Variant report

Variant	rs13059815
Chromosome Location	chr3:81616398-81616399
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	chr3:81605753..81607787-chr3:81613884..81616486,2	MCF-7	breast:

Extended variants
information (count: 60 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs1031265	0.85[JPT][hapmap]
rs11917558	0.83[CHB][hapmap];0.82[YRI][hapmap]
rs12631775	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12638726	0.95[CEU][hapmap];0.95[JPT][hapmap];0.81[YRI][hapmap];0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs13063700	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13082939	0.85[JPT][hapmap]
rs13086984	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[YRI][hapmap];0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13087181	0.91[JPT][hapmap]
rs13088641	0.90[JPT][hapmap]
rs13092113	0.86[JPT][hapmap]
rs13097903	0.85[JPT][hapmap]
rs1381302	0.91[JPT][hapmap]
rs1381303	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1461606	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs17019039	0.90[JPT][hapmap]
rs17019042	0.91[JPT][hapmap]
rs2307058	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2639611	0.95[CEU][hapmap];0.95[JPT][hapmap];0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs34567512	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs35058426	0.84[ASN][1000 genomes]
rs59299387	0.81[ASN][1000 genomes]
rs6764261	0.83[CHB][hapmap]
rs6768592	0.86[JPT][hapmap]
rs6768895	0.95[CEU][hapmap];0.95[JPT][hapmap];0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6769105	0.95[CEU][hapmap];0.95[JPT][hapmap];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6769140	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6769230	0.94[CEU][hapmap];0.95[JPT][hapmap];0.82[YRI][hapmap];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6773695	0.95[CEU][hapmap];0.95[JPT][hapmap]
rs6785586	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6798069	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs6798900	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6800241	0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6805105	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7610703	0.83[CHB][hapmap];0.82[YRI][hapmap]
rs7613144	1.00[CEU][hapmap];0.87[CHB][hapmap];0.90[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7615728	0.83[ASN][1000 genomes]
rs7616817	0.95[CEU][hapmap];0.95[JPT][hapmap];0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7618973	0.83[CHB][hapmap]
rs7622741	0.94[CEU][hapmap];0.95[JPT][hapmap];0.89[YRI][hapmap];0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7631349	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7637268	0.95[CEU][hapmap];0.80[CHB][hapmap];0.95[JPT][hapmap];0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7649028	0.94[CEU][hapmap];0.95[JPT][hapmap];0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs820275	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9811029	1.00[JPT][hapmap];0.80[YRI][hapmap];0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9811835	0.95[CEU][hapmap];0.95[JPT][hapmap];0.81[YRI][hapmap];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9815059	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9818063	0.83[ASN][1000 genomes]
rs9820815	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9845467	0.83[CHB][hapmap]
rs9853643	0.95[CEU][hapmap];0.80[CHB][hapmap];0.95[JPT][hapmap];0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9867226	0.84[ASN][1000 genomes]
rs9871529	0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv934018	chr3:81413060-81655338	Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv933756	chr3:81413060-81754738	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv1003217	chr3:81435044-81752521	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv1012133	chr3:81499082-81817471	ZNF genes & repeats Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
5	nsv933259	chr3:81523854-81730617	Enhancers Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
6	nsv949545	chr3:81523898-81893929	Strong transcription Weak transcription Active TSS Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
7	nsv999587	chr3:81534364-81707800	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
8	nsv536603	chr3:81534364-81707800	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:81581600-81628200	Weak transcription	Stomach Smooth Muscle	stomach
2	chr3:81583600-81625600	Weak transcription	HUVEC	blood vessel
3	chr3:81584200-81636600	Weak transcription	Placenta	Placenta
4	chr3:81598200-81625600	Weak transcription	Duodenum Smooth Muscle	Duodenum
5	chr3:81603600-81726400	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr3:81604200-81641200	Weak transcription	HSMMtube	muscle
7	chr3:81608600-81644000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
8	chr3:81609200-81636600	Weak transcription	Pancreas	Pancrea
9	chr3:81609400-81635200	Weak transcription	Duodenum Mucosa	Duodenum
10	chr3:81610800-81624000	Strong transcription	Dnd41	blood
11	chr3:81611600-81628600	Weak transcription	Spleen	Spleen
12	chr3:81611600-81629000	Weak transcription	NHLF	lung
13	chr3:81612000-81630400	Weak transcription	Rectal Mucosa Donor 29	rectum
14	chr3:81612800-81626800	Weak transcription	Osteobl	bone
15	chr3:81612800-81631000	Weak transcription	Fetal Kidney	kidney
16	chr3:81613000-81622800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr3:81613600-81618600	Weak transcription	Muscle Satellite Cultured Cells	--
18	chr3:81613600-81625800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr3:81613600-81699200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr3:81614000-81616600	Weak transcription	NHDF-Ad	bronchial
21	chr3:81614000-81623000	Weak transcription	Primary neutrophils fromperipheralblood	blood
22	chr3:81614000-81625600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr3:81614000-81629600	Weak transcription	Psoas Muscle	Psoas
24	chr3:81614000-81638200	Weak transcription	Lung	lung
25	chr3:81614000-81693600	Weak transcription	Aorta	Aorta
26	chr3:81614200-81619600	Weak transcription	Adipose Nuclei	Adipose
27	chr3:81614200-81625800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
28	chr3:81614200-81627000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr3:81614200-81628800	Weak transcription	Skeletal Muscle Male	skeletal muscle
30	chr3:81614200-81640400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
31	chr3:81614400-81622600	Weak transcription	Liver	Liver
32	chr3:81614400-81625600	Weak transcription	Skeletal Muscle Female	skeletal muscle
33	chr3:81614400-81625800	Weak transcription	Ovary	ovary
34	chr3:81614400-81627000	Weak transcription	HepG2	liver
35	chr3:81614400-81629600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr3:81614400-81643600	Weak transcription	Primary T cells from cord blood	blood
37	chr3:81614400-81688800	Weak transcription	Right Ventricle	heart
38	chr3:81614600-81618800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr3:81614600-81625600	Weak transcription	Primary B cells from cord blood	blood
40	chr3:81614600-81633400	Weak transcription	Primary hematopoietic stem cells	blood
41	chr3:81614600-81634200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr3:81614800-81618000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
43	chr3:81614800-81620800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr3:81614800-81625600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr3:81615600-81616400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr3:81615600-81616400	Strong transcription	Left Ventricle	heart
47	chr3:81616000-81616600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr3:81616000-81619400	Weak transcription	Primary B cells from peripheral blood	blood
49	chr3:81616000-81623600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr3:81616200-81616800	Strong transcription	HSMM	muscle

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