Variant report

Variant	rs10758978
Chromosome Location	chr9:8528506-8528507
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

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

rs_ID	r²[population]
rs10117042	0.86[ASN][1000 genomes]
rs10120190	0.86[ASN][1000 genomes]
rs10123125	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10123138	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10124867	0.87[ASN][1000 genomes]
rs10511499	0.80[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs10758979	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10758980	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10815896	0.86[ASN][1000 genomes]
rs10815898	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10815900	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10815905	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10815906	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10815907	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10815908	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10977169	0.84[ASN][1000 genomes]
rs10977170	0.86[ASN][1000 genomes]
rs10977181	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10977189	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10977192	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10977196	0.91[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12340211	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12341045	0.84[ASN][1000 genomes]
rs12341078	0.85[ASN][1000 genomes]
rs12344975	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12350641	0.80[AFR][1000 genomes]
rs1998513	0.85[ASN][1000 genomes]
rs1998515	0.86[ASN][1000 genomes]
rs2273998	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3763652	0.82[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs3763653	0.96[ASN][1000 genomes]
rs6477313	0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1031472	chr9:8250901-8712547	Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
2	nsv1022796	chr9:8360729-9110046	Enhancers Weak transcription Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
3	nsv892228	chr9:8482778-8703733	Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
4	nsv831504	chr9:8496277-8665773	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA target site	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:24 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:8420600-8557600	Weak transcription	Aorta	Aorta
2	chr9:8486200-8531600	Weak transcription	Fetal Kidney	kidney
3	chr9:8492400-8528800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr9:8493200-8531200	Weak transcription	Fetal Brain Female	brain
5	chr9:8494200-8531200	Weak transcription	Fetal Brain Male	brain
6	chr9:8509400-8528600	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr9:8509800-8532800	Weak transcription	Brain Angular Gyrus	brain
8	chr9:8518000-8528600	Weak transcription	Rectal Mucosa Donor 31	rectum
9	chr9:8518400-8533800	Weak transcription	Primary hematopoietic stem cells	blood
10	chr9:8518400-8534000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr9:8518400-8555200	Weak transcription	Fetal Muscle Trunk	muscle
12	chr9:8519800-8531600	Weak transcription	HUES48 Cell Line	embryonic stem cell
13	chr9:8520000-8531200	Weak transcription	Cortex derived primary cultured neurospheres	brain
14	chr9:8522000-8528600	Weak transcription	Brain Germinal Matrix	brain
15	chr9:8522200-8531400	Weak transcription	Brain Cingulate Gyrus	brain
16	chr9:8522400-8529200	Weak transcription	Brain Anterior Caudate	brain
17	chr9:8522400-8530800	Weak transcription	Fetal Muscle Leg	muscle
18	chr9:8522400-8531600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr9:8524200-8531600	Weak transcription	Brain Substantia Nigra	brain
20	chr9:8525000-8531600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr9:8525000-8533200	Weak transcription	Fetal Lung	lung
22	chr9:8525400-8528800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr9:8526200-8531800	Weak transcription	HUES64 Cell Line	embryonic stem cell
24	chr9:8528400-8528800	Weak transcription	Brain Hippocampus Middle	brain

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