Variant report

Variant	rs11135482
Chromosome Location	chr5:96221426-96221427
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 122 )
Associated
traits (count: 16 )

rSNPs within LD-proxies of this variant (count:113)

rs_ID	r²[population]
rs10071975	0.91[CHB][hapmap];0.95[JPT][hapmap]
rs1019503	0.91[CHB][hapmap];0.95[JPT][hapmap];0.83[ASN][1000 genomes]
rs10434708	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10434709	1.00[ASW][hapmap];1.00[CHB][hapmap];0.98[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.99[MKK][hapmap];0.93[TSI][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1056893	0.95[CHB][hapmap];0.90[CHD][hapmap];0.86[GIH][hapmap];0.95[JPT][hapmap];0.89[YRI][hapmap];0.86[ASN][1000 genomes]
rs11135483	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11135484	0.94[ASW][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];0.95[LWK][hapmap];0.95[MKK][hapmap];0.93[TSI][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]
rs11135485	0.81[ASN][1000 genomes]
rs11750025	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1216565	0.95[CHB][hapmap];0.95[JPT][hapmap];0.82[YRI][hapmap];0.84[ASN][1000 genomes]
rs1216569	0.84[ASN][1000 genomes]
rs1216570	0.83[ASN][1000 genomes]
rs12189125	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1230381	0.83[ASN][1000 genomes]
rs1230382	0.83[ASN][1000 genomes]
rs12516666	1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12653964	0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12654015	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12655858	0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12716486	0.90[CHB][hapmap];1.00[JPT][hapmap]
rs13167902	1.00[ASW][hapmap];0.95[CHB][hapmap];0.86[CHD][hapmap];0.89[GIH][hapmap];0.95[JPT][hapmap];1.00[LWK][hapmap];0.94[MKK][hapmap];0.93[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs13189819	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1363975	0.83[ASN][1000 genomes]
rs1363977	0.83[ASN][1000 genomes]
rs1423357	0.82[YRI][hapmap]
rs1423568	0.86[ASN][1000 genomes]
rs1559354	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1559355	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1559357	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs17087165	0.86[ASN][1000 genomes]
rs171647	0.86[ASN][1000 genomes]
rs187265	0.95[CHB][hapmap];0.95[JPT][hapmap];0.89[YRI][hapmap];0.86[ASN][1000 genomes]
rs193993	0.87[ASN][1000 genomes]
rs1974871	1.00[CHB][hapmap];0.98[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];0.93[TSI][hapmap]
rs1981846	1.00[CHB][hapmap];0.86[CHD][hapmap];0.80[GIH][hapmap];0.91[JPT][hapmap];0.84[ASN][1000 genomes]
rs2042383	0.87[ASN][1000 genomes]
rs2042385	0.91[CHB][hapmap];0.95[JPT][hapmap];0.83[ASN][1000 genomes]
rs2113189	0.91[YRI][hapmap];0.87[ASN][1000 genomes]
rs2113190	0.86[ASN][1000 genomes]
rs2113191	0.86[ASN][1000 genomes]
rs2161657	0.95[CHB][hapmap];0.91[CHD][hapmap];0.95[JPT][hapmap];0.86[ASN][1000 genomes]
rs2161658	0.95[CHB][hapmap];0.95[JPT][hapmap];0.89[YRI][hapmap];0.86[ASN][1000 genomes]
rs2247650	0.95[CHB][hapmap];0.95[JPT][hapmap];0.89[YRI][hapmap];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2248374	0.86[ASN][1000 genomes]
rs2255546	0.91[CHB][hapmap];0.91[CHD][hapmap];0.87[GIH][hapmap];0.95[JPT][hapmap];0.89[YRI][hapmap];0.83[ASN][1000 genomes]
