Variant report

Variant	rs59101086
Chromosome Location	chr18:45533509-45533510
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr18:45529545..45532435-chr18:45532709..45536356,5	MCF-7	breast:
2	chr18:45459837..45461431-chr18:45533159..45534772,2	MCF-7	breast:
3	chr18:45529640..45533731-chr18:45547574..45549695,3	MCF-7	breast:
4	chr18:45454989..45458191-chr18:45533485..45536799,4	MCF-7	breast:
5	chr18:45528601..45531772-chr18:45533301..45535605,3	K562	blood:

Variant related genes	Relation type
ENSG00000175387	Chromatin interaction

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs57868878	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs57913684	0.89[EUR][1000 genomes]
rs57959928	0.89[EUR][1000 genomes]
rs59002988	0.89[EUR][1000 genomes]
rs7226472	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs73445907	0.89[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv909616	chr18:45467806-45844500	Active TSS Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv1066479	chr18:45505569-45554507	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv1055669	chr18:45513090-45559375	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Strong transcription	Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:52 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:45530400-45534200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
2	chr18:45530400-45534200	Weak transcription	Duodenum Smooth Muscle	Duodenum
3	chr18:45530400-45534200	Weak transcription	Psoas Muscle	Psoas
4	chr18:45530400-45534400	Weak transcription	Aorta	Aorta
5	chr18:45530400-45534400	Weak transcription	Fetal Heart	heart
6	chr18:45530600-45534000	Weak transcription	Adipose Nuclei	Adipose
7	chr18:45530600-45534000	Weak transcription	Fetal Kidney	kidney
8	chr18:45530600-45534000	Weak transcription	Left Ventricle	heart
9	chr18:45530600-45534000	Weak transcription	Lung	lung
10	chr18:45530600-45534200	Weak transcription	Skeletal Muscle Female	skeletal muscle
11	chr18:45530600-45534200	Weak transcription	Stomach Mucosa	stomach
12	chr18:45530600-45534400	Weak transcription	Gastric	stomach
13	chr18:45530600-45534400	Weak transcription	Placenta Amnion	Placenta Amnion
14	chr18:45530600-45534400	Weak transcription	Sigmoid Colon	Sigmoid Colon
15	chr18:45530800-45533800	Weak transcription	Spleen	Spleen
16	chr18:45530800-45534000	Weak transcription	Pancreas	Pancrea
17	chr18:45530800-45534000	Weak transcription	Right Ventricle	heart
18	chr18:45530800-45534000	Weak transcription	Skeletal Muscle Male	skeletal muscle
19	chr18:45530800-45534200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr18:45530800-45534200	Weak transcription	Duodenum Mucosa	Duodenum
21	chr18:45530800-45534200	Weak transcription	Rectal Mucosa Donor 31	rectum
22	chr18:45531000-45534000	Weak transcription	NH-A	brain
23	chr18:45531000-45534200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr18:45531000-45534200	Weak transcription	Muscle Satellite Cultured Cells	--
25	chr18:45531000-45534200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr18:45531000-45534200	Weak transcription	HSMMtube	muscle
27	chr18:45531000-45534400	Enhancers	Hela-S3	cervix
28	chr18:45531200-45533800	Weak transcription	Fetal Muscle Leg	muscle
29	chr18:45531200-45533800	Weak transcription	Placenta	Placenta
30	chr18:45531200-45534000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr18:45531200-45534000	Weak transcription	HSMM	muscle
32	chr18:45531200-45534000	Weak transcription	HUVEC	blood vessel
33	chr18:45531200-45534200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
34	chr18:45531200-45534200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr18:45531200-45534200	Weak transcription	Right Atrium	heart
36	chr18:45531200-45534200	Weak transcription	Thymus	Thymus
37	chr18:45531200-45534400	Weak transcription	Primary hematopoietic stem cells	blood
38	chr18:45531200-45534400	Weak transcription	Small Intestine	intestine
39	chr18:45531400-45533800	Weak transcription	Dnd41	blood
40	chr18:45531400-45534200	Weak transcription	HMEC	breast
41	chr18:45533000-45534000	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
42	chr18:45533000-45534000	Enhancers	A549	lung
43	chr18:45533000-45534200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr18:45533000-45534400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr18:45533200-45533600	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
46	chr18:45533200-45534200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr18:45533200-45534200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
48	chr18:45533200-45534200	Enhancers	Fetal Thymus	thymus
49	chr18:45533400-45533600	Enhancers	Primary hematopoietic stem cells short term culture	blood
50	chr18:45533400-45534000	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell

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