Variant report

Variant	rs7241766
Chromosome Location	chr18:13517327-13517328
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr18:13504939..13506992-chr18:13515304..13518121,2	MCF-7	breast:

Extended variants
information (count: 63 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:61)

rs_ID	r²[population]
rs10163734	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10853235	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10853236	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs12458741	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][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]
rs12604898	0.82[JPT][hapmap]
rs12607174	0.87[JPT][hapmap];0.80[ASN][1000 genomes]
rs12955640	0.86[CHB][hapmap];0.84[CHD][hapmap];0.94[JPT][hapmap];0.80[MEX][hapmap];0.94[ASN][1000 genomes]
rs1648585	0.86[CHB][hapmap];0.84[CHD][hapmap];0.94[JPT][hapmap];0.80[MEX][hapmap];0.94[ASN][1000 genomes]
rs1648586	0.85[CHB][hapmap];0.94[JPT][hapmap];0.94[ASN][1000 genomes]
rs1648587	0.86[CHB][hapmap];0.84[CHD][hapmap];0.81[GIH][hapmap];0.94[JPT][hapmap];0.94[ASN][1000 genomes]
rs1648588	0.85[CHB][hapmap];0.81[JPT][hapmap];0.80[ASN][1000 genomes]
rs1648593	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1785151	0.86[CHB][hapmap];0.93[JPT][hapmap];0.94[ASN][1000 genomes]
rs1785152	0.85[CHB][hapmap];0.88[JPT][hapmap];0.94[ASN][1000 genomes]
rs1785181	0.86[CHB][hapmap];0.83[JPT][hapmap]
rs1785205	0.86[CHB][hapmap];0.84[CHD][hapmap];0.94[JPT][hapmap];0.80[MEX][hapmap];0.94[ASN][1000 genomes]
rs1812468	0.82[JPT][hapmap]
rs1940914	0.80[ASN][1000 genomes]
rs1940915	0.80[ASN][1000 genomes]
rs1940916	0.81[CHD][hapmap];0.88[JPT][hapmap];0.80[MEX][hapmap];0.80[ASN][1000 genomes]
rs1940918	0.80[ASN][1000 genomes]
rs2027682	0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2027683	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.96[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]
rs2163445	0.81[ASN][1000 genomes]
rs28415200	0.80[ASN][1000 genomes]
rs28553871	0.80[ASN][1000 genomes]
rs28767549	0.80[ASN][1000 genomes]
rs3097643	0.84[CHD][hapmap];0.88[JPT][hapmap];0.80[ASN][1000 genomes]
rs3132835	0.84[CHD][hapmap];0.88[JPT][hapmap];0.80[MEX][hapmap];0.80[ASN][1000 genomes]
rs3859302	0.87[AFR][1000 genomes];0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4121593	0.82[JPT][hapmap]
rs4121594	0.80[JPT][hapmap]
rs4796988	0.84[CHD][hapmap];0.88[JPT][hapmap];0.80[ASN][1000 genomes]
rs6505818	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6505819	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6505820	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6505821	1.00[CEU][hapmap];0.89[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6505822	0.94[ASW][hapmap];1.00[CEU][hapmap];0.83[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7227383	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7229109	0.83[CHB][hapmap];0.80[ASN][1000 genomes]
rs7230189	1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7230276	1.00[CEU][hapmap];0.89[GIH][hapmap];1.00[TSI][hapmap];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7233826	0.80[ASN][1000 genomes]
rs7234676	0.80[ASN][1000 genomes]
rs7239669	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7240391	0.84[CHD][hapmap];0.88[JPT][hapmap];0.80[ASN][1000 genomes]
rs7240795	0.80[ASN][1000 genomes]
rs7240821	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7240858	0.84[CHD][hapmap];0.88[JPT][hapmap];0.85[MEX][hapmap];0.80[ASN][1000 genomes]
rs7241010	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7505922	0.80[ASN][1000 genomes]
rs8088361	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8091197	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8091352	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[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]
rs8092166	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9952307	0.88[JPT][hapmap];0.80[ASN][1000 genomes]
rs9958211	0.80[ASN][1000 genomes]
rs9958308	0.80[ASN][1000 genomes]
rs9958406	0.80[ASN][1000 genomes]
rs9958516	0.80[ASN][1000 genomes]
