Variant report

Variant	rs72711284
Chromosome Location	chr15:45816024-45816025
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr15:45813492..45816353-chr15:45876550..45880712,4	MCF-7	breast:
2	chr15:45801393..45804941-chr15:45813631..45816253,3	MCF-7	breast:
3	chr15:45813395..45816326-chr15:45879088..45881474,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000104164	Chromatin interaction
ENSG00000179362	Chromatin interaction
ENSG00000260170	Chromatin interaction

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs1153830	0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1153831	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1153832	0.85[ASN][1000 genomes]
rs16944629	0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1768458	0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2088164	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2433600	1.00[AMR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2433617	0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2433619	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs35828336	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4448883	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs55997350	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs56179992	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs56405528	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs59574269	0.91[EUR][1000 genomes]
rs60350201	0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs60992352	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs61193305	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6493154	0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6493157	0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6493158	0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6493160	0.94[EUR][1000 genomes]
rs7165838	0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7169748	0.94[EUR][1000 genomes]
rs7171406	0.94[EUR][1000 genomes]
rs7173983	0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs72711264	0.86[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs72711278	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72711279	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72711280	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72711283	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72711290	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72711294	0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs72711301	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs72713103	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs72713104	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs72713105	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs8023437	0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs8025407	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs8029509	0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs8040466	0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs8042811	0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]

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	nsv932147	chr15:45319178-45872076	Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
2	nsv1045556	chr15:45777396-45884854	Strong transcription Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
3	nsv904188	chr15:45801035-45941689	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Strong transcription 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	57 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	chr15:45815600-45818400	Weak transcription	Primary B cells from peripheral blood	blood
2	chr15:45815600-45825000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr15:45815800-45818400	Weak transcription	Rectal Mucosa Donor 31	rectum
4	chr15:45815800-45819000	Weak transcription	Duodenum Mucosa	Duodenum

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