rs2255633	0.91[CHB][hapmap];0.95[JPT][hapmap];0.89[YRI][hapmap];0.83[ASN][1000 genomes]
rs2255634	0.91[CHB][hapmap];0.95[JPT][hapmap];0.89[YRI][hapmap];0.83[ASN][1000 genomes]
rs2255637	0.91[CHB][hapmap];0.95[JPT][hapmap];0.89[YRI][hapmap];0.83[ASN][1000 genomes]
rs2278018	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2278019	1.00[ASW][hapmap];1.00[CHB][hapmap];0.98[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.99[MKK][hapmap];0.93[TSI][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2287988	0.95[CHB][hapmap];0.91[CHD][hapmap];0.87[GIH][hapmap];0.95[JPT][hapmap];0.89[YRI][hapmap];0.86[ASN][1000 genomes]
rs248215	0.86[CHB][hapmap];0.95[JPT][hapmap]
rs251342	0.86[ASN][1000 genomes]
rs251344	0.95[CHB][hapmap];0.95[JPT][hapmap];0.81[ASN][1000 genomes]
rs2548521	0.81[ASN][1000 genomes]
rs2548522	0.83[ASN][1000 genomes]
rs2548523	0.90[CHB][hapmap];0.95[JPT][hapmap];0.89[YRI][hapmap];0.86[ASN][1000 genomes]
rs2548524	0.91[CHB][hapmap];0.95[JPT][hapmap];0.89[YRI][hapmap];0.86[ASN][1000 genomes]
rs2548526	0.86[ASN][1000 genomes]
rs2548527	0.95[CHB][hapmap];0.91[CHD][hapmap];0.87[GIH][hapmap];0.95[JPT][hapmap];0.86[ASN][1000 genomes]
rs2548528	0.86[ASN][1000 genomes]
rs2548529	0.86[ASN][1000 genomes]
rs2548533	0.95[CHB][hapmap];0.91[CHD][hapmap];0.87[GIH][hapmap];0.95[JPT][hapmap];0.89[YRI][hapmap];0.86[ASN][1000 genomes]
rs2548534	0.87[ASN][1000 genomes]
rs2548535	0.87[ASN][1000 genomes]
rs2548536	0.95[CHB][hapmap];0.95[JPT][hapmap];0.91[YRI][hapmap];0.87[ASN][1000 genomes]
rs2548537	0.95[CHB][hapmap];0.95[JPT][hapmap];0.93[YRI][hapmap];0.87[ASN][1000 genomes]
rs2548538	0.95[CHB][hapmap];0.95[JPT][hapmap];0.89[YRI][hapmap];0.87[ASN][1000 genomes]
rs2548539	0.95[CHB][hapmap];0.95[JPT][hapmap];0.88[YRI][hapmap];0.87[ASN][1000 genomes]
rs2548540	0.95[CHB][hapmap];0.95[JPT][hapmap];0.89[YRI][hapmap];0.87[ASN][1000 genomes]
rs2549781	0.95[CHB][hapmap];0.95[JPT][hapmap];0.87[ASN][1000 genomes]
rs2549782	0.91[CHB][hapmap];0.88[CHD][hapmap];0.86[GIH][hapmap];0.95[JPT][hapmap];0.89[YRI][hapmap];0.87[ASN][1000 genomes]
rs2549784	0.87[ASN][1000 genomes]
rs2549785	0.95[CHB][hapmap];0.91[CHD][hapmap];0.87[GIH][hapmap];0.95[JPT][hapmap];0.89[YRI][hapmap];0.87[ASN][1000 genomes]
rs2549787	0.86[ASN][1000 genomes]
rs2549788	0.86[ASN][1000 genomes]
rs2549789	0.86[ASN][1000 genomes]
rs2549790	0.95[CHB][hapmap];0.95[JPT][hapmap];0.89[YRI][hapmap];0.86[ASN][1000 genomes]
rs2549791	0.95[CHB][hapmap];0.95[JPT][hapmap];0.86[ASN][1000 genomes]
rs2549792	0.84[ASN][1000 genomes]
rs2549795	0.95[CHB][hapmap];0.91[CHD][hapmap];0.87[GIH][hapmap];0.95[JPT][hapmap];0.89[YRI][hapmap];0.86[ASN][1000 genomes]
rs2549796	0.95[CHB][hapmap];0.90[CHD][hapmap];0.95[JPT][hapmap];0.86[ASN][1000 genomes]
rs2549797	0.95[CHB][hapmap];0.91[CHD][hapmap];0.87[GIH][hapmap];0.95[JPT][hapmap];0.89[YRI][hapmap];0.86[ASN][1000 genomes]
rs2549800	0.82[ASN][1000 genomes]
rs2549801	0.83[ASN][1000 genomes]
rs27397	0.91[CHB][hapmap];0.91[CHD][hapmap];0.95[JPT][hapmap]
rs27747	0.91[CHB][hapmap];0.95[JPT][hapmap]
rs2910686	0.89[CHB][hapmap];0.90[JPT][hapmap];0.84[YRI][hapmap];0.82[ASN][1000 genomes]
rs2910688	0.81[ASN][1000 genomes]
rs33934033	0.86[ASN][1000 genomes]