rs9958760	0.80[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531246	chr18:13298774-14082028	Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
2	esv1827877	chr18:13511622-13523462	Strong transcription Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:60 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:13471000-13537400	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr18:13499600-13539200	Weak transcription	Gastric	stomach
3	chr18:13499800-13531000	Weak transcription	Rectal Mucosa Donor 29	rectum
4	chr18:13500400-13517400	Weak transcription	Spleen	Spleen
5	chr18:13501400-13518200	Weak transcription	Duodenum Smooth Muscle	Duodenum
6	chr18:13501600-13525000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr18:13501800-13530600	Weak transcription	Rectal Smooth Muscle	rectum
8	chr18:13502800-13525200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
9	chr18:13503000-13519200	Weak transcription	Pancreas	Pancrea
10	chr18:13503200-13521000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
11	chr18:13503400-13517400	Weak transcription	Aorta	Aorta
12	chr18:13505000-13536000	Weak transcription	Rectal Mucosa Donor 31	rectum
13	chr18:13507000-13536400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
14	chr18:13511600-13530400	Weak transcription	Colon Smooth Muscle	Colon
15	chr18:13512000-13518200	Weak transcription	Brain Hippocampus Middle	brain
16	chr18:13512200-13521600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
17	chr18:13512800-13518400	Strong transcription	Dnd41	blood
18	chr18:13513200-13520000	Weak transcription	Brain Cingulate Gyrus	brain
19	chr18:13513200-13526600	Weak transcription	Brain Inferior Temporal Lobe	brain
20	chr18:13513200-13538200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
21	chr18:13513400-13523800	Weak transcription	Primary T helper cells PMA-I stimulated	--
22	chr18:13513600-13517600	Strong transcription	Primary T helper cells fromperipheralblood	blood
23	chr18:13513600-13517600	Weak transcription	Fetal Intestine Large	intestine
24	chr18:13513600-13519400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
25	chr18:13513800-13520200	Strong transcription	Primary T cells from cord blood	blood
26	chr18:13513800-13520200	Weak transcription	Left Ventricle	heart
27	chr18:13514000-13520000	Weak transcription	Fetal Heart	heart
28	chr18:13514000-13520200	Weak transcription	Psoas Muscle	Psoas
29	chr18:13514000-13523800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
30	chr18:13514200-13517800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr18:13514200-13519200	Strong transcription	Monocytes-CD14+_RO01746	blood
32	chr18:13514400-13519000	Strong transcription	Primary T cells fromperipheralblood	blood
33	chr18:13514600-13517800	Strong transcription	Primary neutrophils fromperipheralblood	blood
34	chr18:13515400-13520200	Weak transcription	Right Atrium	heart
35	chr18:13515600-13517600	Strong transcription	Primary B cells from cord blood	blood
36	chr18:13515600-13519000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr18:13515600-13520000	Weak transcription	Skeletal Muscle Female	skeletal muscle
38	chr18:13515600-13521000	Weak transcription	Brain Anterior Caudate	brain
39	chr18:13516000-13517400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
40	chr18:13516000-13517600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
41	chr18:13516000-13517800	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
42	chr18:13516200-13517400	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
43	chr18:13516200-13517600	Strong transcription	Primary B cells from peripheral blood	blood
44	chr18:13516200-13517600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
45	chr18:13516200-13519400	Strong transcription	Liver	Liver
46	chr18:13516400-13517600	ZNF genes & repeats	Fetal Thymus	thymus
47	chr18:13516600-13517600	Strong transcription	Stomach Smooth Muscle	stomach
48	chr18:13516600-13517800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
49	chr18:13516800-13517600	Strong transcription	Duodenum Mucosa	Duodenum
50	chr18:13516800-13517600	Strong transcription	Skeletal Muscle Male	skeletal muscle

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links