	0.90[CEU][hapmap];0.95[JPT][hapmap]
rs1479096	0.86[CEU][hapmap];0.95[JPT][hapmap]
rs1479098	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap];0.83[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs1503602	0.95[ASN][1000 genomes]
rs1564314	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1564315	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1564316	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1566791	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs1566792	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1824887	0.86[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.94[AFR][1000 genomes];0.84[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs1847344	0.92[CEU][hapmap];0.80[CHB][hapmap];1.00[JPT][hapmap]
rs1947960	0.92[CEU][hapmap];0.83[CHB][hapmap];1.00[JPT][hapmap]
rs1994149	0.82[CHB][hapmap];0.83[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.84[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs2046313	0.83[ASN][1000 genomes]
rs2127218	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs2169922	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs28751114	0.97[ASN][1000 genomes]
rs317947	0.86[JPT][hapmap]
rs4739691	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs4740014	1.00[ASN][1000 genomes]
rs4740015	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.88[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4740016	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs4740017	1.00[ASN][1000 genomes]
rs4740018	0.92[CEU][hapmap];0.95[JPT][hapmap]
rs4740019	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4740020	0.97[ASN][1000 genomes]
rs4740021	0.82[ASN][1000 genomes]
rs4740022	0.96[ASN][1000 genomes]
rs4740023	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs4740024	0.92[ASN][1000 genomes]
rs60533047	0.92[ASN][1000 genomes]
rs6473552	0.98[AFR][1000 genomes];0.88[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6473553	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs6473554	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6473555	0.90[CEU][hapmap]
rs7011638	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs7013087	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs711002	0.87[CHB][hapmap];0.86[JPT][hapmap]
rs711006	0.87[CHB][hapmap];0.86[JPT][hapmap]
rs711007	1.00[JPT][hapmap];0.82[YRI][hapmap];0.86[ASN][1000 genomes]
rs711011	0.95[CHB][hapmap];1.00[JPT][hapmap];0.87[YRI][hapmap];0.95[ASN][1000 genomes]
rs711025	0.86[AFR][1000 genomes];0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs711027	1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap];0.90[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs711032	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs711033	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs711041	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs711048	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs711052	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs711054	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs711059	0.85[CHB][hapmap];1.00[JPT][hapmap]
rs711060	1.00[JPT][hapmap]
rs7820792	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs7822198	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7822220	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7829180	0.90[ASN][1000 genomes]
rs783507	0.86[CHB][hapmap];0.85[JPT][hapmap]
rs783508	0.87[CHB][hapmap];0.86[JPT][hapmap]
rs783509	0.86[CHB][hapmap];0.85[JPT][hapmap]
rs783788	0.87[CHB][hapmap];0.86[JPT][hapmap]
rs783789	0.87[CHB][hapmap];0.86[JPT][hapmap]
rs783791	0.85[JPT][hapmap]
rs7845599	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[YRI][hapmap];0.93[AFR][1000 genomes];0.88[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9298424	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv831375	chr8:85272352-85463621	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
2	esv3481417	chr8:85279453-86145229	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
3	esv3481418	chr8:85279453-86145229	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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