Variant report

Variant	rs429041
Chromosome Location	chr14:36541136-36541137
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	chr14:36538483..36541249-chr14:36788541..36791272,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000151332	Chromatin interaction

Extended variants
information (count: 39 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11156905	0.80[EUR][1000 genomes]
rs1333312	0.82[EUR][1000 genomes]
rs1742867	0.96[CEU][hapmap];0.99[EUR][1000 genomes]
rs1742868	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1742869	1.00[CEU][hapmap];0.82[EUR][1000 genomes]
rs1742876	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2780313	0.88[CEU][hapmap];0.83[JPT][hapmap];0.85[EUR][1000 genomes]
rs2780314	0.85[CEU][hapmap]
rs367883	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs368181	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs368187	0.81[EUR][1000 genomes]
rs368772	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs371191	0.89[EUR][1000 genomes]
rs375095	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs394246	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs395212	0.96[CEU][hapmap];0.99[EUR][1000 genomes]
rs395660	0.90[EUR][1000 genomes]
rs396043	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs398745	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs408783	0.99[EUR][1000 genomes]
rs410546	0.99[EUR][1000 genomes]
rs448145	0.96[CEU][hapmap];0.99[EUR][1000 genomes]
rs4981320	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6571735	0.96[CEU][hapmap];0.91[CHB][hapmap];0.95[JPT][hapmap];0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7145211	0.96[CEU][hapmap]
rs7145546	0.96[CEU][hapmap]
rs7147401	1.00[CEU][hapmap]
rs8003253	0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs8007617	0.84[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs8008989	0.84[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs8020453	0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs847514	0.96[EUR][1000 genomes]
rs847516	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs860200	0.82[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1051045	chr14:36116503-36764947	Weak transcription Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
2	nsv542038	chr14:36116503-36764947	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
3	nsv1051147	chr14:36413342-36562863	Enhancers Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv1040256	chr14:36501452-37172046	Strong transcription Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
5	nsv542040	chr14:36501452-37172046	Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	45 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	chr14:36539600-36542000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr14:36539600-36542000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr14:36539800-36542200	Weak transcription	Brain Cingulate Gyrus	brain
4	chr14:36539800-36542200	Weak transcription	Brain Substantia Nigra	brain

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