Variant report

Variant	rs521464
Chromosome Location	chr11:63523838-63523839
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:63522435..63525089-chr11:63529331..63531365,3	K562	blood:

Extended variants
information (count: 107 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:103)

rs_ID	r²[population]
rs10501394	1.00[CEU][hapmap];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11231535	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11231543	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11231545	1.00[CEU][hapmap]
rs11551942	1.00[CEU][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11551944	0.91[CEU][hapmap];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11820129	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1186941	1.00[CEU][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1211688	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12274980	1.00[CEU][hapmap];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17158453	1.00[CEU][hapmap];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17656941	1.00[CEU][hapmap];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1789219	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2509744	1.00[CEU][hapmap];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2959876	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2959880	1.00[CEU][hapmap];0.83[YRI][hapmap];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2959881	0.84[EUR][1000 genomes]
rs2959886	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs3016865	1.00[CEU][hapmap];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34109368	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35345497	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35754698	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs476034	1.00[CEU][hapmap];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs476691	1.00[CEU][hapmap];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs482915	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs484619	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs491231	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs500726	0.98[EUR][1000 genomes]
rs500991	1.00[CEU][hapmap];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs511819	1.00[CEU][hapmap];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs515645	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs517700	1.00[CEU][hapmap];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs518490	1.00[CEU][hapmap];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs518692	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs523093	1.00[CEU][hapmap];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs523809	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs534505	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs534876	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs539306	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs541809	0.92[EUR][1000 genomes]
rs550629	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs551466	1.00[CEU][hapmap];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs557882	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs559405	0.94[EUR][1000 genomes]
rs560938	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs562549	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs566813	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs567756	1.00[CEU][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs568769	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs568790	1.00[CEU][hapmap];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs580695	1.00[CEU][hapmap];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs588523	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61928162	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61928163	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61928165	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61928166	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61928167	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61928168	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61928195	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61928196	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61928197	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61928202	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61928203	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61928204	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61928205	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61928206	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61928208	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61928209	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61928211	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61928212	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61928214	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61928234	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61928236	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61928237	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61928238	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61928239	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61928241	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61928243	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61928244	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61928245	0.93[EUR][1000 genomes]
rs61928246	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61928247	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61928248	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61929731	0.81[EUR][1000 genomes]
rs6591821	0.95[EUR][1000 genomes]
rs6591822	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7106670	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7111395	1.00[CEU][hapmap];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7117206	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7119961	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7127454	1.00[CEU][hapmap];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7128040	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7128970	1.00[CEU][hapmap];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7928900	1.00[CEU][hapmap];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7931908	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7932117	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7939940	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7943981	1.00[CEU][hapmap];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7944003	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7944094	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7945972	1.00[CEU][hapmap];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7949389	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7949447	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]

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	nsv1051171	chr11:62987064-63835715	Genic enhancers Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	100 gene(s)	inside rSNPs	diseases
2	nsv832183	chr11:63416678-63564565	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
3	nsv468589	chr11:63515752-63713239	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
4	nsv555180	chr11:63515752-63713239	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:63473000-63529400	Weak transcription	Right Ventricle	heart
2	chr11:63491000-63529600	Weak transcription	Pancreas	Pancrea
3	chr11:63492800-63528000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr11:63501800-63530000	Weak transcription	Psoas Muscle	Psoas
5	chr11:63506200-63527600	Weak transcription	Fetal Brain Male	brain
6	chr11:63509000-63534800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
7	chr11:63511000-63534800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
8	chr11:63511200-63529800	Weak transcription	Stomach Mucosa	stomach
9	chr11:63512000-63524800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
10	chr11:63513600-63528400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr11:63513800-63529200	Weak transcription	Fetal Heart	heart
12	chr11:63514400-63528400	Strong transcription	Primary monocytes fromperipheralblood	blood
13	chr11:63514400-63528800	Strong transcription	Monocytes-CD14+_RO01746	blood
14	chr11:63515000-63529800	Weak transcription	Pancreatic Islets	Pancreatic Islet
15	chr11:63515400-63527200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
16	chr11:63515800-63527600	Weak transcription	Fetal Lung	lung
17	chr11:63515800-63529200	Strong transcription	Primary neutrophils fromperipheralblood	blood
18	chr11:63516000-63534800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
19	chr11:63516400-63527400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr11:63516400-63528400	Strong transcription	Adipose Nuclei	Adipose
21	chr11:63516400-63533400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr11:63516400-63534200	Weak transcription	Primary B cells from peripheral blood	blood
23	chr11:63516600-63527400	Strong transcription	HUES6 Cell Line	embryonic stem cell
24	chr11:63516600-63527400	Strong transcription	HUES64 Cell Line	embryonic stem cell
25	chr11:63516600-63527400	Strong transcription	iPS-18 Cell Line	embryonic stem cell
26	chr11:63516600-63528600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr11:63516600-63533800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
28	chr11:63516800-63530000	Weak transcription	Esophagus	oesophagus
29	chr11:63517000-63525800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr11:63517000-63527600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
31	chr11:63517200-63527400	Strong transcription	HUES48 Cell Line	embryonic stem cell
32	chr11:63517400-63530000	Weak transcription	Placenta Amnion	Placenta Amnion
33	chr11:63518400-63526600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr11:63518600-63526800	Strong transcription	Hela-S3	cervix
35	chr11:63518800-63524000	Weak transcription	Primary T helper cells PMA-I stimulated	--
36	chr11:63518800-63527600	Weak transcription	H9 Cell Line	embryonic stem cell
37	chr11:63518800-63530000	Weak transcription	Aorta	Aorta
38	chr11:63519200-63527600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
39	chr11:63519400-63528000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr11:63519400-63534800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
41	chr11:63520200-63527400	Weak transcription	Thymus	Thymus
42	chr11:63520400-63524000	Weak transcription	Gastric	stomach
43	chr11:63520400-63527400	Weak transcription	NHLF	lung
44	chr11:63520400-63533400	Weak transcription	GM12878-XiMat	blood
45	chr11:63520600-63524600	Weak transcription	Primary T cells from cord blood	blood
46	chr11:63520600-63528000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr11:63520800-63524800	Weak transcription	Primary T cells fromperipheralblood	blood
48	chr11:63520800-63524800	Weak transcription	Duodenum Mucosa	Duodenum
49	chr11:63520800-63525400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr11:63520800-63526000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood

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