Variant report

Variant	rs13278361
Chromosome Location	chr8:104269649-104269650
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	chr8:104268461..104270689-chr8:104277441..104279218,2	MCF-7	breast:

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs1138873	0.90[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs12541167	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12543038	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs13275377	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13278540	0.90[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs1353212	0.97[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1353213	0.97[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1403293	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1494278	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1522707	0.84[AMR][1000 genomes]
rs1568641	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs16870243	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs16870245	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs16870249	0.93[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs17205332	1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs17799604	0.85[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs1982892	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1982893	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2220825	0.97[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2270525	0.83[AMR][1000 genomes]
rs3104029	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs3104031	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs3107646	0.89[AMR][1000 genomes]
rs3107648	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs3107649	0.80[AMR][1000 genomes]
rs3116457	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs3116462	0.88[AMR][1000 genomes]
rs3116464	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs3116466	0.87[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs3116468	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs3133820	0.87[AMR][1000 genomes]
rs3133821	0.87[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs3133824	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3133825	0.80[AMR][1000 genomes]
rs34185273	0.97[AMR][1000 genomes];0.88[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs34201011	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs34273148	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34337822	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4734693	0.82[ASN][1000 genomes]
rs4734695	0.92[ASN][1000 genomes]
rs9656787	0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv831413	chr8:104085141-104269789	Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	28 gene(s)	inside rSNPs	diseases
2	nsv429931	chr8:104097396-104878014	Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	82 gene(s)	inside rSNPs	diseases
3	esv1848810	chr8:104128496-104369288	Strong transcription Enhancers Weak transcription Genic enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
4	esv1844303	chr8:104128696-104369090	Genic enhancers Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
5	nsv1015965	chr8:104192086-104361108	Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
6	nsv1017326	chr8:104236193-104313235	Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Enhancers Weak transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:26 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:104252200-104279000	Weak transcription	Aorta	Aorta
2	chr8:104264200-104271600	Weak transcription	Primary hematopoietic stem cells	blood
3	chr8:104266400-104269800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr8:104266400-104270200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr8:104266600-104270000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr8:104266600-104270600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr8:104266800-104270200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr8:104267200-104269800	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr8:104267200-104269800	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chr8:104267400-104269800	Enhancers	Brain Substantia Nigra	brain
11	chr8:104267600-104270000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr8:104267800-104270000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr8:104268000-104269800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr8:104268200-104283400	Weak transcription	H9 Cell Line	embryonic stem cell
15	chr8:104268600-104270000	Enhancers	Primary neutrophils fromperipheralblood	blood
16	chr8:104268800-104281200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr8:104269000-104270000	Weak transcription	HUES64 Cell Line	embryonic stem cell
18	chr8:104269000-104271800	Weak transcription	Hela-S3	cervix
19	chr8:104269000-104272400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr8:104269000-104283400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr8:104269200-104269800	Active TSS	Brain Cingulate Gyrus	brain
22	chr8:104269600-104269800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr8:104269600-104269800	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr8:104269600-104269800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr8:104269600-104269800	Enhancers	Lung	lung
26	chr8:104269600-104270200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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