rs3734015	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs38035	0.91[CHB][hapmap];0.95[JPT][hapmap]
rs38036	0.90[CHB][hapmap];0.95[JPT][hapmap]
rs38041	0.91[CHB][hapmap];0.95[JPT][hapmap]
rs38042	0.82[JPT][hapmap]
rs3849750	0.95[CHB][hapmap];0.95[JPT][hapmap];0.87[ASN][1000 genomes]
rs4869311	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4869312	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4869313	0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4869314	0.95[CHB][hapmap];0.91[JPT][hapmap];0.80[YRI][hapmap];0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4869315	0.84[ASW][hapmap];0.96[YRI][hapmap]
rs55770741	0.82[EUR][1000 genomes]
rs56197090	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6556942	0.83[EUR][1000 genomes]
rs6556943	0.87[ASN][1000 genomes]
rs6859160	0.86[ASN][1000 genomes]
rs6868302	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6873441	0.86[ASN][1000 genomes]
rs6874656	0.87[ASN][1000 genomes]
rs7700332	0.91[CHB][hapmap];0.95[JPT][hapmap]
rs7713127	0.91[CHB][hapmap];0.95[JPT][hapmap];0.81[ASN][1000 genomes]
rs7721944	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7736466	0.91[CHB][hapmap];0.91[CHD][hapmap];0.95[JPT][hapmap];0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv432755	chr5:95987984-96657483	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
2	nsv598962	chr5:96057891-96893164	Weak transcription Strong transcription Enhancers Bivalent/Poised TSS Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
3	nsv948703	chr5:96078309-96368839	Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
4	nsv1027472	chr5:96081592-96337550	Strong transcription Genic enhancers Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
5	nsv1028741	chr5:96082401-96372165	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
6	nsv949058	chr5:96082433-96390619	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
7	nsv598963	chr5:96084776-96363407	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
8	nsv432756	chr5:96113844-96234644	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
9	nsv531967	chr5:96127842-96302702	Flanking Active TSS Strong transcription Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases

mRNA abundance (count:16)

SNP	Gene	Cis/trans	Tissue	Source
rs11135482	ERAP2	cis	Muscle Skeletal	GTEx
rs11135482	LNPEP	cis	brain	seeQTL
rs11135482	ERAP2	cis	Thyroid	GTEx
rs11135482	ERAP2	cis	lung	GTEx
rs11135482	ERAP2	cis	Artery Aorta	GTEx
rs11135482	ERAP2	cis	Stomach	GTEx
rs11135482	ERAP2	cis	Esophagus Muscularis	GTEx
rs11135482	ERAP2	cis	Skin Sun Exposed Lower leg	GTEx
rs11135482	AC008865.1	cis	Artery Tibial	GTEx
rs11135482	ERAP2	cis	Nerve Tibial	GTEx
rs11135482	ERAP2	cis	Adipose Subcutaneous	GTEx
rs11135482	ERAP2	cis	Artery Tibial	GTEx
rs11135482	ERAP2	cis	Whole Blood	GTEx
rs11135482	LNPEP	trans	brain	seeQTL
rs11135482	ERAP2	cis	Esophagus Mucosa	GTEx
rs11135482	ERAP2	cis	Heart Left Ventricle	GTEx

Chromatin state (count:98 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:96212600-96232000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr5:96213000-96239000	Weak transcription	Pancreas	Pancrea
3	chr5:96213200-96221600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
4	chr5:96213200-96225200	Weak transcription	Ovary	ovary
5	chr5:96213200-96229200	Weak transcription	Aorta	Aorta
