Variant report

Variant	rs10758977
Chromosome Location	chr9:8504101-8504102
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10114195	0.91[CEU][hapmap];0.81[AMR][1000 genomes]
rs10114412	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10117986	0.92[CEU][hapmap];0.94[GIH][hapmap];0.90[MEX][hapmap];0.92[TSI][hapmap];0.81[AMR][1000 genomes]
rs10119236	0.88[CEU][hapmap];0.82[TSI][hapmap]
rs10511497	0.92[CEU][hapmap]
rs10511498	0.87[CEU][hapmap];0.90[EUR][1000 genomes]
rs10758976	0.96[CEU][hapmap];0.81[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10815885	0.92[CEU][hapmap];0.94[GIH][hapmap];0.95[MEX][hapmap];0.95[TSI][hapmap];0.89[EUR][1000 genomes]
rs10815886	0.86[CEU][hapmap]
rs10815887	0.91[CEU][hapmap]
rs10977149	0.96[CEU][hapmap];0.84[EUR][1000 genomes]
rs12341185	0.96[CEU][hapmap];0.84[EUR][1000 genomes]
rs1998516	0.87[LWK][hapmap];0.82[TSI][hapmap];0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2296101	1.00[CEU][hapmap];0.83[GIH][hapmap];0.90[MEX][hapmap];0.95[TSI][hapmap];0.88[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs2381803	0.87[CEU][hapmap];0.80[GIH][hapmap];0.84[TSI][hapmap]
rs2381804	0.96[CEU][hapmap];0.90[MEX][hapmap];0.90[TSI][hapmap];0.84[EUR][1000 genomes]
rs2381805	0.96[CEU][hapmap];0.80[AMR][1000 genomes]
rs2890796	0.96[CEU][hapmap]
rs4324967	0.91[CEU][hapmap]
rs6477311	1.00[CEU][hapmap];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6477312	0.92[CEU][hapmap];0.82[CHB][hapmap];0.83[GIH][hapmap];1.00[MEX][hapmap];0.86[TSI][hapmap];0.83[YRI][hapmap];0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7035558	1.00[CEU][hapmap];0.95[CHB][hapmap];0.81[CHD][hapmap];0.86[GIH][hapmap];0.83[JPT][hapmap];0.89[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.80[YRI][hapmap];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs746106	0.92[CEU][hapmap]
rs767674	0.96[CEU][hapmap];0.80[AMR][1000 genomes]
rs767675	0.92[CEU][hapmap];0.91[GIH][hapmap];0.90[MEX][hapmap];0.87[TSI][hapmap];0.84[AMR][1000 genomes]
rs7854860	0.81[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv8414	chr9:7827373-8511613	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	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
3	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
4	nsv892226	chr9:8435525-8522326	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	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
6	nsv892229	chr9:8485201-8520366	Weak transcription Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	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
8	nsv613290	chr9:8501698-8514338	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:43 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:8420600-8557600	Weak transcription	Aorta	Aorta
2	chr9:8442200-8522200	Weak transcription	Liver	Liver
3	chr9:8483800-8524800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr9:8486000-8508400	Weak transcription	Brain Cingulate Gyrus	brain
5	chr9:8486000-8519400	Weak transcription	Cortex derived primary cultured neurospheres	brain
6	chr9:8486000-8522200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
7	chr9:8486200-8504600	Weak transcription	Sigmoid Colon	Sigmoid Colon
8	chr9:8486200-8509000	Weak transcription	Brain Anterior Caudate	brain
9	chr9:8486200-8517200	Weak transcription	Fetal Muscle Trunk	muscle
10	chr9:8486200-8522800	Weak transcription	Rectal Mucosa Donor 29	rectum
11	chr9:8486200-8523200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr9:8486200-8531600	Weak transcription	Fetal Kidney	kidney
13	chr9:8486600-8507200	Weak transcription	Brain Inferior Temporal Lobe	brain
14	chr9:8487000-8521200	Weak transcription	Brain Germinal Matrix	brain
15	chr9:8487000-8521200	Weak transcription	Dnd41	blood
16	chr9:8492400-8504200	Weak transcription	H9 Cell Line	embryonic stem cell
17	chr9:8492400-8528800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr9:8493000-8518000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr9:8493000-8521200	Weak transcription	Fetal Muscle Leg	muscle
20	chr9:8493200-8523200	Weak transcription	Fetal Stomach	stomach
21	chr9:8493200-8531200	Weak transcription	Fetal Brain Female	brain
22	chr9:8494200-8531200	Weak transcription	Fetal Brain Male	brain
23	chr9:8494600-8506800	Weak transcription	Brain Hippocampus Middle	brain
24	chr9:8495000-8507000	Weak transcription	Brain Substantia Nigra	brain
25	chr9:8495000-8517800	Weak transcription	Ovary	ovary
26	chr9:8495600-8520400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr9:8499800-8517600	Weak transcription	Primary hematopoietic stem cells	blood
28	chr9:8500600-8516800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr9:8501000-8504400	Weak transcription	Rectal Mucosa Donor 31	rectum
30	chr9:8501000-8509000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr9:8501000-8517600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr9:8501200-8517200	Weak transcription	Fetal Lung	lung
33	chr9:8501600-8517000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr9:8503200-8504400	Enhancers	iPS-18 Cell Line	embryonic stem cell
35	chr9:8503400-8504400	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr9:8503400-8504400	Enhancers	iPS-20b Cell Line	embryonic stem cell
37	chr9:8503600-8504200	Enhancers	HUES6 Cell Line	embryonic stem cell
38	chr9:8503600-8504400	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr9:8503600-8504400	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr9:8504000-8504200	Genic enhancers	Brain Angular Gyrus	brain
41	chr9:8504000-8504400	Enhancers	ES-I3 Cell Line	embryonic stem cell
42	chr9:8504000-8504400	Enhancers	H1 Cell Line	embryonic stem cell
43	chr9:8504000-8504400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell

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