Variant report

Variant	rs10977136
Chromosome Location	chr9:8471762-8471763
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 25 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10115800	1.00[MEX][hapmap]
rs10117452	1.00[MEX][hapmap];0.86[MKK][hapmap]
rs10120463	1.00[MEX][hapmap]
rs10121643	1.00[YRI][hapmap];0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10121790	1.00[MEX][hapmap]
rs10511495	0.83[YRI][hapmap];0.80[AFR][1000 genomes]
rs10977134	0.82[YRI][hapmap];0.85[AFR][1000 genomes]
rs10977138	1.00[TSI][hapmap]
rs10977139	0.87[AFR][1000 genomes]
rs10977166	1.00[MEX][hapmap]
rs12337324	1.00[ASW][hapmap];0.82[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.87[AFR][1000 genomes]
rs12340876	1.00[MEX][hapmap]
rs12344148	1.00[MEX][hapmap]
rs12349550	1.00[MEX][hapmap]
rs12352210	0.83[YRI][hapmap];0.80[AFR][1000 genomes]
rs7026937	1.00[TSI][hapmap]
rs7038093	1.00[TSI][hapmap]
rs7846893	1.00[TSI][hapmap]
rs7863545	1.00[CHD][hapmap]
rs9299065	0.83[YRI][hapmap];0.80[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 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	nsv613289	chr9:8456020-8473169	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:39 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:8418200-8476000	Weak transcription	Fetal Brain Male	brain
2	chr9:8419200-8491000	Weak transcription	Rectal Mucosa Donor 31	rectum
3	chr9:8420600-8557600	Weak transcription	Aorta	Aorta
4	chr9:8424200-8485000	Weak transcription	Fetal Kidney	kidney
5	chr9:8434200-8485200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr9:8442200-8522200	Weak transcription	Liver	Liver
7	chr9:8448000-8494800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr9:8448400-8472800	Weak transcription	Fetal Stomach	stomach
9	chr9:8451400-8492000	Weak transcription	Psoas Muscle	Psoas
10	chr9:8452400-8475800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr9:8453800-8476200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr9:8458200-8472000	Weak transcription	Fetal Heart	heart
13	chr9:8459000-8476000	Weak transcription	Cortex derived primary cultured neurospheres	brain
14	chr9:8460200-8473200	Weak transcription	Brain Angular Gyrus	brain
15	chr9:8460400-8475600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr9:8460600-8476000	Weak transcription	HUES64 Cell Line	embryonic stem cell
17	chr9:8462400-8472800	Weak transcription	Dnd41	blood
18	chr9:8462800-8472400	Weak transcription	Sigmoid Colon	Sigmoid Colon
19	chr9:8464600-8494200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr9:8465400-8475800	Weak transcription	Fetal Muscle Leg	muscle
21	chr9:8465600-8482600	Weak transcription	Rectal Mucosa Donor 29	rectum
22	chr9:8465800-8484000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr9:8468400-8472200	Weak transcription	Brain Cingulate Gyrus	brain
24	chr9:8468400-8478000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
25	chr9:8468600-8474200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
26	chr9:8468600-8484000	Weak transcription	Ovary	ovary
27	chr9:8470400-8473000	Weak transcription	Brain Hippocampus Middle	brain
28	chr9:8470800-8476200	Weak transcription	Fetal Lung	lung
29	chr9:8471000-8472200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr9:8471000-8472800	Weak transcription	Brain Substantia Nigra	brain
31	chr9:8471000-8475800	Weak transcription	Fetal Brain Female	brain
32	chr9:8471000-8477600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr9:8471000-8479200	Weak transcription	Brain Inferior Temporal Lobe	brain
34	chr9:8471200-8472800	Weak transcription	Brain Anterior Caudate	brain
35	chr9:8471200-8473200	Weak transcription	Primary hematopoietic stem cells	blood
36	chr9:8471200-8474400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr9:8471200-8476000	Weak transcription	Brain Germinal Matrix	brain
38	chr9:8471200-8476000	Weak transcription	Fetal Muscle Trunk	muscle
39	chr9:8471400-8476000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links