Variant report

Variant	rs12336978
Chromosome Location	chr9:73568337-73568338
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs10116690	0.89[EUR][1000 genomes]
rs10120894	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10123027	0.89[EUR][1000 genomes]
rs10511993	0.81[AMR][1000 genomes]
rs12342244	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12343924	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12347867	0.96[EUR][1000 genomes]
rs28697055	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs56095958	0.81[AMR][1000 genomes]
rs56226184	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs73647180	0.89[EUR][1000 genomes]
rs73647181	0.89[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv893441	chr9:73486034-73594114	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
2	nsv430072	chr9:73509677-73640530	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:29 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:73563000-73569000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
2	chr9:73563600-73568600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr9:73563800-73568600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr9:73563800-73568600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr9:73563800-73568600	Weak transcription	HMEC	breast
6	chr9:73563800-73568600	Weak transcription	NHEK	skin
7	chr9:73564000-73569200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr9:73565800-73568400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr9:73566600-73568600	Enhancers	Osteobl	bone
10	chr9:73566600-73568800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr9:73566600-73570800	Enhancers	NHDF-Ad	bronchial
12	chr9:73566800-73570400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr9:73567000-73571000	Enhancers	HSMM	muscle
14	chr9:73567000-73571000	Enhancers	HSMMtube	muscle
15	chr9:73567200-73568600	Weak transcription	Aorta	Aorta
16	chr9:73567200-73570000	Enhancers	Muscle Satellite Cultured Cells	--
17	chr9:73567200-73571200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr9:73567400-73568400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr9:73567600-73568600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr9:73567600-73568600	Enhancers	NH-A	brain
21	chr9:73567600-73568600	Enhancers	NHLF	lung
22	chr9:73567600-73569000	Weak transcription	Fetal Heart	heart
23	chr9:73567600-73569800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr9:73568000-73568400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
25	chr9:73568000-73568400	Weak transcription	Placenta	Placenta
26	chr9:73568000-73568400	Weak transcription	Placenta Amnion	Placenta Amnion
27	chr9:73568000-73570000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr9:73568200-73568600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr9:73568200-73571400	Enhancers	HUES64 Cell Line	embryonic stem cell

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