Variant report

Variant	rs17536472
Chromosome Location	chr18:25715757-25715758
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs10853682	1.00[JPT][hapmap]
rs11083249	1.00[JPT][hapmap]
rs11083250	1.00[JPT][hapmap]
rs11083252	1.00[JPT][hapmap]
rs11564299	1.00[JPT][hapmap]
rs11564310	1.00[CEU][hapmap];1.00[JPT][hapmap];0.85[YRI][hapmap]
rs11564336	1.00[CEU][hapmap];1.00[JPT][hapmap];0.85[YRI][hapmap]
rs11564341	1.00[JPT][hapmap]
rs11564381	1.00[CEU][hapmap];1.00[JPT][hapmap]
rs11872284	1.00[JPT][hapmap]
rs11874384	1.00[CEU][hapmap];1.00[JPT][hapmap];0.82[YRI][hapmap]
rs11874478	1.00[JPT][hapmap]
rs12185349	1.00[JPT][hapmap]
rs12454164	1.00[JPT][hapmap]
rs12457737	1.00[JPT][hapmap]
rs12457781	1.00[JPT][hapmap]
rs12458418	1.00[JPT][hapmap]
rs12953509	1.00[JPT][hapmap]
rs12956036	1.00[JPT][hapmap]
rs12959867	1.00[JPT][hapmap]
rs12960181	1.00[JPT][hapmap]
rs1443449	1.00[JPT][hapmap]
rs17446505	1.00[JPT][hapmap]
rs17446547	1.00[JPT][hapmap]
rs17446875	1.00[JPT][hapmap]
rs17468924	1.00[JPT][hapmap]
rs17469001	1.00[JPT][hapmap]
rs17469371	1.00[JPT][hapmap]
rs1860642	1.00[CEU][hapmap];1.00[JPT][hapmap];0.82[YRI][hapmap]
rs1944288	1.00[JPT][hapmap]
rs2067772	1.00[JPT][hapmap]
rs2191636	1.00[JPT][hapmap]
rs4800289	1.00[JPT][hapmap]
rs4800842	1.00[JPT][hapmap]
rs6508526	1.00[JPT][hapmap]
rs719723	1.00[JPT][hapmap]
rs8089347	1.00[JPT][hapmap]
rs8091862	1.00[JPT][hapmap]
rs8095341	1.00[JPT][hapmap]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2761996	chr18:24866083-25818618	Flanking Active TSS Enhancers Strong transcription Weak transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:25696200-25727800	Weak transcription	HSMMtube	muscle
2	chr18:25696600-25715800	Weak transcription	HUVEC	blood vessel
3	chr18:25703800-25727600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr18:25703800-25730000	Weak transcription	Aorta	Aorta
5	chr18:25705000-25727800	Weak transcription	Ovary	ovary
6	chr18:25705200-25727400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr18:25708800-25719200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr18:25708800-25721400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr18:25709000-25719600	Weak transcription	Osteobl	bone
10	chr18:25709000-25724400	Weak transcription	HUES64 Cell Line	embryonic stem cell
11	chr18:25709200-25715800	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr18:25709400-25727600	Weak transcription	A549	lung
13	chr18:25710200-25727600	Weak transcription	HepG2	liver
14	chr18:25710400-25726400	Weak transcription	HUES48 Cell Line	embryonic stem cell
15	chr18:25710400-25726400	Weak transcription	Fetal Brain Female	brain
16	chr18:25710400-25727600	Weak transcription	Brain Anterior Caudate	brain
17	chr18:25710400-25727600	Weak transcription	Brain Substantia Nigra	brain
18	chr18:25710600-25725000	Weak transcription	HUES6 Cell Line	embryonic stem cell
19	chr18:25710600-25727400	Weak transcription	Brain Inferior Temporal Lobe	brain
20	chr18:25710600-25731000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
21	chr18:25712600-25728400	Weak transcription	Right Ventricle	heart
22	chr18:25712600-25730000	Weak transcription	Left Ventricle	heart
23	chr18:25712800-25728400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr18:25713000-25722000	Weak transcription	Brain Cingulate Gyrus	brain
25	chr18:25713000-25725000	Weak transcription	Liver	Liver
26	chr18:25713000-25727400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr18:25713200-25719800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr18:25713200-25720200	Weak transcription	Cortex derived primary cultured neurospheres	brain
29	chr18:25713400-25716800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr18:25713800-25716000	Genic enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr18:25713800-25716200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr18:25713800-25724600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr18:25714400-25716400	Enhancers	Fetal Heart	heart
34	chr18:25714600-25716400	Strong transcription	HSMM	muscle
35	chr18:25714800-25716400	Strong transcription	Muscle Satellite Cultured Cells	--
36	chr18:25714800-25716400	Genic enhancers	NH-A	brain
37	chr18:25714800-25727600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
38	chr18:25715000-25719600	Weak transcription	Brain Germinal Matrix	brain
39	chr18:25715600-25717600	Enhancers	Dnd41	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links