Variant report

Variant	rs72745079
Chromosome Location	chr9:86047910-86047911
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr9:86046084..86048921-chr9:86138267..86141242,2	MCF-7	breast:
2	chr9:86046794..86050465-chr9:86050692..86054566,4	MCF-7	breast:

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs17086243	0.95[ASN][1000 genomes]
rs17086262	1.00[ASN][1000 genomes]
rs17086263	1.00[ASN][1000 genomes]
rs3860920	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3860922	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3860923	1.00[ASN][1000 genomes]
rs55723059	0.86[AFR][1000 genomes]
rs60581387	0.97[ASN][1000 genomes]
rs72745063	1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72745065	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72745066	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72745068	0.86[AFR][1000 genomes]
rs72745070	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72745075	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72745077	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72745085	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72745088	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72745094	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs72745098	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs72745100	0.86[AFR][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	nsv1046491	chr9:85861492-86063992	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv893512	chr9:86022215-86323309	Flanking Active TSS Bivalent Enhancer Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
3	nsv1048086	chr9:86040900-86059732	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:36 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:86039200-86050000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr9:86040400-86050000	Weak transcription	Fetal Intestine Large	intestine
3	chr9:86045600-86048200	Enhancers	Liver	Liver
4	chr9:86045800-86048000	Enhancers	NHDF-Ad	bronchial
5	chr9:86045800-86048200	Enhancers	Skeletal Muscle Male	skeletal muscle
6	chr9:86046200-86048600	Weak transcription	Gastric	stomach
7	chr9:86046600-86048000	Enhancers	Monocytes-CD14+_RO01746	blood
8	chr9:86046600-86050800	Enhancers	Primary monocytes fromperipheralblood	blood
9	chr9:86046800-86048000	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr9:86047200-86052200	Enhancers	Rectal Mucosa Donor 31	rectum
11	chr9:86047400-86048600	Weak transcription	Rectal Mucosa Donor 29	rectum
12	chr9:86047400-86049200	Weak transcription	Right Ventricle	heart
13	chr9:86047400-86049200	Weak transcription	Stomach Mucosa	stomach
14	chr9:86047400-86050400	Enhancers	HepG2	liver
15	chr9:86047400-86052600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr9:86047400-86056600	Weak transcription	Stomach Smooth Muscle	stomach
17	chr9:86047400-86059000	Weak transcription	Placenta	Placenta
18	chr9:86047600-86048000	Weak transcription	Pancreas	Pancrea
19	chr9:86047600-86048600	Weak transcription	Adipose Nuclei	Adipose
20	chr9:86047600-86048600	Weak transcription	Left Ventricle	heart
21	chr9:86047600-86048600	Weak transcription	Lung	lung
22	chr9:86047600-86048600	Weak transcription	Psoas Muscle	Psoas
23	chr9:86047600-86048600	Weak transcription	Right Atrium	heart
24	chr9:86047600-86048600	Weak transcription	Skeletal Muscle Female	skeletal muscle
25	chr9:86047600-86048600	Weak transcription	Spleen	Spleen
26	chr9:86047600-86048800	Weak transcription	Sigmoid Colon	Sigmoid Colon
27	chr9:86047600-86049000	Weak transcription	Colonic Mucosa	Colon
28	chr9:86047600-86049400	Enhancers	Hela-S3	cervix
29	chr9:86047600-86051200	Weak transcription	Fetal Heart	heart
30	chr9:86047600-86052400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr9:86047600-86053800	Weak transcription	Aorta	Aorta
32	chr9:86047600-86055800	Weak transcription	Esophagus	oesophagus
33	chr9:86047600-86055800	Weak transcription	Ovary	ovary
34	chr9:86047600-86059200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr9:86047600-86062400	Weak transcription	Colon Smooth Muscle	Colon
36	chr9:86047800-86048000	Weak transcription	A549	lung

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