Variant report

Variant	rs11707957
Chromosome Location	chr3:159148909-159148910
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:159147245..159149720-chr3:159151129..159153409,4	MCF-7	breast:

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs11706209	0.81[AMR][1000 genomes]
rs11715734	0.96[CEU][hapmap]
rs1375403	1.00[CEU][hapmap];0.90[EUR][1000 genomes]
rs1375404	0.90[EUR][1000 genomes]
rs1375405	1.00[CEU][hapmap];0.89[EUR][1000 genomes]
rs1448998	0.96[CEU][hapmap]
rs1449012	0.93[CEU][hapmap]
rs1449024	0.96[CEU][hapmap]
rs1562671	0.96[CEU][hapmap]
rs1562672	0.89[CEU][hapmap]
rs17795566	0.86[CEU][hapmap]
rs1975601	0.89[CEU][hapmap]
rs2595243	0.89[CEU][hapmap]
rs2595244	0.89[CEU][hapmap]
rs2595245	0.86[CEU][hapmap]
rs2595246	0.92[CEU][hapmap]
rs2595247	0.86[CEU][hapmap]
rs2595248	0.92[CEU][hapmap]
rs2621290	0.89[CEU][hapmap]
rs2621297	0.89[CEU][hapmap]
rs2621299	0.86[CEU][hapmap]
rs2621300	0.86[CEU][hapmap]
rs2621310	0.89[CEU][hapmap]
rs2621312	0.85[CEU][hapmap]
rs2621313	0.86[CEU][hapmap]
rs2621314	0.89[CEU][hapmap]
rs3851358	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4680500	0.92[CEU][hapmap]
rs4680504	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4680505	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6441255	1.00[CEU][hapmap];0.90[EUR][1000 genomes]
rs6782867	0.96[CEU][hapmap]
rs6790560	0.96[CEU][hapmap]
rs6807076	0.96[CEU][hapmap];0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs73166247	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs733904	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7428369	0.96[CEU][hapmap];0.87[EUR][1000 genomes]
rs7646959	0.96[CEU][hapmap];0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7649056	0.96[CEU][hapmap]
rs9875283	1.00[CHB][hapmap];1.00[JPT][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	nsv470971	chr3:158590928-159158217	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
2	nsv998949	chr3:158774806-159394550	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	4 gene(s)	inside rSNPs	diseases
3	nsv1004990	chr3:159090974-159174954	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive 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	chr3:159147800-159149000	Weak transcription	Fetal Brain Male	brain

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