Variant report

Variant	rs10785665
Chromosome Location	chr12:47583708-47583709
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr12:47498470..47501746-chr12:47583705..47586367,3	MCF-7	breast:
2	chr12:47579225..47581845-chr12:47583061..47584713,2	MCF-7	breast:
3	chr12:47582918..47584527-chr12:47660728..47663353,2	MCF-7	breast:
4	chr12:47583159..47586380-chr12:47586604..47590176,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000263838	Chromatin interaction

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10736032	0.86[EUR][1000 genomes]
rs10785664	1.00[CEU][hapmap];0.90[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10785667	0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10785668	0.96[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10881066	0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10881067	0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10881068	0.81[ASN][1000 genomes]
rs10881069	1.00[CEU][hapmap];0.90[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10881070	1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10881071	0.85[ASN][1000 genomes]
rs10881072	0.86[CHB][hapmap];0.95[JPT][hapmap];0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11183738	1.00[YRI][hapmap]
rs11183750	1.00[YRI][hapmap]
rs11183752	1.00[YRI][hapmap]
rs11183777	1.00[YRI][hapmap]
rs11183783	1.00[YRI][hapmap]
rs12368600	1.00[YRI][hapmap]
rs1404817	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1404818	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1554693	1.00[YRI][hapmap]
rs17821774	1.00[YRI][hapmap]
rs1917657	1.00[YRI][hapmap]
rs4768142	1.00[YRI][hapmap]
rs4768143	1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4768778	1.00[CEU][hapmap];0.90[CHB][hapmap];0.85[JPT][hapmap];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4768779	1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4768780	0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4768781	1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4768782	1.00[YRI][hapmap]
rs4768783	0.83[CEU][hapmap];0.86[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv469368	chr12:47374908-47675680	Enhancers Genic enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
2	nsv558784	chr12:47374908-47675680	Genic enhancers Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
3	nsv832399	chr12:47502910-47689601	Genic enhancers Enhancers Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
4	esv2751100	chr12:47541390-47746157	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	45 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:84 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:47578200-47587800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr12:47578400-47583800	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr12:47579200-47584000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr12:47579400-47583800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr12:47579400-47584200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
6	chr12:47579400-47584400	Weak transcription	Esophagus	oesophagus
7	chr12:47580200-47584400	Enhancers	Primary T killer memory cells from peripheral blood	blood
8	chr12:47580400-47584000	Enhancers	Primary T helper cells PMA-I stimulated	--
9	chr12:47580400-47584400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
10	chr12:47580800-47585600	Enhancers	Primary T helper cells fromperipheralblood	blood
11	chr12:47581000-47585800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
12	chr12:47581800-47584600	Enhancers	Liver	Liver
13	chr12:47581800-47594000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
14	chr12:47582000-47585400	Enhancers	Monocytes-CD14+_RO01746	blood
15	chr12:47582200-47583800	Enhancers	NHDF-Ad	bronchial
16	chr12:47582200-47584200	Genic enhancers	Primary B cells from peripheral blood	blood
17	chr12:47582200-47584600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr12:47582200-47584600	Genic enhancers	Primary T cells from cord blood	blood
19	chr12:47582200-47584800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr12:47582200-47584800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr12:47582200-47584800	Enhancers	K562	blood
22	chr12:47582200-47585000	Enhancers	NH-A	brain
23	chr12:47582200-47585000	Enhancers	Osteobl	bone
24	chr12:47582200-47585400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
25	chr12:47582200-47585600	Enhancers	Primary monocytes fromperipheralblood	blood
26	chr12:47582400-47583800	Enhancers	Fetal Lung	lung
27	chr12:47582400-47583800	Enhancers	Lung	lung
28	chr12:47582400-47583800	Enhancers	Rectal Mucosa Donor 31	rectum
29	chr12:47582400-47583800	Enhancers	Small Intestine	intestine
30	chr12:47582400-47583800	Enhancers	Hela-S3	cervix
31	chr12:47582400-47584000	Enhancers	GM12878-XiMat	blood
32	chr12:47582400-47584200	Enhancers	Right Atrium	heart
33	chr12:47582400-47584400	Enhancers	HUVEC	blood vessel
34	chr12:47582400-47584600	Genic enhancers	Primary T cells fromperipheralblood	blood
35	chr12:47582400-47584600	Enhancers	Adipose Nuclei	Adipose
36	chr12:47582400-47584600	Enhancers	Duodenum Mucosa	Duodenum
37	chr12:47582400-47584600	Enhancers	Gastric	stomach
38	chr12:47582400-47584600	Enhancers	Spleen	Spleen
39	chr12:47582400-47584800	Enhancers	Left Ventricle	heart
40	chr12:47582400-47584800	Enhancers	HSMM	muscle
41	chr12:47582400-47585200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr12:47582400-47585400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr12:47582400-47585400	Enhancers	Primary hematopoietic stem cells short term culture	blood
44	chr12:47582400-47585400	Enhancers	NHEK	skin
45	chr12:47582600-47583800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr12:47582600-47584400	Enhancers	Duodenum Smooth Muscle	Duodenum
47	chr12:47582600-47584600	Enhancers	Ovary	ovary
48	chr12:47582600-47584800	Flanking Active TSS	A549	lung
49	chr12:47582600-47585400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
50	chr12:47582800-47584000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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