Variant report

Variant	rs4303249
Chromosome Location	chr11:87297791-87297792
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 83 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:76)

rs_ID	r²[population]
rs1010309	0.96[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs10501641	0.92[ASN][1000 genomes]
rs10898739	0.99[AFR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10898742	0.99[AFR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11235191	0.92[ASN][1000 genomes]
rs11235193	0.92[ASN][1000 genomes]
rs11235200	0.92[ASN][1000 genomes]
rs11235201	0.92[ASN][1000 genomes]
rs11235204	0.92[ASN][1000 genomes]
rs11235221	0.99[AFR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11235224	0.96[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs11235225	1.00[ASN][1000 genomes]
rs11494293	0.99[AFR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11494294	0.99[AFR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11601376	0.92[ASN][1000 genomes]
rs11604094	0.88[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs12361220	0.99[AFR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17760207	0.92[ASN][1000 genomes]
rs1880116	0.98[AFR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2212948	0.99[AFR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2212949	0.97[AFR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2375040	0.92[ASN][1000 genomes]
rs2375041	0.92[ASN][1000 genomes]
rs2375042	0.92[ASN][1000 genomes]
rs28370470	0.96[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs28702774	1.00[ASN][1000 genomes]
rs4245435	0.89[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs4278537	0.96[AFR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4284412	0.99[AFR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4338554	0.92[ASN][1000 genomes]
rs4414247	0.92[ASN][1000 genomes]
rs4438065	0.92[ASN][1000 genomes]
rs4536254	0.89[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs4548644	0.93[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs4622295	0.99[AFR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4943986	0.86[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs4943987	0.89[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs4944711	0.85[ASN][1000 genomes]
rs4944712	0.92[ASN][1000 genomes]
rs4944715	0.92[ASN][1000 genomes]
rs4944721	0.89[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs4944723	0.98[AFR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4944724	0.98[AFR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4944725	0.98[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs5010075	0.92[ASN][1000 genomes]
rs6592386	0.99[AFR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6592387	0.99[AFR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6592393	0.96[AFR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6592394	0.96[AFR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67701569	0.92[ASN][1000 genomes]
rs7105478	0.96[AFR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7121065	0.92[ASN][1000 genomes]
rs7124539	0.99[AFR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7124569	0.92[ASN][1000 genomes]
rs7126228	0.96[AFR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7126694	0.91[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs7127253	0.99[AFR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72965616	0.85[ASN][1000 genomes]
rs72965688	0.87[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs72967546	0.96[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs72967550	0.92[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs7924614	0.96[AFR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7924814	0.96[AFR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7927078	0.83[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs7929162	0.99[AFR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7930759	0.94[AFR][1000 genomes]
rs7930765	0.88[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs7930820	0.99[AFR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7931538	0.96[AFR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7931854	0.96[AFR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7934337	0.89[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs7936294	0.83[AFR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7940053	0.96[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs7944286	0.99[AFR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7947181	0.92[ASN][1000 genomes]
rs7949528	0.98[AFR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1043562	chr11:86755535-87547185	Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
2	nsv541120	chr11:86755535-87547185	Bivalent Enhancer Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
3	nsv555714	chr11:87058981-87399218	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv1039172	chr11:87068731-87385458	Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv832224	chr11:87162121-87355923	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
6	nsv898075	chr11:87278074-87375119	Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region CpG island	2 gene(s)	inside rSNPs	diseases
7	esv2760195	chr11:87295119-87329156	Weak transcription Enhancers	TF binding region	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:87296400-87313600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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