Variant report

Variant	rs59363486
Chromosome Location	chr8:6425766-6425767
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	MAFK	chr8:6425759-6426131	HepG2	liver:	n/a	chr8:6425922-6425942 chr8:6426023-6426034 chr8:6425927-6425943 chr8:6426024-6426035 chr8:6425924-6425940 chr8:6426024-6426035 chr8:6425927-6425942 chr8:6425925-6425939
2	MAFF	chr8:6425755-6426110	HepG2	liver:	n/a	chr8:6425926-6425944 chr8:6425925-6425939
3	MAFK	chr8:6425754-6426104	IMR90	lung:	n/a	chr8:6425922-6425942 chr8:6426023-6426034 chr8:6425927-6425943 chr8:6426024-6426035 chr8:6425924-6425940 chr8:6426024-6426035 chr8:6425927-6425942 chr8:6425925-6425939
4	POLR2A	chr8:6425710-6425766	MCF-7	breast:	n/a	n/a
5	MAFK	chr8:6425751-6426118	HepG2	liver:	n/a	chr8:6425922-6425942 chr8:6426023-6426034 chr8:6425927-6425943 chr8:6426024-6426035 chr8:6425924-6425940 chr8:6426024-6426035 chr8:6425927-6425942 chr8:6425925-6425939

Variant related genes	Relation type
ANGPT2	TF binding region

Extended variants
information (count: 46 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs10103026	0.85[EUR][1000 genomes]
rs10481362	0.92[EUR][1000 genomes]
rs17077547	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2012093	0.92[EUR][1000 genomes]
rs28539969	0.85[EUR][1000 genomes]
rs2922808	0.85[EUR][1000 genomes]
rs2922864	0.85[EUR][1000 genomes]
rs2922865	0.92[EUR][1000 genomes]
rs2922884	0.85[EUR][1000 genomes]
rs2922888	0.92[EUR][1000 genomes]
rs2922890	0.85[EUR][1000 genomes]
rs2922893	0.85[EUR][1000 genomes]
rs2922894	0.85[EUR][1000 genomes]
rs2959763	0.85[EUR][1000 genomes]
rs2959764	0.85[EUR][1000 genomes]
rs2959765	0.85[EUR][1000 genomes]
rs2959767	0.85[EUR][1000 genomes]
rs2959771	1.00[EUR][1000 genomes]
rs3020227	0.85[EUR][1000 genomes]
rs3020230	0.85[EUR][1000 genomes]
rs3020231	0.85[EUR][1000 genomes]
rs3020232	0.85[EUR][1000 genomes]
rs3020233	0.85[EUR][1000 genomes]
rs3020234	0.85[EUR][1000 genomes]
rs3020235	0.85[EUR][1000 genomes]
rs3020236	0.85[EUR][1000 genomes]
rs6981002	0.92[EUR][1000 genomes]
rs6991221	0.85[EUR][1000 genomes]
rs7004238	0.85[EUR][1000 genomes]
rs73509235	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73661410	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9314604	0.85[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv890034	chr8:5926632-6427868	Enhancers Strong transcription Active TSS Genic enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv1021175	chr8:5965453-6880364	Enhancers Flanking Active TSS Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
3	nsv1027682	chr8:6018123-6920312	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
4	esv3506199	chr8:6116693-6536592	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	11 gene(s)	inside rSNPs	diseases
5	esv3506200	chr8:6116693-6536592	Active TSS Strong transcription Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	11 gene(s)	inside rSNPs	diseases
6	nsv933282	chr8:6261036-6440592	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
7	nsv1015981	chr8:6286575-6578450	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	17 gene(s)	inside rSNPs	diseases
8	nsv1027313	chr8:6286575-6920312	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
9	nsv890057	chr8:6317165-6427868	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
10	nsv1021684	chr8:6350091-6809455	Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
11	esv2422383	chr8:6362389-6781593	Enhancers Bivalent Enhancer Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
12	nsv610004	chr8:6402366-6772913	Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
13	nsv1029241	chr8:6411300-6761720	Weak transcription Strong transcription Flanking Active TSS Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
14	esv3421336	chr8:6421944-6427042	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Genic enhancers Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:48 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:6364200-6478200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr8:6416800-6442400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr8:6417600-6442800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr8:6419000-6462400	Weak transcription	GM12878-XiMat	blood
5	chr8:6420000-6427400	Weak transcription	Thymus	Thymus
6	chr8:6420800-6427600	Weak transcription	NHDF-Ad	bronchial
7	chr8:6420800-6429800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr8:6420800-6433200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr8:6421000-6425800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr8:6421000-6426000	Weak transcription	Stomach Smooth Muscle	stomach
11	chr8:6421000-6427400	Weak transcription	Left Ventricle	heart
12	chr8:6421000-6427400	Weak transcription	Ovary	ovary
13	chr8:6421000-6427800	Weak transcription	Aorta	Aorta
14	chr8:6421000-6427800	Weak transcription	Sigmoid Colon	Sigmoid Colon
15	chr8:6421000-6435400	Weak transcription	Muscle Satellite Cultured Cells	--
16	chr8:6421200-6436200	Weak transcription	Right Atrium	heart
17	chr8:6421400-6427400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr8:6421400-6433200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr8:6421600-6426800	Weak transcription	HUVEC	blood vessel
20	chr8:6421600-6462800	Weak transcription	Primary B cells from cord blood	blood
21	chr8:6421800-6427400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
22	chr8:6422000-6426800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr8:6424200-6442600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr8:6424400-6426000	Weak transcription	Fetal Muscle Trunk	muscle
25	chr8:6424400-6427000	Weak transcription	Adipose Nuclei	Adipose
26	chr8:6424400-6427000	Weak transcription	Skeletal Muscle Female	skeletal muscle
27	chr8:6424400-6434400	Weak transcription	Lung	lung
28	chr8:6424400-6442800	Weak transcription	NHEK	skin
29	chr8:6424600-6426000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr8:6424600-6433400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
31	chr8:6424800-6427600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr8:6424800-6430200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr8:6424800-6436600	Weak transcription	Esophagus	oesophagus
34	chr8:6424800-6440600	Weak transcription	Primary T cells from cord blood	blood
35	chr8:6424800-6442200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr8:6424800-6442600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr8:6424800-6451600	Weak transcription	Spleen	Spleen
38	chr8:6425000-6426800	Enhancers	Dnd41	blood
39	chr8:6425000-6427000	Weak transcription	Gastric	stomach
40	chr8:6425000-6427000	Weak transcription	Skeletal Muscle Male	skeletal muscle
41	chr8:6425000-6432800	Weak transcription	Pancreas	Pancrea
42	chr8:6425200-6427200	Weak transcription	Primary B cells from peripheral blood	blood
43	chr8:6425200-6429000	Enhancers	Primary hematopoietic stem cells	blood
44	chr8:6425200-6430200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr8:6425400-6426000	Weak transcription	Fetal Muscle Leg	muscle
46	chr8:6425400-6426000	Weak transcription	Fetal Thymus	thymus
47	chr8:6425400-6428400	Enhancers	Fetal Stomach	stomach
48	chr8:6425600-6427800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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