6	chr5:96213400-96221600	Weak transcription	Brain Angular Gyrus	brain
7	chr5:96213400-96223600	Weak transcription	Fetal Kidney	kidney
8	chr5:96213400-96237800	Weak transcription	Brain Substantia Nigra	brain
9	chr5:96213400-96243800	Weak transcription	HepG2	liver
10	chr5:96213400-96247000	Weak transcription	Fetal Lung	lung
11	chr5:96215400-96222400	Genic enhancers	Fetal Thymus	thymus
12	chr5:96217200-96222600	Genic enhancers	Primary B cells from peripheral blood	blood
13	chr5:96217400-96221800	Genic enhancers	Dnd41	blood
14	chr5:96217400-96229200	Weak transcription	Colonic Mucosa	Colon
15	chr5:96217600-96228800	Weak transcription	HSMM	muscle
16	chr5:96217600-96241600	Weak transcription	Primary neutrophils fromperipheralblood	blood
17	chr5:96217600-96250000	Weak transcription	Fetal Muscle Trunk	muscle
18	chr5:96217800-96224600	Weak transcription	Rectal Smooth Muscle	rectum
19	chr5:96217800-96225200	Weak transcription	Gastric	stomach
20	chr5:96217800-96228800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr5:96217800-96229200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr5:96217800-96229200	Weak transcription	Muscle Satellite Cultured Cells	--
23	chr5:96217800-96237800	Weak transcription	NHDF-Ad	bronchial
24	chr5:96218000-96221600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr5:96218000-96222600	Genic enhancers	Primary T cells fromperipheralblood	blood
26	chr5:96218000-96222600	Genic enhancers	Primary T helper cells fromperipheralblood	blood
27	chr5:96218000-96222600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr5:96218000-96225200	Weak transcription	Spleen	Spleen
29	chr5:96218000-96229000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr5:96218000-96229000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr5:96218000-96229200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr5:96218000-96237000	Weak transcription	NHLF	lung
33	chr5:96218000-96264600	Weak transcription	Right Ventricle	heart
34	chr5:96218200-96222200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr5:96218200-96228600	Weak transcription	NH-A	brain
36	chr5:96218200-96228800	Weak transcription	NHEK	skin
37	chr5:96218200-96231400	Weak transcription	Colon Smooth Muscle	Colon
38	chr5:96218200-96232000	Weak transcription	Brain Anterior Caudate	brain
39	chr5:96218200-96237000	Weak transcription	Hela-S3	cervix
40	chr5:96218400-96224600	Weak transcription	Fetal Heart	heart
41	chr5:96218600-96259600	Weak transcription	HMEC	breast
42	chr5:96218800-96221800	Strong transcription	Fetal Intestine Large	intestine
43	chr5:96218800-96228600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr5:96219000-96222200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr5:96219000-96222600	Genic enhancers	Primary T regulatory cells fromperipheralblood	blood
46	chr5:96219600-96221600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr5:96220000-96221600	Genic enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
48	chr5:96220000-96222400	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
49	chr5:96220200-96222400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
50	chr5:96220400-96221600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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