Variant report

Variant	rs59965458
Chromosome Location	chr7:87487034-87487035
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:87482216..87487472-chr7:87487902..87493572,9	K562	blood:
2	chr7:87484204..87488219-chr7:87489245..87493082,6	K562	blood:
3	chr7:87485338..87488263-chr7:87488457..87489975,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000075303	Chromatin interaction

Extended variants
information (count: 36 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs28381790	1.00[AMR][1000 genomes]
rs28381791	1.00[AMR][1000 genomes]
rs28381792	1.00[AMR][1000 genomes]
rs28381795	1.00[AMR][1000 genomes]
rs28381800	1.00[AMR][1000 genomes]
rs57593184	1.00[AMR][1000 genomes]
rs59075963	1.00[AMR][1000 genomes]
rs60521777	1.00[AMR][1000 genomes]
rs61056962	1.00[AMR][1000 genomes]
rs61232411	1.00[AMR][1000 genomes]
rs6950539	1.00[AMR][1000 genomes]
rs73705274	1.00[AMR][1000 genomes]
rs73705275	1.00[AMR][1000 genomes]
rs73706904	1.00[AFR][1000 genomes]
rs73706911	1.00[AFR][1000 genomes]
rs73706919	1.00[AFR][1000 genomes]
rs73706921	1.00[AFR][1000 genomes]
rs73706931	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73706933	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73706934	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73706936	1.00[AMR][1000 genomes]
rs73706937	1.00[AMR][1000 genomes]
rs73706938	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73706939	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73706943	1.00[AMR][1000 genomes]
rs73706945	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73706946	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73706947	1.00[AMR][1000 genomes]
rs73706949	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7801454	1.00[AMR][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	nsv888677	chr7:86802025-87781111	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
2	nsv464622	chr7:86832603-87541248	Weak transcription Flanking Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
3	nsv607725	chr7:86832603-87541248	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
4	nsv1015862	chr7:87075394-88049798	Bivalent/Poised TSS Flanking Active TSS Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
5	nsv1023352	chr7:87418818-88192925	Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
6	nsv539005	chr7:87418818-88192925	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:119 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:87460400-87487200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
2	chr7:87460600-87498000	Weak transcription	Fetal Heart	heart
3	chr7:87464000-87488400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
4	chr7:87464600-87487800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr7:87467200-87487200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr7:87467800-87494800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
7	chr7:87468400-87487200	Weak transcription	H1 Cell Line	embryonic stem cell
8	chr7:87468800-87489600	Strong transcription	Dnd41	blood
9	chr7:87469800-87491000	Weak transcription	Brain Angular Gyrus	brain
10	chr7:87470200-87499600	Weak transcription	NHEK	skin
11	chr7:87471000-87495600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
12	chr7:87471200-87495600	Weak transcription	Right Ventricle	heart
13	chr7:87471200-87499800	Weak transcription	NHLF	lung
14	chr7:87472200-87489200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr7:87472800-87489200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
16	chr7:87472800-87493600	Weak transcription	Esophagus	oesophagus
17	chr7:87473000-87493400	Weak transcription	H9 Cell Line	embryonic stem cell
18	chr7:87473200-87487200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr7:87473200-87495800	Weak transcription	Lung	lung
20	chr7:87474800-87487200	Weak transcription	Ovary	ovary
21	chr7:87474800-87488600	Weak transcription	Colonic Mucosa	Colon
22	chr7:87475000-87487200	Weak transcription	Brain Inferior Temporal Lobe	brain
23	chr7:87475000-87487400	Weak transcription	Brain Cingulate Gyrus	brain
24	chr7:87475000-87487400	Weak transcription	Rectal Smooth Muscle	rectum
25	chr7:87475000-87494800	Weak transcription	Pancreas	Pancrea
26	chr7:87475000-87495800	Weak transcription	Aorta	Aorta
27	chr7:87475000-87495800	Weak transcription	Spleen	Spleen
28	chr7:87475000-87500000	Weak transcription	Gastric	stomach
29	chr7:87475200-87495200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
30	chr7:87476000-87495200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr7:87477400-87488200	Weak transcription	Stomach Mucosa	stomach
32	chr7:87479200-87487200	Weak transcription	Brain Anterior Caudate	brain
33	chr7:87479200-87489600	Weak transcription	NHDF-Ad	bronchial
34	chr7:87480200-87494800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr7:87481000-87487400	Weak transcription	Thymus	Thymus
36	chr7:87481000-87487800	Weak transcription	Muscle Satellite Cultured Cells	--
37	chr7:87481000-87503800	Weak transcription	NH-A	brain
38	chr7:87481200-87504000	Weak transcription	Osteobl	bone
39	chr7:87481800-87487200	Weak transcription	Primary T cells from cord blood	blood
40	chr7:87482000-87487200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
41	chr7:87482000-87487200	Weak transcription	Fetal Muscle Trunk	muscle
42	chr7:87482000-87487400	Weak transcription	Fetal Intestine Small	intestine
43	chr7:87482000-87488600	Weak transcription	Fetal Brain Male	brain
44	chr7:87482200-87487200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
45	chr7:87482200-87488800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr7:87482200-87503200	Weak transcription	HMEC	breast
47	chr7:87482800-87494800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr7:87483000-87487600	Weak transcription	HepG2	liver
49	chr7:87483000-87489600	Strong transcription	Primary T helper cells fromperipheralblood	blood
50	chr7:87483200-87487200	Weak transcription	Fetal Lung	lung

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