Variant report

Variant	rs597591
Chromosome Location	chr18:25582289-25582290
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 75 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:71)

rs_ID	r²[population]
rs10502507	0.82[CHB][hapmap]
rs1078501	0.94[CHB][hapmap];0.88[CHD][hapmap]
rs10853680	0.82[CHB][hapmap]
rs10853681	0.82[CHB][hapmap]
rs1122356	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs1148376	0.94[CHB][hapmap];0.83[CHD][hapmap]
rs11564297	0.94[CHB][hapmap];0.88[CHD][hapmap]
rs11564316	0.94[CHB][hapmap];0.88[CHD][hapmap]
rs11564330	0.82[CHB][hapmap]
rs11564332	0.82[CHB][hapmap]
rs11564396	0.88[CHB][hapmap];0.83[CHD][hapmap]
rs11564400	0.94[CHB][hapmap]
rs11564409	0.94[CHB][hapmap];0.86[JPT][hapmap]
rs11564412	0.82[CHB][hapmap]
rs11564413	0.82[CHB][hapmap]
rs11873053	0.94[CHB][hapmap]
rs1220015	0.88[CHB][hapmap]
rs1220016	0.88[CHB][hapmap]
rs1220146	0.82[CEU][hapmap];0.81[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs1228419	0.88[CHB][hapmap];0.81[CHD][hapmap]
rs1234682	0.94[CHB][hapmap]
rs1238755	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1373136	0.94[CHB][hapmap]
rs1373138	0.88[CHB][hapmap]
rs1443450	0.82[CHB][hapmap]
rs1443453	0.82[CHB][hapmap]
rs17446001	0.82[CHB][hapmap]
rs17463233	0.82[CHB][hapmap]
rs17468531	0.94[CHB][hapmap]
rs17468636	0.82[CHB][hapmap]
rs1816825	1.00[CHB][hapmap];0.86[CHD][hapmap]
rs1867285	0.82[CHB][hapmap]
rs1941180	0.80[CHB][hapmap]
rs1972934	0.82[CHB][hapmap]
rs2053599	0.82[CHB][hapmap]
rs2218361	0.82[CHB][hapmap]
rs2920447	0.87[CHB][hapmap];0.81[JPT][hapmap]
rs4598992	0.82[CHB][hapmap]
rs4800838	0.82[CHB][hapmap]
rs4800840	1.00[CHB][hapmap]
rs4800841	0.82[CHB][hapmap]
rs490820	1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs500643	1.00[CHB][hapmap];0.86[CHD][hapmap]
rs533602	0.94[CHB][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs539075	0.84[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs565509	1.00[CHB][hapmap]
rs568575	0.94[CHB][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs576467	0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs584936	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap];0.97[AMR][1000 genomes];0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs587526	0.88[CHB][hapmap]
rs587613	0.94[CHB][hapmap]
rs602819	0.94[CHB][hapmap]
rs614966	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];0.82[LWK][hapmap];0.94[MKK][hapmap];1.00[TSI][hapmap];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs623234	0.82[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.89[TSI][hapmap];0.87[AMR][1000 genomes];0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs643555	0.81[CEU][hapmap];0.94[CHB][hapmap];0.97[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.98[TSI][hapmap];0.88[AMR][1000 genomes];0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs647733	1.00[CHB][hapmap]
rs656642	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs665651	0.94[CHB][hapmap]
rs665781	0.85[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.89[TSI][hapmap];0.89[AMR][1000 genomes];0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs673008	1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs694943	1.00[CHB][hapmap]
rs7230771	0.94[CHB][hapmap];0.88[CHD][hapmap]
rs7237382	0.88[CHB][hapmap]
rs8087457	0.82[CEU][hapmap];0.81[CHB][hapmap];0.88[CHD][hapmap];0.86[GIH][hapmap];0.95[JPT][hapmap];0.93[TSI][hapmap];0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs8087860	0.94[CHB][hapmap];0.83[CHD][hapmap]
rs8091314	0.88[CHB][hapmap]
rs8091763	0.82[CHB][hapmap]
rs8092004	0.82[CHB][hapmap]
rs9635986	0.87[CHB][hapmap]
rs9789154	1.00[CHB][hapmap]
rs9789221	0.82[CHB][hapmap]

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	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
2	nsv1066192	chr18:25454413-25606736	Weak transcription Flanking Active TSS Strong transcription Active TSS Enhancers Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
3	nsv543669	chr18:25454413-25606736	Enhancers Genic enhancers Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
4	nsv833605	chr18:25467096-25643447	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:55 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:25531200-25593600	Weak transcription	Fetal Kidney	kidney
2	chr18:25545600-25588600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr18:25553000-25593600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr18:25556200-25586800	Weak transcription	Spleen	Spleen
5	chr18:25556200-25592800	Weak transcription	Aorta	Aorta
6	chr18:25556200-25595800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr18:25556400-25584600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr18:25558800-25583600	Weak transcription	Right Ventricle	heart
9	chr18:25564800-25591400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
10	chr18:25565000-25592800	Weak transcription	A549	lung
11	chr18:25565200-25591800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr18:25566400-25584600	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr18:25571600-25588800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr18:25572800-25589800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr18:25573000-25590000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr18:25573600-25582400	Weak transcription	Brain Substantia Nigra	brain
17	chr18:25573600-25591200	Weak transcription	HUES48 Cell Line	embryonic stem cell
18	chr18:25573600-25593400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
19	chr18:25574800-25582800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
20	chr18:25574800-25584800	Weak transcription	HSMMtube	muscle
21	chr18:25575000-25582800	Weak transcription	Brain Angular Gyrus	brain
22	chr18:25575600-25591400	Weak transcription	H1 Cell Line	embryonic stem cell
23	chr18:25576400-25583800	Strong transcription	Liver	Liver
24	chr18:25577000-25591000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr18:25577200-25583200	Strong transcription	HSMM	muscle
26	chr18:25577200-25583800	Weak transcription	Fetal Lung	lung
27	chr18:25577400-25582800	Strong transcription	Osteobl	bone
28	chr18:25577400-25583000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr18:25577400-25583400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr18:25577600-25583000	Strong transcription	NH-A	brain
31	chr18:25577600-25589800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
32	chr18:25577800-25585200	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr18:25578000-25583600	Strong transcription	HUES6 Cell Line	embryonic stem cell
34	chr18:25578200-25582600	Strong transcription	Fetal Brain Female	brain
35	chr18:25578200-25582600	Strong transcription	Dnd41	blood
36	chr18:25578200-25583200	Strong transcription	Brain Germinal Matrix	brain
37	chr18:25578200-25591400	Strong transcription	HUES64 Cell Line	embryonic stem cell
38	chr18:25579000-25584000	Weak transcription	Fetal Brain Male	brain
39	chr18:25579200-25583800	Weak transcription	Brain Anterior Caudate	brain
40	chr18:25579200-25591400	Weak transcription	HepG2	liver
41	chr18:25579400-25583000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr18:25580600-25582800	Weak transcription	Muscle Satellite Cultured Cells	--
43	chr18:25580600-25593400	Weak transcription	Ovary	ovary
44	chr18:25580600-25595800	Weak transcription	Left Ventricle	heart
45	chr18:25580800-25589600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr18:25581200-25582600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr18:25581800-25586400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr18:25582000-25582400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
49	chr18:25582000-25582400	Enhancers	Brain Cingulate Gyrus	brain
50	chr18:25582000-25583600	Strong transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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