Variant report

Variant	rs11874384
Chromosome Location	chr18:25712314-25712315
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 46 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs10853682	1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11083249	1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11083250	1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11083252	1.00[JPT][hapmap]
rs11564299	1.00[JPT][hapmap]
rs11564310	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11564336	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11564341	1.00[JPT][hapmap]
rs11564381	1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11872284	1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11874478	1.00[JPT][hapmap]
rs12185349	1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12453985	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12454164	0.91[GIH][hapmap];1.00[JPT][hapmap];0.82[LWK][hapmap];1.00[MEX][hapmap];0.86[TSI][hapmap];0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12454769	0.90[ASN][1000 genomes]
rs12457737	1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12457781	1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12458418	1.00[JPT][hapmap]
rs12458840	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12458872	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12953509	0.91[GIH][hapmap];1.00[JPT][hapmap];0.88[LWK][hapmap];1.00[MEX][hapmap];0.92[MKK][hapmap];0.86[TSI][hapmap];0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12956036	1.00[JPT][hapmap]
rs12959867	1.00[JPT][hapmap]
rs12960181	1.00[JPT][hapmap]
rs12969129	0.90[ASN][1000 genomes]
rs1443449	0.91[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.86[TSI][hapmap];0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs17446505	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs17446547	1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs17446875	1.00[JPT][hapmap]
rs17468924	1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs17468987	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs17469001	1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs17469371	1.00[JPT][hapmap]
rs17536472	1.00[CEU][hapmap];1.00[JPT][hapmap];0.82[YRI][hapmap]
rs1860642	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.96[LWK][hapmap];1.00[MEX][hapmap];0.95[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1944288	1.00[JPT][hapmap]
rs2067772	1.00[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.93[MEX][hapmap];0.92[MKK][hapmap];0.86[TSI][hapmap];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2191636	1.00[JPT][hapmap]
rs4800289	1.00[JPT][hapmap]
rs4800842	1.00[JPT][hapmap];0.83[AFR][1000 genomes];0.96[AMR][1000 genomes];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6508526	1.00[JPT][hapmap]
rs719723	1.00[JPT][hapmap]
rs8089347	1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs8091862	1.00[JPT][hapmap]
rs8095341	1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]

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:44 , 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	chr18:25697800-25715600	Weak transcription	Dnd41	blood
4	chr18:25703800-25727600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr18:25703800-25730000	Weak transcription	Aorta	Aorta
6	chr18:25705000-25727800	Weak transcription	Ovary	ovary
7	chr18:25705200-25727400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr18:25706600-25713000	Enhancers	Brain Germinal Matrix	brain
9	chr18:25706800-25713200	Enhancers	Fetal Heart	heart
10	chr18:25708800-25714600	Weak transcription	HSMM	muscle
11	chr18:25708800-25719200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr18:25708800-25721400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr18:25709000-25714800	Weak transcription	Muscle Satellite Cultured Cells	--
14	chr18:25709000-25719600	Weak transcription	Osteobl	bone
15	chr18:25709000-25724400	Weak transcription	HUES64 Cell Line	embryonic stem cell
16	chr18:25709200-25715800	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr18:25709400-25713200	Enhancers	Cortex derived primary cultured neurospheres	brain
18	chr18:25709400-25727600	Weak transcription	A549	lung
19	chr18:25710200-25727600	Weak transcription	HepG2	liver
20	chr18:25710400-25712400	Weak transcription	Brain Angular Gyrus	brain
21	chr18:25710400-25726400	Weak transcription	HUES48 Cell Line	embryonic stem cell
22	chr18:25710400-25726400	Weak transcription	Fetal Brain Female	brain
23	chr18:25710400-25727600	Weak transcription	Brain Anterior Caudate	brain
24	chr18:25710400-25727600	Weak transcription	Brain Substantia Nigra	brain
25	chr18:25710600-25725000	Weak transcription	HUES6 Cell Line	embryonic stem cell
26	chr18:25710600-25727400	Weak transcription	Brain Inferior Temporal Lobe	brain
27	chr18:25710600-25731000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
28	chr18:25710800-25712800	Weak transcription	Brain Cingulate Gyrus	brain
29	chr18:25710800-25714800	Weak transcription	NH-A	brain
30	chr18:25711400-25712400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr18:25711600-25712800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr18:25711800-25712600	Enhancers	Left Ventricle	heart
33	chr18:25711800-25713000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr18:25711800-25713000	Genic enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr18:25711800-25713000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
36	chr18:25711800-25713200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr18:25711800-25713800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr18:25712000-25712600	Enhancers	Fetal Intestine Small	intestine
39	chr18:25712000-25712600	Enhancers	Right Ventricle	heart
40	chr18:25712000-25712800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr18:25712000-25712800	Enhancers	Right Atrium	heart
42	chr18:25712000-25713000	Enhancers	Liver	Liver
43	chr18:25712200-25712600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
44	chr18:25712200-25712600	Enhancers	Fetal Intestine Large	intestine

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